Manual de Servicio TEC-8300

SERVICE MANUAL
Defibrillator TEC-8321K/8322K/8332K/8342K/8352K Service Manual

Defibrillator
TEC-8321K/TEC-8322K
TEC-8332K/TEC-8342K
TEC-8352K
TEC-8300 series
First Edition: 05 Apr 2011

Seventh Edition: 11 Mar 2015
0634-900736F
Printed: 2015/04/03
Service Manual
Defibrillator
TEC-8321K/TEC-8322K
TEC-8332K/TEC-8342K
TEC-8352K
TEC-8300 series
0634-900736F
In order to use this product safely and fully understand all its functions, make sure to read this manual before using the
product.
Keep this manual near the instrument or in the reach of the operator and refer to it whenever the operation is unclear.
This product stores personal patient information. Manage and operate the information appropriately.
Patient names on the screen shots and recording examples in this manual are fictional and any resemblance to any
person living or dead is purely coincidental.
The contents of this manual are subject to change without notice.
If you have any comments or suggestions on this manual, please contact us at: www.nihonkohden.com
Copyright Notice
The entire contents of this manual are copyrighted by Nihon Kohden. All rights are reserved. No part of this document
may be reproduced, stored, or transmitted in any form or by any means (electronic, mechanical, photocopied, recorded,
or otherwise) without the prior written permission of Nihon Kohden.
Trademark
The mark printed on the SD card that is used in this instrument is a trademark.
Bluetooth® and its logo are trademarks of Bluetooth SIG, Inc.

1
Contents 2
GENERAL HANDLING PRECAUTIONS.............................................................................. i 3

WARRANTY POLICY.......................................................................................................... ii
EMC RELATED CAUTION...................................................................................................iii 4
Conventions Used in this Manual and Instrument............................................................... v
Warnings, Cautions and Notes.................................................................................. v 5
Related Documentation...................................................................................................... vi
Section 1 General.................................................................................... 1.1

Introduction....................................................................................................................... 1.3
Models and Functions............................................................................................ 1.3
Parameters............................................................................................................. 1.3
General Information on Servicing..................................................................................... 1.4
Service Policy, Service Parts and Patient Safety Checks................................................. 1.6
Service Policy......................................................................................................... 1.6
Service Parts.......................................................................................................... 1.6
Patient Safety Checks............................................................................................. 1.7
Maintenance Equipments and Tools....................................................................... 1.8
Specifications.................................................................................................................... 1.9
Defibrillator............................................................................................................. 1.9
Analysis Accuracy................................................................................................ 1.12
Monitor.................................................................................................................. 1.13
Alarm Delay Time................................................................................................. 1.13
Lead ECG............................................................................................................. 1.13
Paddle ECG.......................................................................................................... 1.13
External ECG........................................................................................................ 1.13
Recorder............................................................................................................... 1.14
Noninvasive Pacing (TEC-8332/TEC-8352 Only)................................................. 1.14
External Paddle (ND-831V).................................................................................. 1.14
ECG...................................................................................................................... 1.14
SpO2 .................................................................................................................... 1.14
CO2 ...................................................................................................................... 1.14
NIBP (TEC-8342/TEC-8352 only)........................................................................ 1.14
Invasive Blood Pressure....................................................................................... 1.15
Temperature......................................................................................................... 1.15
Alarm.................................................................................................................... 1.15
Battery.................................................................................................................. 1.16
AC Power Requirements...................................................................................... 1.16
Clock Accuracy..................................................................................................... 1.16
Environment......................................................................................................... 1.16
Dimensions and Weight........................................................................................ 1.16
Safety.................................................................................................................... 1.17
Environment Conditions........................................................................................ 1.17
Electromagnetic Compatibility.............................................................................. 1.18
Electromagnetic Emissions.................................................................................. 1.18
Service Manual TEC-8300 C.1

CONTENTS
Electromagnetic Immunity.................................................................................... 1.19

Recommended Separation Distances between Portable and Mobile RF
Communications Equipment................................................................................. 1.22
System Configuration for EMC Test...................................................................... 1.23
Panel Description............................................................................................................ 1.24
Front Panel........................................................................................................... 1.24
Right Side Panel................................................................................................... 1.25
Left Side Panel..................................................................................................... 1.26
Rear Panel............................................................................................................ 1.27
ND-831V External Paddles (Option)..................................................................... 1.28
ND-860V Series Internal Paddles (Option)........................................................... 1.29
ND-890V Series Internal Paddles (Option)........................................................... 1.29
Composition.................................................................................................................... 1.30
Standard Components.......................................................................................... 1.30
TEC-8321................................................................................................... 1.30
TEC-8322................................................................................................... 1.31
TEC-8332................................................................................................... 1.32
TEC-8342................................................................................................... 1.33
TEC-8352................................................................................................... 1.34
Options................................................................................................................. 1.35
Board and Unit Location................................................................................................. 1.37
Section 2 Troubleshooting..................................................................... 2.1

How to Troubleshoot......................................................................................................... 2.2
Error Code........................................................................................................................ 2.3
Defibrillation............................................................................................................ 2.4
Operation Panel...................................................................................................... 2.5
Communication....................................................................................................... 2.6
Data Error............................................................................................................... 2.7
Pacing (TEC-8332/TEC-8352 Only)....................................................................... 2.7
12 Lead ECG Measurement (When Using the Optional AC-831V 12 Lead ECG
Unit)........................................................................................................................ 2.8
Message........................................................................................................................... 2.9
Defibrillation and Cardioversion.............................................................................. 2.9
AED...................................................................................................................... 2.10
Pacing................................................................................................................... 2.10
Monitoring............................................................................................................. 2.11
ECG............................................................................................................ 2.11
SpO2 .......................................................................................................... 2.12
CO2 ............................................................................................................ 2.13
Invasive Blood Pressure............................................................................. 2.13
NIBP........................................................................................................... 2.13
Temperature............................................................................................... 2.14
System.................................................................................................................. 2.16
General....................................................................................................... 2.16
Battery........................................................................................................ 2.16
Recording................................................................................................... 2.17
Bluetooth.................................................................................................... 2.17
C.2 Service Manual TEC-8300

CONTENTS
Troubleshooting............................................................................................................... 2.18 1
General................................................................................................................. 2.18
Defibrillation.......................................................................................................... 2.19 2
Pacing (TEC-8332/TEC-8352 Only)..................................................................... 2.20
Monitoring............................................................................................................. 2.20 3
ECG............................................................................................................ 2.20
SpO2 .......................................................................................................... 2.21 4
CO2 ............................................................................................................ 2.22
NIBP........................................................................................................... 2.23 5
Blood Pressure (PRESS)........................................................................... 2.24
Temperature............................................................................................... 2.24
Recording............................................................................................................. 2.24
Battery.................................................................................................................. 2.25
SD Card................................................................................................................ 2.25
Section 3 Disassembly........................................................................... 3.1

Before You Begin............................................................................................................... 3.3
Warnings, Cautions and Notes............................................................................... 3.3
Registering Serial Number after Board Replacement............................................ 3.4
Required Tools........................................................................................................ 3.5
Connection Diagram......................................................................................................... 3.6
Removing the External Paddle Holder or Top Cover....................................................... 3.11
Removing the Optional 12 Lead ECG Unit..................................................................... 3.14
Removing the QI-831V AUXOUT Unit and QI-832V Bluetooth® Module........................ 3.16
Removing the Front Case............................................................................................... 3.19
Removing the LCD Unit and the LED DRIVER Board.................................................... 3.21
Removing the UR-0414 CONTROL Board and the UR-0415 ECG/PACER Board......... 3.23
Removing the HV-831V HV Unit and UR-0418 HV CPU Board..................................... 3.26
Note for Assembling the Defibrillator after HV Unit Replacement........................ 3.27
Removing the MP Unit.................................................................................................... 3.29
Removing the Input Enclosure............................................................................. 3.30
Removing the UR-0454 TEMP Board................................................................... 3.31
Removing the UR-0455 MP Board....................................................................... 3.32
Removing the UR-3908 SpO2 Board.................................................................... 3.33
Removing the UR-0444 ECG CONN1 Board....................................................... 3.33
Removing the UR-0445 ECG CONN2 Board....................................................... 3.34
Removing the NIBP Pump.................................................................................... 3.34
Removing the Valve.............................................................................................. 3.35
Removing the UR-0431 REC/EXT Board....................................................................... 3.36
Removing the Recorder Unit.......................................................................................... 3.37
Removing the UR-0417 Power Board............................................................................. 3.39
Removing the KEY/LED Boards..................................................................................... 3.42
Removing the Speaker................................................................................................... 3.44
Removing the Paddle Connector.................................................................................... 3.45

CONTENTS
Section 4 Maintenance........................................................................... 4.1

General............................................................................................................................. 4.4
Periodic Inspection................................................................................................. 4.4
Daily Inspection............................................................................................ 4.4
Monthly Inspection....................................................................................... 4.4
Yearly Inspection.......................................................................................... 4.4
Repair Parts Availability Policy............................................................................... 4.4
Before Check.................................................................................................................... 4.5
Recording and Saving the Reports......................................................................... 4.5
When Using a Loaner Defibrillator.......................................................................... 4.5
Copying the Settings to the Loaner Defibrillator........................................... 4.5
Checking the Appearance................................................................................................. 4.6
Checking the SB-831V Battery Pack................................................................................ 4.7
Checking the Defibrillator.................................................................................................. 4.8
Connecting the Checker and Turning the Defibrillator On...................................... 4.8
Adjusting the Sync Sound...................................................................................... 4.9
Checking the Recorder........................................................................................... 4.9
Record/Stop Key.......................................................................................... 4.9
Date and Time Printed on the Recording Paper........................................... 4.9
Event Key..................................................................................................... 4.9
Recording Quality......................................................................................... 4.9
Detecting Out of Paper............................................................................... 4.10
Checking the Defibrillation Function in Manual Mode..................................................... 4.11
Checking the Connector Off Detection................................................................. 4.11
Checking the Duration of Charging Energy.......................................................... 4.13
AC Power.................................................................................................... 4.13
Battery Power............................................................................................. 4.14
Checking the Discharged Waveform..................................................................... 4.15
Checking the Discharged Energy......................................................................... 4.19
AC Power.................................................................................................... 4.20
Battery Power............................................................................................. 4.20
Checking the Discharge for When Using the Disposable Pads............................ 4.21
Checking the Discharge for When Using the Internal Paddles............................. 4.22
Checking for Changing the Energy Setting After Charging is Complete.............. 4.22
Checking Internal Discharge................................................................................ 4.23
Checking the Synchronized Cardioversion..................................................................... 4.25
Checking the Synchronized Cardioversion Using the Paddle Lead...................... 4.25
Checking the Synchronized Cardioversion Using the ECG Lead......................... 4.27
Checking in the AED Mode............................................................................................. 4.30
Preparation........................................................................................................... 4.30
Checking ECG Analysis in AED Mode, Charge and Discharge........................... 4.30
Checking the Display............................................................................................ 4.32
Checking the Voice Instruction.............................................................................. 4.32
Checking the Pacing Function........................................................................................ 4.33
Preparation........................................................................................................... 4.33
Checking the Pacing in Fixed Mode..................................................................... 4.34
Checking the Pacing in Demand Mode................................................................ 4.35
Checking the Pacing Rate and Output Current.................................................... 4.37
Checking the Monitoring Parameters.............................................................................. 4.38

CONTENTS
Checking the Electrocardiogram (ECG)............................................................... 4.38 1

Preparations............................................................................................... 4.38
Checking the Accuracy of the Heart Rate and the Generation of 2
Synchronous Sound................................................................................... 4.39
Checking the Sensitivity of ECG................................................................. 4.39 3
Checking the Detection of the Heart Rate and Electrode-Off Alarms........ 4.40
Checking the IBP.................................................................................................. 4.41 4
Preparation................................................................................................. 4.41
Checking the Accuracy of Zero Calibration................................................ 4.41 5
Checking the Accuracy of the Blood Pressure Value................................. 4.42
Checking the Detection of an Connector-Off Alarm................................... 4.43
Checking the CO2 Value....................................................................................... 4.43
Preparation................................................................................................. 4.43
Checking the Accuracy of the Respiration Rate and the CO2 Value........... 4.43
Checking the Detection of an Connector-Off Alarm................................... 4.44
Checking the Measurement Accuracy of the CO2 Sensor Kit..................... 4.44
Preparations............................................................................................... 4.44
Checking the SpO2 Value...................................................................................... 4.49
Preparation................................................................................................. 4.49
Checking the Accuracy of the SpO2 Value and the Pulse Rate.................. 4.50
Checking the Detection of Alarm for the SpO2 Value and a Connector-Off
Alarm.......................................................................................................... 4.50
Checking the NIBP (TEC-8342/8352 Only).......................................................... 4.51
Preparation................................................................................................. 4.51
Checking the Type of the Connected Cuff.................................................. 4.51
Checking the Measurement Operation and Display of Measured Value.... 4.51
Checking the Measurement Stop Function................................................ 4.51
Checking the Temperature.................................................................................... 4.52
Preparations............................................................................................... 4.52
Check the Accuracy of Temperature........................................................... 4.53
Checking the Connector-Off Detection....................................................... 4.53
Checking the Sensor-Off Detection............................................................ 4.53
Checking the AC-831V 12 Lead ECG Unit..................................................................... 4.54
Preparations......................................................................................................... 4.54
Checking the 12 Lead ECG Display..................................................................... 4.55
Checking the Connector-Off Detection....................................................... 4.55
Safety Check................................................................................................................... 4.56
External Paddles and Internal Paddles................................................................. 4.58
Pad Adapter.......................................................................................................... 4.58
ECG (Electrode Lead).......................................................................................... 4.58
SpO2 Probe........................................................................................................... 4.58
Checking the SB-801V Battery Charger......................................................................... 4.59
Inspection Items................................................................................................... 4.59
Safety Check........................................................................................................ 4.60
System Maintenance Screen.......................................................................................... 4.61
Displaying the System Maintenance Screen........................................................ 4.61
Saving the Settings before Maintenance (Flash Save Procedure)....................... 4.62
Changing the Settings to Factory Default............................................................. 4.63
About the Menu Items.......................................................................................... 4.64

CONTENTS
System Maintenance Screen Flowchart..................................................... 4.64

Default Settings.......................................................................................... 4.65
Configuration Screen............................................................................................ 4.66
Adjust AD Screen................................................................................................. 4.67
Adjust ECG A/D Screen............................................................................. 4.68
Adjust HV AD Screen................................................................................. 4.71
Adjust Battery AD Screen........................................................................... 4.74
Paddle Contact A/D Screen........................................................................ 4.76
Check Hardware Screen....................................................................................... 4.77
Check Key Screen...................................................................................... 4.77
Check LED Screen..................................................................................... 4.79
Check LCD Screen..................................................................................... 4.80
Check Buzzer Screen................................................................................. 4.80
Check Voice Screen................................................................................... 4.81
Check Recorder Screen............................................................................. 4.83
Check ECG Frequency Screen.................................................................. 4.83
Check NIBP Screen.................................................................................... 4.84
Check 12 Lead Screen............................................................................... 4.91
Examination Screen................................................................................... 4.92
Check Time Constant Screen..................................................................... 4.92
Check MP Screen....................................................................................... 4.93
Operation Time Screen......................................................................................... 4.93
Version Up Screen................................................................................................ 4.94
Debug Mode Screen............................................................................................. 4.95
Check String Screen.................................................................................. 4.95
AD Viewer Screen................................................................................................. 4.96
Saving the System Maintenance Screens as Bitmap Files............................................. 4.97
Maintenance Check Sheet.............................................................................................. 4.98
Section 5 Replaceable Parts List........................................................... 5.1

GENERAL HANDLING PRECAUTIONS
This device is intended for use only by qualified medical personnel. Use only Nihon Kohden
approved products with this device. Use of non-approved products or in a non-approved
manner may affect the performance specifications of the device. This includes, but is not
limited to, batteries, recording paper, pens, extension cables, electrode leads, input boxes and
AC power.
Please read these precautions thoroughly before attempting to operate the instrument.
1. To safely and effectively use the instrument, its operation must be fully understood.
2. When installing or storing the instrument, take the following precautions:

(1) Avoid moisture or contact with water, extreme atmospheric pressure, excessive humidity and temperatures,
poorly ventilated areas, and dust, saline or sulphuric air.
(2) Place the instrument on an even, level floor. Avoid vibration and mechanical shock, even during transport.
(3) Avoid placing in an area where chemicals are stored or where there is danger of gas leakage.
(4) The power line source to be applied to the instrument must correspond in frequency and voltage to product
specifications, and have sufficient current capacity.
(5) Choose a room where a proper grounding facility is available.
3. Before Operation
(1) Check that the instrument is in perfect operating order.
(2) Check that the instrument is grounded properly.
(3) Check that all cords are connected properly.
(4) Pay extra attention when the instrument is in combination with other instruments to avoid misdiagnosis or other
problems.
(5) All circuitry used for direct patient connection must be doubly checked.
(6) Check that battery level is acceptable and battery condition is good when using battery-operated models.
4. During Operation
(1) Both the instrument and the patient must receive continual, careful attention.
(2) Turn power off or remove electrodes and/or transducers when necessary to assure the patient’s safety.
(3) Avoid direct contact between the instrument housing and the patient.
5. To Shutdown After Use

(1) Turn power off with all controls returned to their original positions.
(2) Remove the cords gently; do not use force to remove them.
(3) Clean the instrument together with all accessories for their next use.
6. The instrument must receive expert, professional attention for maintenance and repairs. When the instrument is
not functioning properly, it should be clearly marked to avoid operation while it is out of order.
7. The instrument must not be altered or modified in any way.
8. Maintenance and Inspection

(1) The instrument and specified parts must undergo regular maintenance inspection at the interval which is specified
after the GENERAL HANDLING PRECAUTIONS section.
(2) If stored for extended periods without being used, make sure prior to operation that the instrument is in perfect
operating condition.
Service Manual TEC-8300 i

(3) Technical information such as parts list, descriptions, calibration instructions or other information is available for
qualified user technical personnel upon request from your Nihon Kohden representative.
9. When the instrument is used with an electrosurgical instrument, pay careful attention to the application and/or
location of electrodes and/or transducers to avoid possible burn to the patient.
WARRANTY POLICY
Nihon Kohden Corporation (NKC) shall warrant its products against all defects in materials and workmanship for one year
from the date of delivery. However, consumable materials such as recording paper, ink, stylus and battery are excluded
from the warranty.
NKC or its authorized agents will repair or replace any products which prove to be defective during the warranty period,
provided these products are used as prescribed by the operating instructions given in the operator’s and service manuals.
No other party is authorized to make any warranty or assume liability for NKC’s products. NKC will not recognize any
other warranty, either implied or in writing. In addition, service, technical modification or any other product change
performed by someone other than NKC or its authorized agents without prior consent of NKC may be cause for voiding
this warranty.
Defective products or parts must be returned to NKC or its authorized agents, along with an explanation of the failure.
Shipping costs must be pre-paid.
This warranty does not apply to products that have been modified, disassembled, reinstalled or repaired without Nihon
Kohden approval or which have been subjected to neglect or accident, damage due to accident, fire, lightning, vandalism,
water or other casualty, improper installation or application, or on which the original identification marks have been
removed.
In the USA and Canada other warranty policies may apply.
CAUTION
United States law restricts this product to sale by or on the order of a physician.
ii Service Manual TEC-8300

EMC RELATED CAUTION
This equipment and/or system complies with IEC 60601-1-2 International Standard for electromagnetic
compatibility for medical electrical equipment and/or system. However, an electromagnetic environment that
exceeds the limits or levels stipulated in IEC 60601-1-2, can cause harmful interference to the equipment
and/or system or cause the equipment and/or system to fail to perform its intended function or degrade
its intended performance. Therefore, during the operation of the equipment and/or system, if there is any
undesired deviation from its intended operational performance, you must avoid, identify and resolve the
adverse electromagnetic effect before continuing to use the equipment and/or system.
The following describes some common interference sources and remedial actions:
1. Strong electromagnetic interference from a nearby emitter source such as an authorized radio station
or cellular phone:
Install the equipment and/or system at another location. Keep the emitter source such as cellular phone
away from the equipment and/or system, or turn off the cellular phone.
2. Radio-frequency interference from other equipment through the AC power supply of the equipment
and/or system:
Identify the cause of this interference and if possible remove this interference source. If this is not
possible, use a different power supply.
3. Effect of direct or indirect electrostatic discharge:

Make sure all users and patients in contact with the equipment and/or system are free from direct or
indirect electrostatic energy before using it. A humid room can help lessen this problem.
4. Electromagnetic interference with any radio wave receiver such as radio or television:
If the equipment and/or system interferes with any radio wave receiver, locate the equipment and/or
system as far as possible from the radio wave receiver.
5. Interference of lightning:
When lightning occurs near the location where the equipment and/or system is installed, excessive
voltage may be generated in the equipment and/or system. In such a case, disconnect the AC power
cord from the equipment and/or system and operate the equipment and/or system by battery power, or
use an uninterruptible power supply.
6. Use with other equipment:

When the equipment and/or system is adjacent to or stacked with other equipment, the equipment
and/ or system may affect the other equipment. Before use, check that the equipment and/or system
operates normally with the other equipment.
7. Use of unspecified accessory, transducer and/or cable:

When an unspecified accessory, transducer and/or cable is connected to this equipment and/or system,
it may cause increased electromagnetic emission or decreased electromagnetic immunity. The specified
configuration of this equipment and/or system complies with the electromagnetic requirements with the
specified configuration. Only use this equipment and/or system with the specified configuration.
Service Manual TEC-8300 iii

Caution - continued
8. Use of unspecified configuration:

When the equipment and/or system is used with the unspecified system configuration different than
the configuration of EMC testing, it may cause increased electromagnetic emission or decreased
electromagnetic immunity. Only use this equipment and/or system with the specified configuration.
9. Measurement with excessive sensitivity:

The equipment and/or system is designed to measure bioelectrical signals with a specified sensitivity. If
the equipment and/or system is used with excessive sensitivity, artifact may appear by electromagnetic
interference and this may cause mis-diagnosis. When unexpected artifact appears, inspect the
surrounding electromagnetic conditions and remove this artifact source.
If the above suggested remedial actions do not solve the problem, consult your Nihon Kohden
representative for additional suggestions.
For EMC compliance, refer to “Specifications - Electromagnetic Compatibility” in the General section.
The CE mark is a protected conformity mark of the European Community. Products with the CE mark comply
with the requirements of the Medical Device Directive 93/42/EEC.
NOTE about Waste Electrical and Electronic Equipment (WEEE) Directive 2002/96/EC
For the member states of the European Union only:
The purpose of WEEE directive 2002/96/EC is, as a first priority, the prevention of waste electrical and
electronic equipment (WEEE), and in addition, the reuse, recycling and other forms of recovery of such
wastes so as to reduce the disposal of waste.
Contact your Nihon Kohden representative for disposal.
iv Service Manual TEC-8300

Conventions Used in this Manual and Instrument
Warnings, Cautions and Notes

Warnings, cautions and notes are used in this manual to alert or signal the reader to specific information.
WARNING
A warning alerts the user to possible injury or death associated with the use or misuse of the instrument.
CAUTION
A caution alerts the user to possible injury or problems with the instrument associated with its use or
misuse such as instrument malfunction, instrument failure, damage to the instrument, or damage to other
property.
NOTE
A note provides specific information, in the form of recommendations, prerequirements, alternative methods or
supplemental information.
Service Manual TEC-8300 v

Related Documentation
The TEC-8321K, TEC-8322K, TEC-8332K, TEC-8342K and TEC-8352K defibrillators come with the following manuals.
Operator’s Manual, Part I General & Defibrillation

Describes general information (including safety information, installation procedure, basic checks and settings,
troubleshooting and specifications), defibrillation and pacing.
Operator’s Manual, Part II Parameter Monitoring

Describes parameter monitoring.
Administrator’s Guide
Describes settings on the SYSTEM SETUP screen.
Service Manual
Describes information on servicing the defibrillator. Only qualified service personnel can service the defibrillator.
vi Service Manual TEC-8300

1
Section 1 General
Introduction........................................................................................................................................................... 1.3
Models and Functions................................................................................................................................ 1.3
Parameters................................................................................................................................................. 1.3
General Information on Servicing......................................................................................................................... 1.4
Service Policy, Service Parts and Patient Safety Checks..................................................................................... 1.6
Service Policy............................................................................................................................................. 1.6
Service Parts.............................................................................................................................................. 1.6
Patient Safety Checks................................................................................................................................ 1.7
Maintenance Equipments and Tools........................................................................................................... 1.8
Specifications....................................................................................................................................................... 1.9
Defibrillator................................................................................................................................................. 1.9
Analysis Accuracy.................................................................................................................................... 1.12
Monitor..................................................................................................................................................... 1.13
Alarm Delay Time..................................................................................................................................... 1.13
Lead ECG................................................................................................................................................. 1.13
Paddle ECG............................................................................................................................................. 1.13
External ECG........................................................................................................................................... 1.13
Recorder................................................................................................................................................... 1.14
Noninvasive Pacing (TEC-8332/TEC-8352 Only)..................................................................................... 1.14
External Paddle (ND-831V)...................................................................................................................... 1.14
ECG.......................................................................................................................................................... 1.14
SpO2 ........................................................................................................................................................ 1.14
CO2 .......................................................................................................................................................... 1.14
NIBP (TEC-8342/TEC-8352 only)............................................................................................................ 1.14
Invasive Blood Pressure........................................................................................................................... 1.15
Temperature............................................................................................................................................. 1.15
Alarm........................................................................................................................................................ 1.15
Battery...................................................................................................................................................... 1.16
AC Power Requirements.......................................................................................................................... 1.16
Clock Accuracy......................................................................................................................................... 1.16
Environment............................................................................................................................................. 1.16
Dimensions and Weight............................................................................................................................ 1.16
Safety....................................................................................................................................................... 1.17
Environment Conditions........................................................................................................................... 1.17
Electromagnetic Compatibility.................................................................................................................. 1.18
Electromagnetic Emissions...................................................................................................................... 1.18
Electromagnetic Immunity........................................................................................................................ 1.19
Recommended Separation Distances between Portable and Mobile RF Communications Equipment... 1.22
System Configuration for EMC Test......................................................................................................... 1.23
Panel Description............................................................................................................................................... 1.24
Front Panel............................................................................................................................................... 1.24
Right Side Panel....................................................................................................................................... 1.25
Left Side Panel......................................................................................................................................... 1.26
Service Manual TEC-8300 1.1

Rear Panel............................................................................................................................................... 1.27
ND-831V External Paddles (Option)........................................................................................................ 1.28
ND-860V Series Internal Paddles (Option).............................................................................................. 1.29
ND-890V Series Internal Paddles (Option).............................................................................................. 1.29
Composition........................................................................................................................................................ 1.30
Standard Components............................................................................................................................. 1.30
TEC-8321....................................................................................................................................... 1.30
TEC-8322....................................................................................................................................... 1.31
TEC-8332....................................................................................................................................... 1.32
TEC-8342....................................................................................................................................... 1.33
TEC-8352....................................................................................................................................... 1.34
Options..................................................................................................................................................... 1.35
Board and Unit Location..................................................................................................................................... 1.37
1.2 Service Manual TEC-8300

1. GENERAL
1
Introduction
This service manual provides useful information to qualified service personnel

to understand, troubleshoot, service, maintain and repair this TEC-8300 series
defibrillator.
The information in the operator’s manual is primarily for the user. However, it
is important for service personnel to thoroughly read the operator’s manual and
service manual before starting to troubleshoot, service, maintain or repair this
defibrillator. This is because service personnel need to understand the operation
of the defibrillator in order to effectively use the information in the service
manual.
For simplicity, the suffix C/K for the defibrillator and its options are omitted in
this manual. There is no difference in operation among models with different
suffixes unless otherwise specified.
Models and Functions
Functions TEC-8321 TEC-8322 TEC-8332 TEC-8342 TEC-8352

Defibrillation
External paddles Option Option Option Option Option

Internal paddles Option Option Option Option Option
Disposable pads Option Option Option Option Option
AED Standard Standard Standard Standard Standard
Pacing — — Standard — Standard
Playing voice Standard Standard Standard Standard Standard
Sound recording Standard Standard Standard Standard Standard
12 lead ECG Option Option Option Option Option
ECG input Option Option Option Option Option
ECG output Option Option Option Option Option
SD card Option Option Option Option Option
Battery pack Option Option Option Option Option
AC/DC module Option Option Option Option Option
Bluetooth® module Option Option Option Option Option
Parameters
Functions TEC-8321 TEC-8322 TEC-8332 TEC-8342 TEC-8352

ECG monitoring Available Available Available Available Available
SpO2 monitoring Available Available Available Available Available
Temperature monitoring — Available Available Available Available
NIBP measurement — — — Available Available
Multi-parameter (1)* monitoring Available Available Available Available Available
Multi-parameter (2)* monitoring — Available Available Available Available
* CO2, invasive blood pressure or temperature monitoring is available.

1. GENERAL
General Information on Servicing
Note the following information when servicing the defibrillator.
CAUTION
Safety
• There is the possibility that the outside surface of the defibrillator,
such as the operation keys, could be contaminated by contagious
germs, so disinfect and clean the defibrillator before servicing it.
When servicing the defibrillator, wear rubber gloves to protect
yourself from infection.
• There is the possibility that when the lithium battery is broken,
a solvent inside the lithium battery could flow out or a toxic
substance inside it could come out. If the solvent or toxic
substance touches your skin or gets into your eye or mouth,
immediately wash it with a lot of water and see a physician.
Liquid ingress
• The defibrillator is not waterproof, so do not install the defibrillator
where water or liquid can get into or fall on the defibrillator. If
liquid accidentally gets into the defibrillator or the defibrillator
accidentally drops into liquid, disassemble the defibrillator, clean
it with clean water and dry it completely. After reassembling, verify
that there is nothing wrong with the patient safety checks and
function/performance checks. If there is something wrong with the
defibrillator, contact your Nihon Kohden representative to repair.
Environmental safeguards
• Depending on the local laws in your community, it may be illegal to
dispose of the lithium battery in the regular waste collection. Check
with your local officials for proper disposal procedures.
Disinfection and cleaning

• To disinfect the outside surface of the defibrillator, wipe it with a
non-abrasive cloth moistened with neutral detergent.

1. GENERAL
1
Transport
• Use the specified shipment container and packing material to
transport the defibrillator. If necessary, double pack the defibrillator.
Also, put the defibrillator into the shipment container after packing
so that the buffer material does not get into the inside of the
defibrillator.
• When transporting a board or unit of the defibrillator, be sure to use
a conductive bag. Never use an aluminum bag when transporting
a board or unit which a lithium battery is mounted. Also, never use
a styrene foam or plastic bag which generates static electricity to
wrap the board or unit of the defibrillator.
Handling the defibrillator

• Because the outside surface of the defibrillator is made of resin,
the outside surface of the defibrillator is easily damaged. So when
handling the defibrillator, remove clutter from around the system
and be careful to not damage the defibrillator or get it dirty.
• Because most of the boards in the defibrillator are multilayer boards
with surface mounted electrical devices (SMD), when removing and
soldering the electrical devices, a special tool is required. To avoid
damaging other electrical components, do not remove and solder
SMD components yourself.
Measuring and test equipment

• Maintain the accuracy of the measuring and test equipment by
checking and calibrating it according to the check and calibration
procedures.
Preventing infection
• Follow the local laws or regulations to prevent infection.

1. GENERAL
Service Policy, Service Parts and Patient Safety Checks
Service Policy
Our technical service policy for this defibrillator is to replace the faulty unit,
board or part or damaged mechanical part with a new one. Do not perform
electrical device or component level repair of the multilayer board or unit. We do
not support component level repair outside the factory for the following reasons:
• Most of the boards are multilayer boards with surface mounted electrical
devices, so the mounting density of the board is too high.
• A special tool or high degree of repair skill is required to repair the multilayer
boards with surface mounted electrical devices.
Only disassemble the defibrillator or replace a board or unit in an environment

where the defibrillator is protected against static electricity.
As background knowledge for repair, note the following:

• You can reduce the repair time by considering the problem before starting
repair.
• You can clarify the source of most of the troubles using the information from
the troubleshooting tables. Refer to “Troubleshooting” of this manual.
Service Parts
Refer to “Replaceable Parts List” of this manual for the service parts for
technical service that we provide.
NOTE
When ordering parts or accessories from your Nihon Kohden
representative, please quote the code number and part name which is
listed in this service manual, and the name or model of the unit in which
the required part is located. This will help us to promptly attend to your
needs. Always use parts and accessories recommended or supplied by
Nihon Kohden Corporation to assure maximum performance from your
defibrillator.

1. GENERAL
Patient Safety Checks 1

Periodic maintenance procedures and diagnostic check procedures are provided
in this manual to ensure that the defibrillator is operating in accordance with its
design and production specifications. To verify that the defibrillator is working
in a safe manner with regard to patient safety, patient safety checks should
be performed on the defibrillator before it is first installed, periodically after
installation, and after any repair is made on the defibrillator.
For patient safety checks, perform the following checks as described in the
IEC60601-1 “Medical electrical equipment - Part 1: General requirements for
safety”:
• Protective earth resistance check
• Earth leakage current check
• Enclosure leakage current check
• patient auxiliary current check
• Withstanding voltage check
NOTE
When using a delivery checker to input ECG to the defibrillator, the ECG
polarity depends on the delivery checker model and connection of the
pads/paddles. For details on a delivery checker, refer to the manual of the
delivery checker.

1. GENERAL
Maintenance Equipments and Tools
Item to be Checked Equipment and Tool

Appearance Power cord Earth resistance meter
Defibrillator Recorder • Ruler
• Stopwatch
• Recording paper
Defibrillation • Defibrillation • AX-103V defibrillation analyzer (Nihon Kohden)
and pacing • Synchronized cardioversion • Oscilloscope
• AED • Stopwatch
• Pacing (TEC-8332/8352 only) • JC-865V pad adapter
• JC-906P ECG connection cord
• BR-903P electrode lead
Monitoring ECG • AX-400G vital sign simulator (Nihon Kohden)
• BJ-900P ECG patient cable
IBP • AX-400G vital sign simulator (Nihon Kohden)
• H-0753 BSS cable for AX-400G vital sign simulator
CO2 (defibrillator) • AX-400G vital sign simulator (Nihon Kohden)
CO2 (CO2 sensor kit) • CO2 5% sensitivity gas A-4
• PR-150 flow regulator
• CO2 sensor kit
• Airway adapter
SpO2 • AX-400G vital sign simulator (Nihon Kohden)
• JL-900P SpO2 connection cord
• H-0750 SpO2 connection cable
NIBP (TEC-8342/8352 only) • YP-963T NIBP cuff, adult, latex free
• YN-901P air hose (adult, 3.5 m)
Temperature • AX-400G vital sign simulator (Nihon Kohden)
• HR10 connector compatible connection cable for
AX-800P vital sign simulator (code no.: 095567C)
12 lead ECG unit • AX-400G vital sign simulator (Nihon Kohden)
• BJ-900P ECG patient cable
Safety Leakage current LCC-1101 leakage current checker (Nihon Kohden)
NOTE
When using a delivery checker to input ECG to the defibrillator, the ECG
polarity depends on the delivery checker model and connection of the
pads/paddles. For details on a delivery checker, refer to the manual of the
delivery checker.

1. GENERAL
1
Specifications
Defibrillator
Output energy (across 50 Ω): 2, 3, 5, 7, 10, 15, 20, 30, 50, 70, 100, 150, 200 and 270 J
Energy accuracy: 2 J: ±0.5 J, 3 J: ±1 J, 5 to 15 J: ±2 J, 20 to 270 J: ±10%
Output waveform: Biphasic, truncated exponential constant power
Charging time:
Manual mode:
• From when the CHARGE/AED button is pressed to when there are charged sounds
When powered by AC 100 V to 240 V: to 270 J, maximum 5 s
to 200 J, maximum 4 s
When powered by a fully charged new battery at 20°C ambient temperature:
When powered by 90% of the rated mains voltage: to 270 J, maximum 7 s
After 15 discharges at 270 J with a fully charged new battery at 20°C ambient temperature:
• From when the defibrillator power is on to when there are charged sounds
When powered by 90% of the rated mains voltage: to 270 J, maximum 14 s
AED mode:
• From when the CHARGE/AED button is pressed to when there are charged sounds
When powered by AC 100 V to 240 V: to 270 J, maximum 8 to 15 s
When powered by a fully charged new battery at 20°C ambient temperature:
to 270 J, maximum 8 to 15 s
When powered by 90% of the rated mains voltage: to 270 J, maximum 8 to 15 s
• From when the defibrillator power is on to when there are charged sounds
When powered by 90% of the rated mains voltage: to 270 J, maximum 16 to 23 s
Charging display: Displays the charged energy value on the screen
Synchronized discharge: Available
From the peak of R wave to the peak of discharge: within 60 ms
Maximum skin-disposable pad contact impedance for energy charging: 350 Ω
Maximum continuous charge/discharge cycles at 270 J (across 50 Ω)
20 cycles: 3 cycles per minute with 1 minute cool down period after every 1
minute charge/discharge period
15 cycles: 3 cycles per minute with no cool down period

1. GENERAL
Discharged waveform
Delivered energy: 270 J
Load First phase Duration between Second phase

resistance (Ω) Ipk1 (A) D1 (ms) It (A) the 2 phases (ms) Ipk2 (A) D2 (ms) D3 (ms)
25 67.30 3.85 26.80 ≤ 0.5 15.50 3.62 < 6.5
50 41.10 6.35 15.50 ≤ 0.5 12.70 3.62 < 6.5
75 29.50 8.86 11.00 ≤ 0.5 11.00 3.62 < 6.5
100 22.90 11.40 8.50 ≤ 0.5 9.81 3.62 < 6.5
125 18.80 13.90 6.94 ≤ 0.5 8.96 3.62 < 6.5
150 15.90 16.40 5.86 ≤ 0.5 8.29 3.62 < 6.5
175 13.80 18.90 5.08 ≤ 0.5 7.76 3.62 < 6.5

25 58.10 3.85 22.6 ≤ 0.5 13.00 3.62 < 6.5
50 35.40 6.36 13.3 ≤ 0.5 10.90 3.62 < 6.5
75 25.40 8.86 9.45 ≤ 0.5 9.45 3.62 < 6.5
100 19.80 11.40 7.32 ≤ 0.5 8.45 3.62 < 6.5
125 16.20 13.90 5.97 ≤ 0.5 7.71 3.62 < 6.5
150 13.70 16.40 5.05 ≤ 0.5 7.14 3.62 < 6.5
175 11.90 18.90 4.37 ≤ 0.5 6.67 3.62 < 6.5

25 50.4 3.85 19.6 ≤ 0.5 11.3 3.62 < 6.5
50 30.8 6.36 11.5 ≤ 0.5 9.42 3.62 < 6.5
75 22.1 8.86 8.19 ≤ 0.5 8.19 3.62 < 6.5
100 17.2 11.40 6.34 ≤ 0.5 7.32 3.62 < 6.5
125 14.1 13.90 5.18 ≤ 0.5 6.69 3.62 < 6.5
150 11.9 16.40 4.37 ≤ 0.5 6.18 3.62 < 6.5
175 10.3 18.90 3.79 ≤ 0.5 5.78 3.62 < 6.5

1. GENERAL
Delivered energy: 100 J 1

25 41.3 3.86 16.0 ≤ 0.5 9.21 3.62 < 6.5
50 25.1 6.36 9.42 ≤ 0.5 7.69 3.62 < 6.5
75 18.0 8.87 6.68 ≤ 0.5 6.68 3.62 < 6.5
100 14.0 11.4 5.18 ≤ 0.5 5.98 3.62 < 6.5
125 11.5 13.9 4.22 ≤ 0.5 5.45 3.62 < 6.5
150 9.75 16.4 3.57 ≤ 0.5 5.05 3.62 < 6.5
175 8.45 18.9 3.09 ≤ 0.5 4.72 3.62 < 6.5

25 34.6 3.86 13.4 ≤ 0.5 7.71 3.62 < 6.5
50 21.1 6.36 7.88 ≤ 0.5 6.44 3.62 < 6.5
75 15.2 8.87 5.59 ≤ 0.5 5.59 3.62 < 6.5
100 11.8 11.4 4.33 ≤ 0.5 5.00 3.62 < 6.5
125 9.66 13.9 3.54 ≤ 0.5 4.57 3.62 < 6.5
150 8.18 16.4 2.99 ≤ 0.5 4.22 3.62 < 6.5
175 7.09 18.9 2.58 ≤ 0.5 3.95 3.62 < 6.5

25 29.4 3.86 11.3 ≤ 0.5 6.52 3.62 < 6.5
50 17.9 6.37 6.67 ≤ 0.5 5.45 3.62 < 6.5
75 12.9 8.88 4.73 ≤ 0.5 4.73 3.62 < 6.5
100 10.0 11.4 3.66 ≤ 0.5 4.23 3.62 < 6.5
125 8.20 13.9 2.99 ≤ 0.5 3.86 3.62 < 6.5
150 6.95 16.4 2.53 ≤ 0.5 3.57 3.62 < 6.5
175 6.02 18.9 2.19 ≤ 0.5 3.34 3.62 < 6.5

1. GENERAL
Output Waveforms: 200 J/25, 50, 75, 100, 125, 150, 175 Ω
Analysis Accuracy
We evaluated the rhythm recognition detector of the TEC-8300 series defibrillator using the official electrocardiogram
database provided by AHA (American Heart Association) and MIT (Massachusetts Institute of Technology) and an
electrocardiogram database of over 3000 electrocardiograms from hospitals in Japan. According to our own evaluation, the
rhythm recognition detector of the TEC-8300 series defibrillator meets the equivalent of IEC 60601-2-4: 2002 6.8.3 aa) 3) a).
Shockable Rhythm VF: Sensitivity: ≥ 90%
Shockable Rhythm VT: Sensitivity: ≥ 75%
All other Non-Shockable Rhythm: Specificity: ≥ 95%
The TEC-8300 series defibrillator continues to analyze the heart rhythm after it determines that a defibrillation shock
is required. When the heart rhythm changes and the TEC-8300 series defibrillator determines that a defibrillation shock
should no longer be delivered, the Shock Button stops flashing, disabling delivery of a defibrillation shock.
The above analysis accuracy is ensured when the ECG contains a pacemaker pulse with amplitude less than 2 mV and
width less than 1.3 ms.

1. GENERAL
Monitor 1
Effective display area: 170.4 (W) × 127.8 (H) mm
Sweep length: 136.2 mm
Sweep speed: 25 mm/s, 50 mm/s
Sensitivity: 10 mm/1 mV ±10% (sensitivity ×1)
Amplitude limit: 122.7 mm
Alarm Delay Time

Heart Rate HR change from 80 to 120 bpm: ≤10 seconds (upper limit: 100 bpm)
HR change from 80 to 40 bpm: ≤10 seconds (lower limit: 60 bpm)
Pulse rate Response time of heart rate meter to change in heart rate:
PR change from 80 to 120 bpm: ≤15 seconds (upper limit: 100 bpm)
PR change from 80 to 40 bpm: ≤20 seconds (lower limit: 60 bpm)
ST: Approx. 1 second after measurement value reaches alarm threshold
(averaged 15-second data)
VPC: Approx. 1 second after measurement value reaches alarm threshold
Respiration rate: Approx. 1 second after measurement value reaches alarm threshold
(with 4 respiration intervals)
NIBP: Approx. 1 second after measurement value becomes stable
IBP: IBP change from 100 to 60 mmHg ≤ 10 seconds
(at pulse rate 80 bpm, SYS lower limit: 80 mmHg)
SpO2: Approx. 1 second after measurement value reaches alarm threshold
Temperature: Approx. 1 second after measurement value reaches alarm threshold
CO2 (Mainstream and sidestream method):
Approx. 1 second after measurement value reaches alarm threshold
(when the next respiration is detected)
Lead ECG
Input signal: PADDLE, I, II, III, aVR, aVL, aVF, V1, V2, V3, V4, V5, V6, AUX
Sensitivity: 10 mm/mV ±5% (sensitivity ×1)
Frequency response (in Monitor mode): DIAG mode: 0.05 to 150 Hz
MONITOR mode: 0.5 to 40 Hz
MAXIMUM mode: 1 to 18 Hz
Input impedance: Input impedance: ≥ 5 MΩ
CMRR: ≥ 100 dB (when the AC hum filter is set to ON)
AC hum filter: ≤ 20 dB attenuation (at 50 or 60 Hz)
Paddle ECG
Frequency response: 0.5 to 20 Hz
Input impedance: Input impedance: ≥ 100 kΩ
AC hum filter: attenuation ratio ≥ 20 dB (at 50 or 60 Hz)
External ECG
Input impedance: Input impedance: 100 kΩ ±10%

1. GENERAL
Recorder
Sensitivity: 10 mm/mV ±10%
Frequency response: 0.05 to 150 Hz
Paper speed: Real time/delayed ECG waveform recording: 50, 25 mm/s ±10%
Types of recording:
Automatic recording: Record on charging after discharge, alarm recording, periodic recording
Noninvasive Pacing (TEC-8332/TEC-8352 Only)

Pacing rate: 30 to 180 pulse/min ±10% in 10 pulse/min steps
Output current: 8 to 200 mA in 1 mA steps (accuracy of ± 2 mA or ±10%, whichever greater, at
250 Ω)
Pacing modes: Fixed and Demand
Maximum load resistance: Outputs 200 mA across 350 Ω
Pulse width: 40 ms±10%
Pacing pulse waveform: Modified trapezoidal
External Paddle (ND-831V)

Paddle electrode size: For adults: 70 ±3 × 106 ±3 (mm)
For children: 45 ±3 × 53 ±3 (mm)
Paddle cord length: 2.0 m or more
ECG
Pacing pulse rejection: ON, OFF
Pacing pulse rejection capability: Square-wave pulse of ±2 mV to ±0.7 V, 0.1 ms to 2 ms
Heart rate counting range: Defibrillation or monitoring mode: 15 to 300 bpm
Pacing mode: 15 to 220 bpm
SpO2
Display range: 0 to 100%SpO2
Measuring accuracy (rms): 80%SpO2 ≤ %SpO2 ≤ 100%SpO2: ±2%SpO2
70%SpO2 ≤ %SpO2 < 80%SpO2: ±3%SpO2
Less than 70%SpO2 is not specified
Accuracy at surrounding temperature: 18 to 40°C (64.4 to 104°F)
Recovery time after defibrillation: within 3 s
CO2
CO2 measuring range: 0 to 99 mmHg (0 to 133 hPa)
Measurement accuracy: ±4 hPa (0 ≤ CO2 ≤ 13.3 hPa) (±3 mmHg (0 ≤ CO2 ≤ 10 mmHg))
±5.3 hPa (13.3 < CO2 ≤ 53.3 hPa) (±4 mmHg (10 < CO2 ≤ 40 mmHg))
±10% reading (53.3 < CO2 ≤ 133 hPa (40 < CO2 ≤ 99 mmHg))
(At 1 atmospheric pressure, air inspiration, no condensation)
Respiration rate counting range: 3 to 150 counts/min ±10%
Recovery time after defibrillation: within 3 s
NIBP (TEC-8342/TEC-8352 only)

Display items: Systolic (SYS), diastolic (DIA), mean (MAP), cuff pressure during NIBP
measurement
Cuff pressure display range: 0 to 300 mmHg ±3 mmHg

1. GENERAL
Safety 1
Maximum pressurization value cuff inflation limiter:
Adult/Child: 300 to 330 mmHg
Cuff inflation time limiter: Adult/Child: ≤ 180 s
Power discontinuity: Deflate immediately after power down
Measurement mode: Manual, STAT, Periodic
Alarm
Upper limit range: 15 to 260 mmHg in 5 mmHg steps, OFF
Lower limit range: OFF, 10 to 255 mmHg in 5 mmHg steps
Invasive Blood Pressure

Measuring range: –50 to +300 mmHg
Internal noise: within ±1 mmHg
Auto zero balancing range: ±200 mmHg
Frequency characteristics: DC to 12 ±3 Hz (–3 dB)
Temperature zero drift: ±0.1 mmHg/1°C
Discontinuity detection: detects transducer cable discontinuity
Temperature
Measuring range: 0 to 45°C (32 to 113°F)
Measuring accuracy: ±0.2°C (0°C ≤ Temperature < 25°C)
±0.1°C (25°C ≤ Temperature ≤ 45°C)
Internal noise: ≤ 0.014°C (at 37°C)
Temperature drift: within ±0.005°C/°C
Discontinuity detection: detects sensor cable discontinuity
Alarm
Alarm levels:
Crisis: Patient is in critical condition and the patient’s life may be at risk. Immediate
action must be taken.
Warning: Patient is in critical condition. Prompt action should be taken.
Advisory: Setting or condition is not appropriate for accurate monitoring.
Alarm indicator:
Crisis: red blinking: approx. 1.6 Hz (approx. 640 ms), duty 50%
Warning: yellow blinking: approx. 0.8 Hz (approx. 1280 ms), duty 50%
Advisory: cyan lighting
Alarm sound:
Crisis: Complies with IEC 60601-1-8
Warning: Complies with IEC 60601-1-8
Advisory: Complies with IEC 60601-1-8
Alarm silence: Available when there is an alarm. Silences the alarm for 2 minutes.
Alarm suspend: Available when no alarm occurs. Suspends all alarms for 2 minutes.
Alarm volume priority: Crisis ≥ Warning ≥ Advisory
Volume range: 45 to 85 dB (A) (Requirement of IEC 60601-2-49: 2001) (at 1 m in front of
defibrillator)

1. GENERAL
Battery
Number of battery slots: 2
Type: Lithium ion battery
Nominal voltage: 14.4 V
Rated capacity: 6300 mAh (90.7 wh)
Capacity with fully charged new battery at 20°C ambient temperature:
• Minimum 200 discharges at 270 J
• Minimum 240 minutes continuous monitoring
• Minimum 180 minutes fixed mode pacing (180 pulse/min, 200 mA)
With the fully charged new battery at 0°C
• Minimum 150 discharges at 270 J
AC Power Requirements
Line voltage: 100 to 240 V
Line frequency: 50/60 Hz
Power input: Intermittent load: 250 VA or less
Continuous load: 150 VA or less
Clock Accuracy
At surrounding temperature 25°C (77°F): ±5.2 s/month
Environment
Operating temperature: 0 to 45°C (32 to 113°F)
Operating humidity: 30 to 95% (relative humidity, noncondensing)
Operating atmospheric pressure: 700 to 1060 hPa
Storage temperature: −20 to +70°C (−4 to +158°F)
Storage humidity: 10 to 95% (relative humidity)
Storage atmospheric pressure: 500 to 1060 hPa
Dimensions and Weight

Dimensions: 334 (W) × 326 (H) × 262 (D) mm ±30 mm
Weight:
TEC-8321/TEC-8322/TEC-8332:
6.8 kg ±0.8 kg (including one battery pack)
TEC-8342/TEC-8352: 7.0 kg ±0.8 kg (including one battery pack)

1. GENERAL
Safety 1
Safety standard: IEC 60601-1: 1988
IEC 60601-1 Amendment 1: 1991
IEC 60601-1 Amendment 2: 1995
IEC 60601-1-1: 2000
IEC 60601-1-8: 2006
IEC 60601-2-4: 2002
Type of protection against electrical shock:
Battery power: INTERNALLY POWERED EQUIPMENT
AC power: CLASS I EQUIPMENT
Degree of protection against electrical shock:
DEFIBRILLATION-PROOF TYPE BF APPLIED PART:
External paddles, disposable pads and NIBP cuff
DEFIBRILLATION-PROOF TYPE CF APPLIED PART:
Internal paddles (with switch), ECG connection cable, 12 lead ECG cable,
thermistor probe, IBP catheter, SpO2 connection cord and CO2 sensor kit
Degree of protection against harmful ingress of water:
When operating on battery power. Available options are AC-831V 12 lead ECG
unit and QI-832V Bluetooth® module: IP24
( • Protects against access to hazardous parts with a finger
• Protected against solid foreign objects of 12.5 mm diameter and greater
• Protected against splashing water)
Other than above: IP21
( • Protects against access to hazardous parts with a finger
• Protected against solid foreign objects of 12.5 mm diameter and greater
• Protected against vertically falling water drops)
Degree of safety of application in the presence of a FLAMMABLE ANAESTHETIC MIXTURE WITH AIR, OR WITH
OXYGEN OR NITROUS OXIDE: EQUIPMENT not suitable for use in the presence of FLAMMABLE
ANAESTHETIC MIXTURE WITH AIR, OR WITH OXYGEN OR NITROUS
OXIDE
Mode of operation:
Continuous operation with intermittent load: Operation in defibrillation mode
Continuous operation: All operation except above mentioned
Environment Conditions
Vibration: MIL-STD-810F 514.5 Category 4 (Truck Restrained Cargo)
MIL-STD-810F 514.5 Category 9 (Helicopter)

1. GENERAL
Electromagnetic Compatibility
Standard
IEC 60601-1-2: 2001
Medical electrical equipment - Part 1-2: General requirements for safety - Collateral standard: Electromagnetic
compatibility - Requirements and tests
IEC 60601-1-2 Amendment 1: 2004
IEC 60601-2-4: 2002

Medical electrical equipment - Part 2-4: Particular requirement for the safety of cardiac defibrillators
Electromagnetic Emissions
The TEC-8300’s essential performances in EMC standard satisfy the following criteria.
The TEC-8300 series is intended for use in the electromagnetic environment specified below. The customer or the user of
the TEC-8300 series should assure that it is used in such an environment.
Emissions test Compliance Electromagnetic environment – guidance

The TEC-8300 series uses RF energy only for its internal function.
RF emissions
Group 1 Therefore, its RF emissions are very low and are not likely to cause
CISPR 11
any interference in nearby electronic equipment.
RF emissions
Class B
CISPR 11
The TEC-8300 series is suitable for use in all establishments, including
Harmonic emissions
Class A domestic establishments and those directly connected to the public
IEC 61000-3-2
low-voltage power supply network that supplies buildings used for
Voltage fluctuations/ domestic purposes.
flicker emissions Complies
IEC 61000-3-3

1. GENERAL
Electromagnetic Immunity 1
The TEC-8300’s essential performances in EMC standard satisfy the following criteria.
The TEC-8300 series is intended for use in the electromagnetic environment specified below. The customer or the user of
the TEC-8300 series should assure that it is used in such an environment.
Electromagnetic environment –
Immunity test IEC 60601 test level Compliance level
guidance
Electrostatic ±6 kV contact ±6 kV contact Floors should be wood, concrete or ceramic
discharge (ESD) ±8 kV air ±8 kV air tile. If floors are covered with synthetic
IEC 61000-4-2 material, the relative humidity should be at
least 30%.
Electrical fast ±2 kV for power supply ±2 kV for power supply Mains power quality should be that
transient/burst lines lines of a typical commercial or hospital
IEC 61000-4-4 ±1 kV for input/output Not applicable environment.
lines When there is large noise on the AC power
line, supply the power from the battery
pack.
Surge ±1 kV differential mode ±1 kV differential mode Mains power quality should be that
IEC 61000-4-5 ±2 kV common mode ±2 kV common mode of a typical commercial or hospital
environment.
Voltage dips, short < 5% UT < 5% UT Mains power quality should be that
interruptions and (> 95 % dip in UT) for (> 95% dip in UT) for of a typical commercial or hospital
voltage variations on 0.5 cycles 0.5 cycles environment. If the user of the TEC-8300
power supply input lines series requires continued operation
IEC 61000-4-11 40% UT 40% UT during power mains interruptions, it is
(60% dip in UT) for (60 % dip in UT) for recommended that the TEC-8300 series
5 cycles 5 cycles be powered from an uninterruptible power
supply or a battery.
70% UT 70% UT
(30% dip in UT) for (30% dip in UT) for
25 cycles 25 cycles
Voltage dips, short < 5% UT < 5% UT Mains power quality should be that
interruptions and (> 95 % dip in UT) for (> 95 % dip in UT) for of a typical commercial or hospital
voltage variations on 5 seconds 5 seconds environment. If the user of the TEC-
power supply input lines 8300 series requires continued operation
IEC 61000-4-11 during power mains interruptions, it is
recommended that the TEC-8300 series
be powered from an uninterruptible power
supply or a battery.
Power frequency 3 A/m 3 A/m Power frequency magnetic fields should
(50/60 Hz) magnetic be at levels characteristic of a typical
field location in a typical commercial or hospital
IEC 61000-4-8 environment.
NOTE 1: UT is the AC mains voltage prior to application of the test level.
NOTE 2: Noise from the AC power line may generate noise which is superimposed on the ECG waveforms.

1. GENERAL
IEC 60601
Immunity test Compliance level Electromagnetic environment – guidance
test level
Portable and mobile RF communications
equipment should be used no closer to any part of
the TEC-8300 series, including cables, than the
recommended separation distance calculated from
the equation applicable to the frequency of the
transmitter.
Recommended separation distance

Conducted RF 3 Vrms 3 Vrms d = 1.2 P
IEC 61000-4-6 150 kHz to 80 MHz
outside ISM bands*1 where P is the maximum output power rating
of the transmitter in watts (W) according to the
transmitter manufacturer and d is the recommended
separation distance in meters (m).*2
Field strengths from fixed RF transmitters, as

determined by an electromagnetic site survey,*3
should be less than the compliance level in each
frequency range.*4
Interference may occur in the vicinity of equipment

marked with the following symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
NOTE 2: These guidelines might not apply in all situations. Electromagnetic propagation is affected by absorption and
reflection from structures, objects and people.
* The ISM (industrial, scientific and medical) bands between 150 kHz and 80 MHz are 6.765 MHz to 6.795 MHz;
1
13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz.
*2 The compliance levels in the ISM frequency bands between 150 kHz and 80 MHz and in the frequency range
80 MHz to 2.5 GHz are intended to decrease the likelihood that mobile/portable communications equipment could
cause interference if it is inadvertently brought into patient areas. For this reason, an additional factor of 10/3 is used
in calculating the recommended separation distance for transmitters in these frequency ranges.
*3 Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile
radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy.
To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be
considered. If the measured field strength in the location in which the TEC-8300 series is used exceeds the applicable
RF compliance level above, the TEC-8300 series should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as re-orienting or relocating the TEC-8300
series.
*4 Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.

1. GENERAL
IEC 60601 Compliance 1

Immunity test Electromagnetic environment – guidance
test level level
Portable and mobile RF communications
equipment should be used no closer to any part of
the TEC-8300 series, including cables, than the
recommended separation distance calculated from
the equation applicable to the frequency of the
transmitter.
Recommended separation distance

Radiated RF IEC 61000-4-3 3 V/m d = 1.2 P 80 to 800 MHz
IEC 61000-4-3 d = 2.3 P 800 MHz to 2.5 GHz
Requirement of Additional requirement of IEC 60601-2-4

IEC 60601-2-4:
Correct operation of RRD: Correct operation of RRD:

10 V/m 10 V/m d = 4.0 P 80 to 800 MHz
80 MHz to 2.5 GHz d = 7.7 P 800 MHz to 2.5 GHz
No inadvertent energy
delivery is allowed: No inadvertent energy delivery is allowed:
20 V/m 20 V/m d = 0.6 P 80 to 800 MHz
80 MHz to 2.5 GHz d = 1.2 P 800 MHz to 2.5 GHz
where P is the maximum output power rating

of the transmitter in watts (W) according to the
transmitter manufacturer and d is the recommended
separation distance in meters (m).*2
Field strengths from fixed RF transmitters, as

determined by an electromagnetic site survey,*3
should be less than the compliance level in each
frequency range.*4
Interference may occur in the vicinity of equipment

marked with the following symbol:
NOTE 1: At 80 MHz and 800 MHz, the higher frequency range applies.
* The ISM (industrial, scientific and medical) bands between 150 kHz and 80 MHz are 6.765 MHz to 6.795 MHz;
1
13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz.
*2 The compliance levels in the ISM frequency bands between 150 kHz and 80 MHz and in the frequency range
80 MHz to 2.5 GHz are intended to decrease the likelihood that mobile/portable communications equipment could
cause interference if it is inadvertently brought into patient areas. For this reason, an additional factor of 10/3 is used
in calculating the recommended separation distance for transmitters in these frequency ranges.
*3 Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land mobile
radios, amateur radio, AM and FM radio broadcast and TV broadcast cannot be predicted theoretically with accuracy.
To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site survey should be
considered. If the measured field strength in the location in which the TEC-8300 series is used exceeds the applicable
RF compliance level above, the TEC-8300 series should be observed to verify normal operation. If abnormal
performance is observed, additional measures may be necessary, such as re-orienting or relocating the TEC-8300
series.
*4 Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 3 V/m.
• RRD is the abbreviation of Rhythm Recognition Detector.

1. GENERAL
Recommended Separation Distances between Portable and Mobile RF Communications Equipment
The TEC-8300 series is intended for use in an electromagnetic environment in which radiated RF disturbances are
controlled. The customer or the user of the TEC-8300 series can help prevent electromagnetic interference by maintaining a
minimum distance between portable and mobile RF communications equipment (transmitters) and the TEC-8300 series as
recommended below, according to the maximum output power of the communications equipment.
Separation distance according to frequency of transmitter (m)

Rated maximum output 150 kHz to 80 MHz 150 kHz to 80 MHz
power of transmitter (W) outside ISM bands 80 MHz to 800 MHz 800 MHz to 2.5 GHz
in ISM bands
d = 1.2 P d = 2.3 P
d = 1.2 P d = 1.2 P
0.01 0.12 0.12 0.4 0.77
0.1 0.38 0.38 1.3 2.4
1 1.2 1.2 4.0 7.7
10 3.8 3.8 13 27
100 12 12 40 77
For transmitters rated at a maximum output power not listed above, the recommended separation distance d in meters
(m) can be determined using the equation applicable to the frequency of the transmitter, where P is the maximum output
power rating of the transmitter in watts (W) according to the transmitter manufacturer.
NOTE 1: At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
NOTE 2: The ISM (industrial, scientific and medical) bands between 150 kHz and 80 MHz are 6.765 MHz to
6.795 MHz; 13.553 MHz to 13.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to 40.70 MHz.
NOTE 3: An additional factor of 10/3 is used in calculating the recommended separation distance for transmitters in
the ISM frequency bands between 150 kHz and 80 MHz and in the frequency range 80 MHz to 2.5 GHz
to decrease the likelihood that mobile/portable communications equipment could cause interference if it is
inadvertently brought into patient areas.
The equations and values in the above table show the condition that the RRD (Rhythm Recognition Detector) regulated
in IEC 60601-2-4: 2002 does not receive electromagnetic interference.

1. GENERAL
System Configuration for EMC Test 1

We tested that the defibrillator complies with IEC 60601-1-1: 2001, Amendment 1: 2004 and IEC 60601-2-4: 2002 with
the following configuration. If other cables and equipments are used with the defibrillator, the defibrillator may not comply
with these standards.
Configuration at testing Cable length (m)

Defibrillator, TEC-8300 series —
Pad adapter, JC-865V 3.50
Patient cable, BJ-831V 3.30
12 lead electrode, BR-906V 0.6
CO2 sensor kit, TG-900P 2.99
SpO2 connection cord, JL-900P 2.50
Finger probe, TL-201T 1.60
AC/DC module, SC-831V —
Battery pack, SB-831V —
SD card, QM-001D —
PRESS connection cord, JP-900P 3.5
Monitoring kit, DX-300 2.1
Thermistor probe, 409J 3.4
Air hose for adult/child, YN-901P 3.5
Cuff for adult, YP-963T —
Connection cable, P-112D 1.5

1. GENERAL
Panel Description
Front Panel
22 1
2
21
20 4
19
5
18
27
6
17
7
26
23 24 25
10 9
11 12 13 14 15 16
Illustration above shows the example when the optional ND-831V external
paddles are used.
No. Name No. Name
1 Alarm indicator 18 Pacing rate up/down keys*
2 Status indicator 19 START/STOP key*
3 SYNC button 20 PULSE lamp*
4 Control dial 21 Handle
5 Child mode button 22 LCD display
6 CHARGE/AED button 23 AC power lamp
7 SHOCK button 24 Battery charging lamp
8 Paddle connector 25 Battery charging completion lamp
9 Record/stop key 26 Speaker
10 SILENCE ALARMS key 27 Microphone
11 to 16 Function keys 1 to 6 * TEC-8332/8352 defibrillators only.
17 Pacing output up/down keys*

1. GENERAL
Right Side Panel 1
2
1
paddles are used.
No. Name
1 SD card slot
2 AUXOUT socket (only when using the optional QI-831V AUXOUT unit)
3 Door release lever
4 Paper container

1. GENERAL
Left Side Panel
paddles are used.
No. Name
1 SpO2 socket
2 TEMP modular jack
3 MULTI socket
4 NIBP socket
5 ECG socket

1. GENERAL
Rear Panel 1
2
3
paddles are used.
No. Name
1 External paddle holder (option)
2 Battery slot A connector
3 AC/DC module/battery slot B connector

1. GENERAL
ND-831V External Paddles (Option)

1
No. Name
1 Shock buttons
2 Paddle contact lamp
3 Charge button

1. GENERAL
ND-860V Series Internal Paddles (Option) 1

2
1
No. Name
1 Paddle connector
2 Electrodes
3 Handles
ND-890V Series Internal Paddles (Option)

2
1
No. Name
1 Paddle connector
2 Electrodes
3 Handles
4 Shock button

1. GENERAL
Composition
Boards in a dotted rectangle cannot be ordered separately. To get that board,

order the board which includes the board in the a dotted rectangle.
Standard Components
TEC-8321
TEC-8321
Defibrillator
UR-0414
CONTROL
UR-04151 No PACER
ECG/PACER
UR-04161 No PACER SW
KEY/LED UR-0452
KEY/LED1
UR-0453
KEY/LED2
UR-0417
POWER
UR-0429 UR-0444
ECG-CONN ECG-CONN1
UR-0445
ECG-CONN2
UR-04301 No TEMP/NIBP/MP ch 1
MP1 UR-0455
MP2/NIBP
UR-3908
SpO2 board
UR-0431
REC/EXT
HV-831V UR-0420
Biphasic HV unit HV SW
UR-0418
HV CPU
WS-831V UR-0419
Recorder unit Motor assy
(WS-252V)

1. GENERAL
TEC-8322 1
TEC-8322
Defibrillator
UR-0414
CONTROL
UR-04151 No PACER
ECG/PACER
KEY/LED UR-0452
KEY/LED1
UR-0453
KEY/LED2
UR-0417
POWER
UR-0429 UR-0444
ECG-CONN ECG-CONN1
UR-0445
ECG-CONN2
UR-04302 No NIBP
MP2/TEMP UR-0455
MP2/NIBP
UR-3908
UR-0454
SpO2 board
TEMP
UR-0431
REC/EXT
HV-831V UR-0420
UR-0418
HV CPU
WS-831V UR-0419
(WS-252V)

1. GENERAL
TEC-8332
TEC-8332
Defibrillator
UR-0414
CONTROL
UR-0415
ECG/PACER
UR-0416
KEY/LED UR-0452
KEY/LED1
UR-0453
KEY/LED2
UR-0417
POWER
UR-0429 UR-0444
ECG-CONN ECG-CONN1
UR-0445
ECG-CONN2
UR-04302 No NIBP
MP2/TEMP UR-0455
MP2/NIBP
UR-3908
UR-0454
SpO2 board
TEMP
UR-0431
REC/EXT
HV-831V UR-0420
UR-0418
HV CPU
WS-831V UR-0419
(WS-252V)

1. GENERAL
TEC-8342 1
TEC-8342
Defibrillator
UR-0414
CONTROL
UR-04151 No PACER
ECG/PACER
KEY/LED UR-0452
KEY/LED1
UR-0453
KEY/LED2
UR-0417
POWER
UR-0429 UR-0444
ECG-CONN ECG-CONN1
UR-0445
ECG-CONN2
UR-0430 UR-0455
MP2/NIBP/TEMP MP2/NIBP
UR-0454
UR-3908 TEMP
SpO2 board
UR-0431
REC/EXT
HV-831V UR-0420
UR-0418
HV CPU
WS-831V UR-0419
(WS-252V)

1. GENERAL
TEC-8352
TEC-8352
Defibrillator
UR-0414
CONTROL
UR-0415
ECG/PACER
UR-0416 UR-0452
KEY/LED KEY/LED1
UR-0453
KEY/LED2
UR-0417
POWER
UR-0429 UR-0444
ECG-CONN ECG-CONN1
UR-0445
ECG-CONN2
UR-0430 UR-0455
MP2/NIBP/TEMP MP2/NIBP
UR-0454
UR-3908 TEMP
SpO2 board
UR-0431
REC/EXT
HV-831V UR-0420
UR-0418
HV CPU
WS-831V UR-0419
(WS-252V)

AC-831V
12 lead ECG unit UR-0428
12L-ECG 1. GENERAL
QI-831V
Options 1
AUXOUT unit UR-0426
AC-831V AUXOUT
12 lead ECG unit UR-0428
QI-832V
12L-ECG
Bluetooth module UR-0427
QI-831V Bluetooth adapter
AUXOUT unit UR-0426
QI-833V AUXOUT
ZS interface unit UR-4100
QI-832V ZSIF BD
Bluetooth
ZS-900Pmodule UR-0427
Transmitter Bluetooth adapter
ND-831V
QI-833V UR-0437 UR-0442
External paddles
ZS interface unit EXT_PADDLE
UR-4100 EXT_PDL_APEX
ZSIF BD
ZS-900P UR-0443
Transmitter ND-618V EXT_PDL_STERNUM
Adult electrode assy
ND-831V
DP-831VK UR-0437 UR-0442
External paddles
External paddles EXT_PADDLE EXT_PDL_APEX
UR-0315
holder
TEST LOAD
UR-0443
SC-831V
ND-618V EXT_PDL_STERNUM
AC/DC module
Adult electrode assy
DP-831VK
ND-863V
Externalpaddle
Internal paddles
electrode ø35
UR-0315
holder
TEST LOAD
ND-864V
SC-831V
Internal paddle electrode ø45
AC/DC module
ND-865V
ND-863V
ND-866V
ND-864V
ND-867V
ND-865V
ND-866V
ND-867V

1. GENERAL
ND-893V QP-551VK
Internal paddle electrode ø35 with SW Defibrillation report software
ND-894V QS-831V
Internal paddle electrode ø45 with SW Upgrade kit
ND-895V YS-003V5
Internal paddle electrode ø55 with SW Upgrade kit
ND-896V YZ-047H4
Internal paddle electrode ø65 with SW Bed rail hook
ND-897V SB-831V
Internal paddle electrode ø75 with SW Battery pack
JC-855V SB-801V
Pad adapter Battery charger
JC-865V KG-831V

Pad adapter Wall mount
P-510 KG-832V
Disposable paddles Wall mount
P-512 DI-831V
Disposable paddles Basket
P-711 KD-831V
Disposable paddles Cart
P-713 YZ-025H0
Disposable paddles Paste holder kit
AX-250V
Test load unit
AX-251V
Test load unit

1. GENERAL
1
Board and Unit Location
MP/TEMP/NIBP board POWER board

LED DRIVER board
SpO2 board
KEY/LED board
ECG/PACER board POWER

board
CONTROL board
ECG-CONN board
KEY/LED board
POWER board
ECG-CONN board
REC/EXT board
KEY/LED board KEY/LED board

1. GENERAL
TEST LOAD
AUXOUT unit
BIPHASIC HV unit BLUETOOTH module
AC/DC module
HV CPU board
12LEAD ECG unit
SPEAKER RECORDER unit
LCD unit

Section 2 Troubleshooting
2
How to Troubleshoot............................................................................................................................................. 2.2

Error Code............................................................................................................................................................ 2.3
Defibrillation............................................................................................................................................... 2.4
Operation Panel......................................................................................................................................... 2.5
Communication.......................................................................................................................................... 2.6
Data Error................................................................................................................................................... 2.7
Pacing (TEC-8332/TEC-8352 Only)........................................................................................................... 2.7
12 Lead ECG Measurement (When Using the Optional AC-831V 12 Lead ECG Unit)............................. 2.8
Message............................................................................................................................................................... 2.9
Defibrillation and Cardioversion................................................................................................................. 2.9
AED.......................................................................................................................................................... 2.10
Pacing...................................................................................................................................................... 2.10
Monitoring................................................................................................................................................ 2.11
ECG............................................................................................................................................... 2.11
SpO2 .............................................................................................................................................. 2.12
CO2 ................................................................................................................................................ 2.13
Invasive Blood Pressure................................................................................................................. 2.13
NIBP............................................................................................................................................... 2.13
Temperature................................................................................................................................... 2.14
System..................................................................................................................................................... 2.16
General.......................................................................................................................................... 2.16
Battery............................................................................................................................................ 2.16
Recording....................................................................................................................................... 2.17
Bluetooth........................................................................................................................................ 2.17
Troubleshooting.................................................................................................................................................. 2.18
General..................................................................................................................................................... 2.18
Defibrillation............................................................................................................................................. 2.19
Pacing (TEC-8332/TEC-8352 Only)......................................................................................................... 2.20
Monitoring................................................................................................................................................ 2.20
ECG............................................................................................................................................... 2.20
SpO2 .............................................................................................................................................. 2.21
CO2 ................................................................................................................................................ 2.22
NIBP............................................................................................................................................... 2.23
Blood Pressure (PRESS)............................................................................................................... 2.24
Temperature................................................................................................................................... 2.24
Recording................................................................................................................................................. 2.24
Battery...................................................................................................................................................... 2.25
SD Card.................................................................................................................................................... 2.25

2. TROUBLESHOOTING
How to Troubleshoot
Use this section to locate, identify and solve a problem in the defibrillator or an
error message displayed on the screen. The troubleshooting tables in this section
are divided into general problems and displayed error messages.
1. Determine which troubleshooting table to use. Also refer to “Messages and

Troubleshooting” in Section 8 of the Operator’s Manual Part I.
2. In the “Error Code”, “Message” or “Problem” column, find the trouble item
that matches the problem or error message.
3. Do the action recommended in the “Action” column. (Do the first action
recommended in the “Action” column.)
4. If the problem or error message is not solved, do the next action

recommended in the “Action” column. (If this does not solve the problem,
do the next recommended sections.)
NOTE
Before contacting your Nihon Kohden representative for technical
support, please complete a copy of the Maintenance Check Sheet (the
original copy is provided at the end of the Section 4 “Maintenance”),
and if possible, provide additional detailed information on the problem.
Send the complete copy of the Maintenance Check Sheet to your Nihon
Kohden representative. This will allow your Nihon Kohden representative
to provide you with the best support.

2. TROUBLESHOOTING
Error Code
2
The defibrillator displays an error code if it detects an error when the power is
turned on and during operation.
NOTE
• For problems that are not reproducible, call up the SYSTEM SETUP
– 7. DEVICE HISTORY screen and print the MAINTENANCE REPORT.
Refer to the Administrator’s Guide for the detail of this procedure. The
error code will be lost when the power is turned off.
• Always check all the cable connections in the defibrillator before
performing the action recommended in the troubleshooting tables in
this section. This is because a loose cable connection can cause the
defibrillator to display the error code.
An error code is displayed.

ERROR AXXX
ERROR CXXX
ERROR DXXX
ERROR KXXX
ERROR PXXX
ERROR TXXX
Turn off the instrument, then turn on the instrument and do the same operation.
Error AXXX, CXXX, DXXX and

The error code is saved KXXX:
Is the error code No No
in the “MAINTENANCE Perform charge/discharge test.
displayed? Error PXXX
REPORT”?
Perform pacing test.
Error TXXX
Yes Yes
Perform 12L-ECG test.
Is the error code No Instrument is normal.

displayed? But find the cause of the error code.
Yes
Refer to error code
description for detail.

2. TROUBLESHOOTING
Defibrillation
Error Code Meaning Possible Cause Action

A501 During standby mode, the HV capacitor Faulty biphasic HV unit. Replace the biphasic HV unit.
has more than 1 J energy for more than one Faulty HV CPU board. Replace the HV CPU board.
second.
A512 When charging is started, the HV capacitor Faulty biphasic HV unit. Replace the biphasic HV unit.
energy did not reach 1 J within 2 seconds. Faulty HV capacitor. Replace the HV capacitor.
Faulty HV CPU board. Replace the HV CPU board.
A513 The energy does not reach the selected Faulty biphasic HV unit. Replace the biphasic HV unit.
energy within the specified time. Faulty HV capacitor. Replace the HV capacitor.
A524 After charging, the capacitor energy Faulty biphasic HV unit. Replace the biphasic HV unit.
decreases the specified value for each Faulty HV capacitor. Replace the HV capacitor.
energy. Faulty HV CPU board. Replace the HV CPU board.
A527 After charging, the capacitor energy is about Faulty biphasic HV unit. Replace the biphasic HV unit.
15% above the selected energy. Faulty HV CPU board. Replace the HV CPU board.
A529 After charging, the actual charged energy is Faulty biphasic HV unit. Replace the biphasic HV unit.
different from the selected energy. Faulty HV CPU board. Replace the HV CPU board.
A552 The switch that controls output from HV Faulty biphasic HV unit. Replace the biphasic HV unit.
unit is faulty. Faulty CONTROL board. Replace the CONTROL board.
A556 Internal discharge takes more than 20 Faulty biphasic HV unit. Replace the biphasic HV unit.
seconds to complete. Faulty CONTROL board. Replace the CONTROL board.
A566 HV capacitor’s voltage did not reach its Faulty biphasic HV unit. Replace the biphasic HV unit.
target value 20 seconds after adjusted Faulty HV CPU board. Replace the HV CPU board.
internal discharge.
A570 HV monitoring error signal is detected. Faulty biphasic HV unit. Replace the biphasic HV unit.
Faulty CONTROL board. Replace the CONTROL board.
A585 The voltage of the HV capacitor exceeds its Faulty biphasic HV unit. Replace the biphasic HV unit.
specified voltage. Faulty CONTROL board. Replace the CONTROL board.
A587 When the disposable pad is used, 12.5% Faulty biphasic HV unit. Replace the biphasic HV unit.
or more of the charged energy remains in Faulty CPU board. Replace the CPU board.
the HV capacitor 2 seconds after external Faulty HV CPU board. Replace the HV CPU board.
discharge.
A597 When discharging, the second phase pulse Faulty biphasic HV unit. Replace the biphasic HV unit.
is not output. Faulty CONTROL board. Replace the CONTROL board.

2. TROUBLESHOOTING
Operation Panel
NOTE
• When the power is on and the following key switch is pressed and held
2
for more than 10 seconds, the error code of each key is displayed.
• If the key was not pressed and held, check each key function with the
System Maintenance screen. Refer to “System Maintenance Screen –
Check Hardware Screen – Check Key Screen” in Section 4.

K503 The silence alarm key error is Faulty KEY/LED board. Replace the KEY/LED board.
detected. Faulty CONTROL board. Replace the CONTROL board.
K505 The record/stop key error is detected. Faulty KEY/LED board. Replace the KEY/LED board.
K507 The SYNC button error (front panel) Faulty KEY/LED board. Replace the KEY/LED board.
is detected. Faulty CONTROL board. Replace the CONTROL board.
K508 The CHARGE/AED button error Faulty KEY/LED board. Replace the KEY/LED board.
(front panel) is detected. Faulty CONTROL board. Replace the CONTROL board.
K509 The SHOCK button error (front Faulty KEY/LED board. Replace the KEY/LED board.
panel) is detected. Faulty CONTROL board. Replace the CONTROL board.
K511 The CHARGE/AED button error Faulty external paddles. Replace the external paddles.
(apex external paddle) is detected. Faulty CONTROL board. Replace the CONTROL board.
K512 The SHOCK button error (apex Faulty external paddles. Replace the external paddles.
external paddle) is detected. Faulty CONTROL board. Replace the CONTROL board.
K513 The SHOCK button error (sternum Faulty external paddles. Replace the external paddles.
external paddle) is detected. Faulty CONTROL board. Replace the CONTROL board.
K516 The PACING START/STOP key Faulty KEY/LED board. Replace the KEY/LED board.
error is detected. Faulty CONTROL board. Replace the CONTROL board.
K517 PACING RATE Up key error Faulty KEY/LED board. Replace the KEY/LED board.
K518 PACING RATE Down key error Faulty KEY/LED board. Replace the KEY/LED board.
K519 PACING CURRENT Up key error Faulty KEY/LED board. Replace the KEY/LED board.
K520 PACING CURRENT Down key Faulty KEY/LED board. Replace the KEY/LED board.
error Faulty CONTROL board. Replace the CONTROL board.
K524 CHILD MODE button error Faulty KEY/LED board. Replace the KEY/LED board.
K531 F1 key error Faulty KEY/LED board. Replace the KEY/LED board.

2. TROUBLESHOOTING
Communication

C507 When the power is turned on, the Faulty CONTROL board. Replace the CONTROL board.
communication error between the RTC
(real time clock) and main CPU is
detected for one second.
C508 The 12 LEAD ECG board does not Faulty 12 lead ECG unit. Replace the 12 lead ECG unit.
respond. Faulty CONTROL board. Replace the CONTROL board.
C511 The sub CPU does not update the data in Faulty CONTROL board. Replace the CONTROL board.
the DPRAM for one second.
C514 The pacing CPU does not update the data Faulty ECG/PACER board. Replace the ECG/PACER
in the DPRAM for one second. board.
C515 The HV CPU does not update the data in Faulty HV CPU board. Replace the HV CPU board.
the DPRAM for one second. Faulty CONTROL board. Replace the CONTROL board.
C516 RTC backup battery is detected to be Faulty CONTROL board. Replace the CONTROL board.
empty.
C517 I2C bus error for communication with the Faulty battery pack. Replace the battery pack.
battery memory (CPU) of the battery pack Faulty CONTROL board. Replace the CONTROL board.
in slot A is detected.
C518 I2C bus error for communication with the Faulty battery pack. Replace the battery pack.
battery memory (CPU) of the battery pack Faulty CONTROL board. Replace the CONTROL board.
in slot B is detected.
C519 • The MP unit does not respond for more Faulty MP board. Replace the MP board.
than 4 seconds. Faulty CONTROL board. Replace the CONTROL board.
• When turning the defibrillator on,
information reception retry for the
system information sent after releasing
the MP unit reset failed three times.
C521 Bluetooth® module does not respond. Faulty Bluetooth® module. Replace the Bluetooth® module.
C522 E-CPU does not respond. Faulty ECG/PACER board. Replace the ECG/PACER
board.

2. TROUBLESHOOTING
Data Error
Error Code Meaning Possible Cause Action 2

D501 Data in the DRAM or flash memory is not Faulty DRAM or flash Replace the CONTROL board.
read out correctly (summation error). memory.
D511 When the power is turned on, settings After settings in the Perform the “Flash Save”
in the System Maintenance screen do System Maintenance procedure in the System
not match the backup data in the flash screen are changed, the Maintenance screen.
memory. “Flash Save” procedure is
not performed.
During power off Delete the report data in the
sequence, power down System Setup screen.
occurs.
D512 When the power is turned on, damaged During power off Delete the report data in the
waveform report data in the flash memory sequence, power down System Setup screen.
is detected. occurs.
Pacing (TEC-8332/TEC-8352 Only)

P501 Actual pacing output rate is 12.5% above Faulty ECG/PACER board. Replace the ECG/PACER
or below the setting rate. board.
P502 Pulse width of the pacing output pulse is Faulty ECG/PACER board. Replace the ECG/PACER
larger or smaller than the selected width. board.
P503 Current intensity of the pacing output Faulty ECG/PACER board. Replace the ECG/PACER
pulse is larger than the selected value. board.
P504 Current intensity of the pacing output Faulty ECG/PACER board. Replace the ECG/PACER
pulse is smaller than the selected value. board.
P505 Pacing output that is not requested by the Faulty ECG/PACER board. Replace the ECG/PACER
CPU is detected. board.
P506 Pacing output voltage exceeds the upper Faulty ECG/PACER board. Replace the ECG/PACER
limit. board.
P511 Error was detected in the short-mode of Faulty ECG/PACER board. Replace the ECG/PACER
the transistor. board.

2. TROUBLESHOOTING
12 Lead ECG Measurement (When Using the Optional AC-831V 12 Lead ECG Unit)

T500 Serial communication error on the 12 lead Faulty 12 lead ECG unit. Replace the 12 lead ECG unit.
ECG unit.
T502 Data of the 12 lead ECG unit is out of Faulty 12 lead ECG unit. Replace the 12 lead ECG unit.
range.
T506 Timer error of the 12 lead ECG unit. Faulty 12 lead ECG unit. Replace the 12 lead ECG unit.
T516 Write error of the flash memory on the 12 The defibrillator was not Correctly turn the defibrillator
lead ECG unit. correctly turned off. off.
(Power cord was
disconnected or battery pack
was removed while turning
the defibrillator off and an
error occurred while turning
the defibrillator off.)
Faulty 12 lead ECG unit. Replace the 12 lead ECG unit.
T521 Time out of the 12 lead ECG unit Faulty 12 lead ECG unit. Turn the power off, then retry
analysis. the 12 lead ECG analysis. If
the error code appears again,
replace the 12 lead ECG unit.

2. TROUBLESHOOTING
Message
2
Defibrillation and Cardioversion
Message Description Action

CHECK PADS In manual defibrillation or AED mode, the • Shave hair on the skin where pads are
contact impedance of the disposable pads is placed, then firmly attach the disposable
too high. pads to the patient chest.
When PAD lead is selected, disposable pads • Firmly connect the pad adapter and
are not attached to the patient firmly. disposable pads.
The pad adapter is disconnected from the Firmly connect the pad adapter and
disposable pads. disposable pads.
CONNECT PADS/ In manual defibrillation mode, paddles or pad Connect the paddles or pad adapter to the
PADDLES adapter are not connected to the defibrillator. defibrillator.
CN1204 harness is disconnected or broken. Connect the CN1204 harness to the connector
on the board.
Check the continuity of the CN1204 harness.
Paddle connector pin is broken or bent. • Replace the paddles.
• Replace the paddle connector of the
defibrillator.
If the message appears when the paddles/pads Replace the CONTROL board.
are connected to the defibrillator, CONTROL
board is faulty.
ENERGY WAS NOT There is remaining energy in the defibrillator 2 Check the paddle or pad connection.
DELIVERED TO seconds after defibrillation was performed. The
PATIENT remaining energy is internally discharged.
HIGH IMPEDANCE Skin-paddle contact impedance is too high. Press the paddles onto the patient firmly.
LOW IMPEDANCE Skin-paddle contact impedance is too low. Check that the paddles or pads do not touch
each other.
HV MONITOR ERROR • Faulty biphasic HV unit. • Replace the biphasic HV unit.
• Faulty HV CPU board. • Replace the HV CPU board.
RELAY DRIVE ERROR • Faulty biphasic HV unit. • Replace the biphasic HV unit
Set energy to 50 J or less Above 50 J is selected when the internal Turn the control dial to 50 J or less.
paddles are connected to the defibrillator.
on the board.
defibrillator.

2. TROUBLESHOOTING
AED

Could not analyze ECG. In AED mode, the defibrillator cannot analyze • Following the instruction, start CPR.
ECG due to noise. • If possible, remove cause of noise. When
the CPR is necessary, make CPR a priority
over removing noise.
If the message still appears when cause of
noise is removed:
• ECG/PACER board is faulty. • Replace the ECG/PACER board.
• CONTROL board is faulty. • Replace the CONTROL board.
CHECK PADS • The pads are disconnected from the pad • Connect the pads to the pad adapter.
adapter.
• The pads are not properly attached to the • Properly attach the pads to the patient.
patient.
CONNECT PADS In AED mode, the pad adapter is not connected Connect the pad adapter to the defibrillator.
to the defibrillator.
on the board.
defibrillator.
If the message appears when the paddles/pads Replace the CONTROL board.
are connected to the defibrillator, CONTROL
board is faulty.
HIGH IMPEDANCE Skin-paddle contact impedance is too high. Press the paddles onto the patient firmly.
LOW IMPEDANCE Skin-paddle contact impedance is too low. Check that the pads do not touch each other.
USE DISPOSABLE In AED mode, only disposable pads are Use disposable pads in AED mode.
PADS available. External paddles and internal
paddles are not available.
Pacing

CHECK PADS The pad adapter is disconnected from the Firmly connect the pad adapter and
disposable pads. disposable pads.
In FIXED or DEMAND pacing mode, the Firmly attach the disposable pads to the
disposable pad is not firmly attached to the patient chest.
patient.
Pacing stopped Pacing stopped because:
(ECG lead disconnected) • An electrode lead is disconnected from an • Properly connect the electrode lead to the
electrode. ECG electrode.
• An electrode is detached from the patient. • Replace the electrodes with new ones.
• Electrode lead is disconnected from the • Properly connect the electrode lead to the
connection cable. connection cable.
• Bad contact between the electrode and lead • Replace the electrode lead with a new one.
clip.
• Electrode lead discontinuity. • Replace the electrode lead with a new one.
• Abnormally high polarization voltage. • Replace the electrodes with new ones.
When none of above occurred, ECG/PACER When none of above solve the problem,
board is faulty. ECG/PACER board is faulty. Replace the
ECG/PACER board.

2. TROUBLESHOOTING

Pacing stopped Pacing stopped because:
(pad disconnected) • The pad adapter is disconnected from the • Firmly connect the pads to the pad adapter. 2
disposable pads or the defibrillator. Firmly connect the pad adapter to the
paddle connector of the defibrillator.
• The disposable pads are detached from the • Attach the disposable pads to the patient.
patient.
When none of above occurred, ECG/PACER When none of above solve the problem,
board is faulty. ECG/PACER board is faulty. Replace the
ECG/PACER board.
USE DISPOSABLE In FIXED or DEMAND pacing mode, only Use disposable pads in pacing mode.
PADS disposable pads are available. External paddles
and internal paddles are not available.
Monitoring
ECG

CANNOT ANALYZE Noise interference for more than 30 seconds Remove noise.
and heart rate cannot be counted and
arrhythmia cannot be analyzed.
If the message still appears when cause of
noise is removed:
• ECG/PACER board is faulty. • Replace the ECG/PACER board
• CONTROL board is faulty. • Replace the CONTROL board.
CHECK Ca Ca electrode is detached from the patient. Attach the Ca electrode to the patient.
ELECTRODE
CHECK Cb Cb electrode is detached from the patient. Attach the Cb electrode to the patient.
ELECTRODE
ECG: CHANGE An electrode is deteriorated. Replace the electrode with a new one.
ELECTRODES
ECG: CHANGE PADS The disposable pads are deteriorated. Replace the pads with new ones.
ECG: CHECK CHEST The chest electrode is detached from the Properly attach the electrode to the patient.
ELECTRODES patient. If the electrode cannot be attached firmly,
replace the electrode.
ECG: CHECK The electrode is detached from the patient. Properly attach the electrode to the patient.
ELECTRODES If the electrode cannot be attached firmly,
replace the electrode.
The electrode lead is disconnected from the Connect the electrode lead to the ECG
ECG connection cord. connection cord.
The clip of the lead is not properly attached to Properly attach the clip to the electrode.
the electrode.
Broken electrode lead Replace the electrode lead.
The external ECG cable is disconnected from Connect the external ECG cable.
the defibrillator.
ECG: CHECK PADS The disposable pad is detached from the When using the disposable pads, attach the
patient or paddles used for ECG monitoring disposable pads to the patient or replace the
are not placed on the patient properly. disposable pads with the new ones.
When using the paddles, place the paddles on
the patient.

2. TROUBLESHOOTING

ECG: CONNECT PADS/ When PADDLE lead is selected in the Connect the paddles or pad adapter to the
PADDLES monitor mode, paddles or pad adapter are not defibrillator.
connected to the defibrillator.
When the paddles or pads are connected to the Replace the CONTROL board.
defibrillator, CONTROL board is faulty.
on the board.
defibrillator.
F (LL) LEAD OFF LL electrode is detached from the patient. Attach the LL electrode to the patient.
L (LA) LEAD OFF LA electrode is detached from the patient. Attach the LA electrode to the patient.
LIMB LEAD OFF Limb electrode is detached from the patient. Attach the limb electrode to the patient.
R (RA) LEAD OFF RA electrode is detached from the patient. Attach the RA electrode to the patient.
V1 (C1) LEAD OFF V1 (C1) electrode is detached from the patient.
Attach the electrode to the patient.
SpO2

SpO2: CHECK PROBE The probe is detached from the patient. Check the probe attachment condition and
remove the cause.
The probe is disconnected from the SpO2 Securely connect the probe to the SpO2
connection cord. connection cord.
When the SpO2 probe is correctly connected: Replace the SpO2 board and/or MP board.
• SpO2 board is faulty.
• MP board is faulty.
SpO2: CHECK PROBE SpO2 probe is deteriorated. Replace the probe with a new one.
SITE
SpO2: CONNECTOR Connector of the SpO2 connection cord is Check the connection of the SpO2 connection
OFF disconnected. cord.
If the SpO2 connection cable is properly If it does not solve the problem:
connected:
• SpO2 board is faulty. • Replace the SpO2 board.
• MP board is faulty. • Replace the MP board.
SpO2: CORD SpO2 probe is disconnected from the Connect the SpO2 probe to the connection
DISCONNECTED connection cable. cable.
SpO2: LIGHT Too much light on the probe. Remove light or cover the probe site with
INTERFERENCE blanket.
SpO2: LOW QUALITY Considerable body movement. When the message is displayed frequently,
SIGNAL The probe is not attached to the patient check the patient condition and, if necessary,
properly. change the attachment site.
SpO2: MODULE ERROR Faulty SpO2 board. Replace the SpO2 board.
SpO2: PROBE ERROR The probe lifetime is expired. Replace the probe with a new one.
Probe discontinuity or short-circuit. Replace the probe with a new one.
Faulty SpO2 connection cord. Replace the SpO2 connection cord with a new
one.
Faulty SpO2 probe. Replace the SpO2 probe with a new one. If
the message still appears, replace the SpO2
adapter.

2. TROUBLESHOOTING
CO2

CO2: APNEA Respiration was not detected for the period
2
set on the CO2 SETUP window for CO2 alarm —
settings.
CO2: 2 SENSORS Two CO2 sensors are connected to the Disconnect one of the CO2 sensors.
CONNECTED defibrillator.
CO2: CHANGE The CO2 adapter is damaged, deteriorated or Replace the CO2 adapter with a new one.
ADAPTER the cable is broken.
CO2: CHECK SENSOR Insufficient sensor light. Refer to the CO2 sensor kit manual. If
necessary, replace the kit with a new one.
CO2: CONNECTOR OFF The CO2 sensor kit is disconnected from the Connect the CO2 sensor kit properly. When
defibrillator. CO2 monitoring is not necessary, press the
Silence Alarms key to silence the alarm.
The CO2 sensor kit is damaged. Replace the CO2 sensor kit with a new one.
When the CO2 sensor kit is correctly connected Replace the MP board.
and the CO2 sensor kit is not deteriorated, MP
board is faulty.
CO2: SENSOR ERROR CO2 sensor is damaged, deteriorated or cord is Replace the CO2 sensor with a new one.
broken.
When the CO2 sensor kit is not damaged or Replace the MP board.
deteriorated or cord is not broken, MP board is
faulty.
Invasive Blood Pressure

PRESS: CHECK The blood pressure transducer is disconnected Connect the blood pressure transducer to
SENSOR from the invasive blood pressure connection the invasive blood pressure connection cord
cord. properly.
Malfunction of the blood pressure transducer. Replace the blood pressure transducer with a
new one.
The invasive blood pressure connection cord is Replace the invasive blood pressure
damaged. connection cord with a new one.
When the transducer is properly connected Replace the MP board.
and is not faulty, and connection cord is not
damaged, MP board is faulty.
PRESS: CONNECTOR The PRESS connection cord is disconnected Connect the PRESS connection cord
OFF from the defibrillator. properly.
When PRESS monitoring is not necessary,
press the Silence Alarms key to silence the
alarm.
The PRESS connection cord is damaged. Replace the PRESS connection cord with a
new one.
When the PRESS connection cord is properly Replace the MP board.
connected to the defibrillator and is not
damaged, MP board is faulty.
PRESS: LABEL More than one invasive blood pressure Set another label.
ALREADY USED connection cord with the same label are used.
NIBP

CANNOT USE NEO An NIBP cuff for neonate is connected. An NIBP cuff for neonate cannot be used.
CUFF Use an NIBP cuff for adult or child.

2. TROUBLESHOOTING

NIBP: AIR LEAK The cuff or air hose is not connected properly.
Connect the cuff to the air hose properly.
Connect the air hose to the socket on the
defibrillator left side panel properly.
The cuff or air hose is damaged. Replace the cuff or air hose with a new one.
NIBP: CANNOT The patient’s pulse wave is small. Measure by palpation or invasive blood
DETECT PULSE pressure method.
The cuff is not wrapped on the patient Wrap the cuff around the arm of the patient
correctly. properly.
NIBP: CHECK NIBP is measured at 1 minute intervals for Check the patient condition and determine
INTERVAL SETTINGS more than 30 minutes. whether to continue measuring NIBP at 1
minute intervals.
NIBP: CONNECTOR The air hose is disconnected from the Connect the air hose properly. When NIBP
OFF defibrillator. monitoring is not necessary, press the Silence
Alarms key to silence the alarm.
The air hose is damaged. Replace the air hose with a new one.
When the air hose is properly connected, NIBP Replace the NIBP board.
board is faulty.
NIBP: CUFF The air hose is bent or squeezed. Check that the air hose is not bent or
OCCLUSION squeezed.
NIBP: HIGH CUFF Extreme pressure was applied to the cuff. Remove the cause.
PRESS
NIBP: MEAS TIMEOUT The measuring time exceeded the specified If the cause is arrhythmia, measure by
time due to arrhythmia or noise. invasive blood pressure measurement.
Remove the cause if due to noise.
NIBP: MODULE NIBP board is faulty. Replace the NIBP board.
ERROR
NIBP: SAFETY The hose is bent. Check that the hose is not bent.
CIRCUIT RUNNING The inflation time is too long. Stop measurement.
(When this message is In auto mode measurement, the cuff inflation Stop measurement.
displayed, measurement started before the cuff deflation is complete.
cannot be performed for
40 seconds.)
NIBP: SYSTOLIC The maximum blood pressure exceeded 290 Measure by palpation or the invasive blood
OVER mmHg when using the adult/child cuff. pressure method.
Temperature

TEMP: 2 Two TEMP connection cords (JT-900P) are Only one TEMP connection cord (JT-900P)
CONNECTORS USED connected to both MULTI sockets on the can be used with the MULTI socket at a time.
defibrillator. Disconnect unnecessary connection cord.
Thermistor probe is connected to the TEMP When a thermistor probe is connected to
modular jack and the JT-900P TEMP the TEMP modular jack, thermistor probe
connection cord is connected to the one of the with the JT-900P TEMP connection cord
MULTI connectors. cannot be used. Disconnect the JT-900P
TEMP connection cord or thermistor probe
connected to the TEMP modular jack.
TEMP: CHECK The probe is disconnected from the modular Connect the probe to the modular jack or the
SENSOR jack or the temperature connection cord is temperature connection cord to the MULTI
disconnected from the MULTI socket. socket properly.
The probe or temperature connection cord is Replace the probe or temperature connection
damaged. cord with a new one.
The measured value is outside the measuring Check the probe attachment site.
range.

2. TROUBLESHOOTING

TEMP: CONNECTOR The temperature connection cord is Connect the temperature connection cord
OFF disconnected from the defibrillator. properly. When temperature monitoring is not 2
necessary, press the Silence Alarms key to
silence the alarm.
The temperature connection cord is damaged. Replace the temperature connection cord with
a new one.
When the temperature connection cord is Replace the TEMP board.
properly connected and is not damaged, TEMP
board is faulty.
TEMP: LABEL More than one temperature probe with the Set another label.
ALREADY USED same label are used.

2. TROUBLESHOOTING
System
General

Defibrillator error. Use HV error is found during basic checks. • Replace the biphasic HV unit.
another defibrillator. • Replace the HV CPU board.
An error that prevents defibrillation occurs. • Replace the biphasic HV unit.
• Replace the HV CPU board.
• Replace the CONTROL board.
ERROR A××× Faulty HV. Refer to “Error Code” in this section.
ERROR C××× Communication error.
ERROR D××× Faulty ROM/RAM.
ERROR K××× Faulty keys.
ERROR P××× Faulty pacing unit.
ERROR T××× Faulty 12 lead ECG unit.
HV MONITOR ERROR • Faulty biphasic HV unit. • Replace the biphasic HV unit.
MP MODULE ERROR Faulty MP board. Replace the MP board.
Overheating Charging (for defibrillation or cardioversion) Turn the control dial to the OFF position
more than 20 times in 20 minutes. to turn the defibrillator off and leave the
defibrillator for 20 minutes. Then turn on the
defibrillator. In an emergency, you can use the
defibrillator even if this message is displayed.
PARAMETER NOT The connector of a device that is not available Use parameters that are available for TEC-
AVAILABLE for the TEC-8300 series defibrillator is 8300 series defibrillator.
connected.
RELAY DRIVE ERROR • Faulty biphasic HV unit. • Replace the biphasic HV unit.
Battery

ABNORMAL VOLTAGE Abnormal battery power is detected in the Replace the battery pack in battery slot A.
(SLOT A) battery pack in battery slot A.
ABNORMAL VOLTAGE Abnormal battery power is detected in the Replace the battery pack or AC/DC module
(SLOT B) battery pack or AC/DC module in battery slot in battery slot B.
B.
BATTERY A NOT The battery pack in battery slot A is not Perform battery calibration to calibrate the
CALIBRATED calibrated for 6 months (180 days). battery pack.
BATTERY B NOT The battery pack in battery slot B is not Perform battery calibration to calibrate the
CALIBRATED calibrated for 6 months (180 days). battery pack.
BATTERY CHARGE • Faulty battery pack. • Replace the battery pack.
ERROR • Faulty POWER board. • Replace the POWER board.
BATTERY PACK Unused battery pack in slot A consumes a Replace the battery pack in the battery slot A.
ERROR (SLOT A) certain amount of battery power.
BATTERY PACK Unused battery pack in slot B consumes a Replace the battery pack in the battery slot B.
ERROR (SLOT B) certain amount of battery power.
BATTERY PACK (SLOT A battery pack that is not initialized is in the Replace the battery pack in the battery slot A.
A) NOT INITIALIZED battery slot A.
BATTERY PACK (SLOT A battery pack that is not initialized is in the Replace the battery pack in the battery slot B.
B) NOT INITIALIZED battery slot B.
BOTH BATTERIES A Both batteries in battery slots A and B are low. Replace the battery packs with fully charged
AND B ARE LOW ones or use the AC/DC module.

2. TROUBLESHOOTING

BATTERY TEMP OUT Abnormal temperature is detected in the When using two battery packs, remove the
OF RANGE (SLOT A) battery pack in battery slot A. battery pack in the battery slot A. When 2
using the optional AC/DC module, put
the defibrillator in a place at the specified
temperature range and wait until the message
disappears.
BATTERY TEMP OUT Abnormal temperature is detected in the Remove the battery pack in the battery slot B.
OF RANGE (SLOT B) battery pack in battery slot B.
CHARGE BATTERY A Remaining battery power of the battery pack in Charge the battery pack with the AC/DC
battery slot A is low. module or replace the battery pack with the
fully charged one.
CHARGE BATTERY B Remaining battery power of the battery pack in Replace the battery pack with the fully
battery slot B is low. charged one.
CHARGE BATTERY Both battery packs are empty. Replace the battery packs with fully charged
IMMEDIATELY ones or use the AC/DC module to supply AC
power.
NO BATTERY IN SLOT The battery slot A is empty.
—
A
NO BATTERY IN SLOT The battery slot B is empty.
—
B
NOW OPERATING ON The defibrillator is switched to battery power
—
BATTERY A operation on the battery pack in battery slot A.
NOW OPERATING ON The defibrillator is switched to battery power
—
BATTERY B operation on the battery pack in battery slot B.
Recording

OUT OF PAPER Out of recording paper. Set a role of recording paper.
Recorder door is open. Press the recorder door until it clicks.
When the recording paper is set and the
recorder door is closed:
• The recorder unit is faulty. • Replace the recorder unit.
• The REC/EXT board is faulty. • Replace the REC/EXT board.
Bluetooth
The following messages appear only when installing the QI-832V Bluetooth®
module.

BLUETOOTH MODULE Bluetooth® module failure. Replace the Bluetooth® module.
ERROR

2. TROUBLESHOOTING
Troubleshooting
In the following tables, possible causes are listed in the order of most to least
likely.
General
Problem Possible Cause Action

The instrument heats up. The instrument is used for many hours. There is no abnormality in the
instrument. Turn the defibrillator off
and place it in a cooler place to cool
the defibrillator down.
Surrounding temperature is high. Check the surrounding temperature.
Faulty BIPHASIC HV unit. Replace the BIPHASIC HV unit.
Faulty POWER board. Replace the POWER board.
Faulty ECG/PACER board. Replace the ECG/PACER board.
Faulty AC/DC module. Replace the AC/DC module.
The defibrillator does not turn on. The power cord is disconnected. Firmly connect the power cord to the
AC outlet and the defibrillator.
The battery pack is not installed. Install the specified battery pack.
The battery pack is not locked. Push the battery pack until the latch
of the battery pack clicks.
Faulty LCD unit. Replace the LCD unit.
Faulty AC/DC module. Replace the AC/DC module with a
new one.
Faulty battery pack. Replace the battery pack with a new
one.
Faulty KEY/LED board. Replace the KEY/LED board.
The defibrillator turns off immediately Remaining power of the battery pack is Charge the battery pack.
after power on without user operation. low.
The defibrillator turns on but the Faulty CONTROL board. Replace the CONTROL board.
defibrillator does not start operation.
The defibrillator turns on when using a Faulty POWER board. Replace the POWER board.
battery pack in the one of two battery
slots but does not turns on using a
battery pack in another battery slot.
Screen is black. Waveform and Faulty LED DRIVER board. Replace LED DRIVER board.
characters are not seen. Faulty LCD unit. Replace the LCD unit.
Screen is white. Waveform and Faulty ECG/PACER board. Replace the ECG/PACER board.
characters are not seen. Faulty CONTROL board. Replace the CONTROL board.
Screen is dim. Waveform and characters Faulty LCD unit. Replace the LCD unit.
are not seen.
The printed date is JAN/01/80. The backup battery is almost discharged. Replace the CONTROL board.
(Under normal use condition, the
backup battery lifetime is at least 10
years.)
The report data are not saved. Faulty internal memory. Replace the CONTROL board.
On the REPORT SETUP window, the Deleted data cannot be recovered.
report data were deleted.

2. TROUBLESHOOTING

All settings set in the SETUP windows Faulty internal memory. Replace the CONTROL board.
and SYSTEM SETUP screen return 2
to the default settings without user
operation.
• When the battery is installed, the Power voltage changed. Confirm the AC power cord
defibrillator suddenly changes to connection and AC/DC module
battery operation from AC power installation. If connecting the power
operation. cord and correctly inserting the
• When the battery is not installed, the AC/DC module does not solve the
defibrillator suddenly turns off. problem, the AC/DC module or the
power cord is faulty. Replace the
AC/DC module or the power cord.
The date and time printed on the — Set the date and time.
recording paper is incorrect. The backup battery for the clock is Replace the CONTROL board.
discharged.
On the screen, there are some pixels For the TFT LCD screen, it is considered
which have randomly abnormal color or normal if some pixels have randomly —
do not light. abnormal color or do not light.
No sound is heard. Volume setting is low. Increase the volume on the
VOLUME window.
Faulty speaker or speaker cable Replace the speaker or speaker cable.
discontinuity.
No sound is heard when pressing the Faulty KEY/LED board. Replace the KEY/LED board.
button or key. Faulty CONTROL board. Replace the CONTROL board.
Defibrillation

While charging for defibrillation or In battery operation, the battery is Operate the defibrillator on AC
cardioversion, the defibrillator internally almost empty. power with the optional AC/DC
discharges the energy. module and recharge the battery.
The battery is automatically charged
when the defibrillator is connected to
AC power.
Faulty BIPHASIC HV unit. When an error code appears on the
(An error code appears on the screen.) screen, solve the problem referring
to the Defibrillation table in “Error
Code” in this section.
Cannot switch to synchronized mode. Appropriate lead is not selected. Change to the appropriate lead.
(There is key click sound.) You tried to perform synchronized On the PADDLE SETUP window,
cardioversion with the PADDLE lead set the “SYNC BY PADDLE” to
but synchronized cardioversion with ON.
the PADDLE lead is set to OFF on the
PADDLE SETUP window.
Cannot switch to synchronized mode. Faulty KEY/LED board. Replace the KEY/LED board.
(There is no key click sound.)
“0 J” is printed on the defibrillation TTR (transthoracic resistance) is 15 Ω Check that the paddles do not touch
report recording. or less. each other.
TTR (transthoracic resistance) is 255 Ω Press the paddles on the patient
or more. firmly.

2. TROUBLESHOOTING
Pacing (TEC-8332/TEC-8352 Only)

Although the PULSE lamp is lit, pacing Faulty ECG/PACER board. Replace the ECG/PACER board.
pulse does not appear on the ECG. Faulty CONTROL board. Replace the CONTROL board.
Although the START/STOP key is Pacing current is set to 0 mA. Set the appropriate pacing current
pressed, pacing does not start. with the PACING OUTPUT Up/
Down key.
In DEMAND mode, selected pacing rate Set the pacing rate appropriate for
is slower than the patient heart rate. the patient heart rate. When the
patient heart rate is slower than the
selected pacing rate, pacing pulse is
output automatically.
Monitoring
ECG

Dotted lines appear instead of the ECG • An ECG electrode is detached. Remove the cause. If it does not
waveforms. • An electrode lead is disconnected solve the problem, change the lead. If
from the electrode. changing the lead does not solve the
• The ECG connection cable is problem, replace the ECG/PACER
disconnected from the defibrillator. board.
• An electrode lead is faulty.
• The ECG/PACER board is faulty.
Baseline drifting. Patient body movement. Check the patient.
AC interference On the ECG SETUP window, HUM • On the ECG SETUP window, set
(50 or 60 Hz sine wave is superimposed FILTER is set to off. the HUM FILTER to on.
on the ECG waveform.) • Check if there is AC interference
with other instruments, and remove
the cause.
2-prong power cord is used. Use a 3-prong power cord.
AC Line Frequency settings on the Select the correct frequency for your
SYSTEM SETUP screen is not correct. country or area.
ECG waveform does not appear on the • Electrode lead discontinuity. Replace the electrodes or leads with
screen although electrodes are connected • Dirty electrode. new ones.
properly. New and old or different types of Use the same type of electrodes
electrodes are used together. which are purchased together.
No sync sound. Sync sound volume setting is low. Increase the volume on the
VOLUME window.
Sync source is set to “PRESS” or Set “SYNC SOURCE” to “ECG”.
“SpO2”.
discontinuity.
QRS sync mark is not displayed. On the ECG SETUP window, PACING • Remove the cause of the noise.
REJECT is set to ON and large • On the ECG SETUP window, set
amplitude AC interference noise is on PACING REJECT to OFF.
the ECG waveform.
Sync sound is irregular although there is Noise is misjudged to be QRS. Remove the cause of the noise.
no arrhythmia.

2. TROUBLESHOOTING

No alarm is generated. The Silence Alarms key on the Press the Silence Alarms key again.
defibrillator front panel is pressed. 2
On the SETUP window, alarm is set to On the SETUP window, set the
OFF. upper/lower limit of each vital alarm.
discontinuity.
The arrhythmia alarm occurs frequently The dominant QRS is not appropriate for Re-learn the patient ECG.
when heart rate is normal. (Only when arrhythmia monitoring.
using the QS-831V upgrade kit.) Patient moved or EMG noise is Change the electrode position to
superimposed. where there is less muscle.
SpO2

SpO2 value is not displayed on the The SpO2 connection cord is Connect the SpO2 connection
screen. disconnected from the SpO2 connector cord to the SpO2 connector of the
of the defibrillator. defibrillator.
The SpO2 probe is disconnected from the Firmly connect the probe to the SpO2
SpO2 connection cord. connection cord.
Cable discontinuity in SpO2 connection Replace the SpO2 connection cord or
cord or probe. probe.
SpO2 probe attachment to the patient is Firmly attach the probe to the
loose. patient.
Dotted lines appear instead of the pulse SpO2 probe attachment to the patient is Firmly attach the probe to the
waveforms. loose. patient.
Faulty SpO2 probe. Replace the SpO2 probe.
Faulty SpO2 connection cord. Replace the SpO2 connection cord.
Faulty SpO2 board. Replace the SpO2 board.
Faulty MP board. Replace the MP board.
Pulse waveform is not displayed on the SpO2 probe is disconnected from the Connect the probe to the SpO2
screen. SpO2 connection cord. connection cord.
SpO2 connection cord is disconnected Connect the SpO2 connection cord to
from the defibrillator. the defibrillator.
Faulty SpO2 probe. Replace the SpO2 probe.
Faulty SpO2 connection cord. Replace the SpO2 connection cord.
Faulty MP board. Replace the MP board.
Unstable SpO2 value. The probe size is inappropriate. Use the correct size probe.
The probe is attached to the same limb Attach the probe to the other limb.
that is used for NIBP or invasive blood
pressure measurement.
An ESU is used. Locate the ESU as far as possible
from the probe and wait until the
pulse wave stabilizes.
Measuring on the venous pulse. Cannot measure correctly.
Probe is damaged. Probe is disinfected by an unspecified Disinfect the probe using the
procedure. specified method or replace the probe
with a new one.
The probe is repeatedly used. Replace the probe with a new one
when it is deteriorated.

2. TROUBLESHOOTING

Sine wave noise on the pulse wave. Light interference. Cover the attachment site with a
blanket.
No sync sound. Sync sound volume settings is small. Increase the volume on the
VOLUME window.
Sync source is set to “ECG” or Set “SYNC SOURCE” to “SpO2”.
“PRESS”.
discontinuity.
CO2

The measured value is not displayed on The CO2 sensor kit cable is disconnected Connect the CO2 sensor kit cable
the screen. from the multi connector of the to the multi connector of the
defibrillator. defibrillator.
CO2 gas is in the inspiration. With the CO2 sensor kit,
measurements are based on the
assumption of no CO2 gas in the
inspiration. Do not connect a Jackson
Rees respiration circuit or Mapleson
D respiration circuit to the patient.
Measurement cannot be done
correctly.
The airway adapter is dirty. Replace the airway adapter with a
new one.
The measurement is performed where Consider the atmospheric pressure
atmospheric pressure is low, such as at when making evaluations.
high altitude.
The measured value is high. N2O is mixed in the inspiration or when Remove the cause and measure
high concentration of oxygen is inspired. again.
The measured value is inaccurate. Jackson Rees respiration circuit or Cannot measure correctly. Do not
Mapleson D respiration circuit is connect a Jackson Rees respiration
connected to the patient. circuit or Mapleson D respiration
circuit to the patient.
The respiration rate of the patient is very Cannot measure correctly.
high.
The respiration is irregular. Cannot measure correctly.
Oscillation Check the respirator and remove the
cause.
Currently doing suction. Do not let the suction catheter in the
airway adapter.
CO2 value does not change. The airway adapter is detached from the Check the airway adapter
patient. attachment.
The patient is in apnea. The previous value is displayed on
the screen until the next inspiration is
detected. Check patient ventilation.
Faulty CO2 sensor kit. Replace the CO2 sensor kit.
The respiration waveform does not Oscillation Check the respirator and remove the
appear. cause.
The CO2 sensor is disconnected from the Connect the CO2 sensor to the
respiration circuit. respiration circuit.
Faulty CO2 sensor kit. Replace the CO2 sensor kit.

2. TROUBLESHOOTING

The red LED on the CO2 adapter blinks. CO2 sensor or CO2 adapter is faulty. Replace the CO2 sensor or CO2
adapter with a new one. 2
The respiration has not been detected for The red LED blinks when the
longer than 20 s. respiration has not been detected for
longer than 20 s regardless of the
alarm setting on the defibrillator.
NIBP

Cuff inflation pressure is less than The cuff hose is not connected to the Connect the cuff hose to the socket
10 mmHg or NIBP data display cuff socket properly. properly.
disappears for a few seconds. The cuff is not wrapped around the arm Wrap the cuff around the upper arm.
or is wrapped too loosely.
The cuff does not inflate when manually The cuff hose is not connected to the Connect the cuff hose to the socket
starting NIBP measurement. cuff socket. firmly.
The cuff hose or air hose may be folded Check the cuff hose and air hose.
or squeezed when the cuff pressure
display on the screen increases quickly
but the actual cuff does not inflate.
Abnormal measurement results are The cuff size is not correct. Select the cuff which fits the patient’s
displayed. limb circumference.
The cuff is not wrapped around the arm Wrap the cuff around the upper arm,
correctly. not too tightly or too loosely.
Body movement. Prevent the patient from moving
during measurement.
Measurement on the wrong site. Measure NIBP at the correct site.
The cuff is suddenly deflated during The NIBP measurement is manually
—
inflation. cancelled during inflation.
Auto measurement does not start even The time interval for the NIBP auto Set the correct time interval.
when the time interval has passed. measurement is set incorrectly.
The cuff suddenly inflates. The measurement mode is set to auto Check the time interval.
mode.
Cannot connect cuff to the air hose. Unspecified cuff is used. Use a cuff specified by Nihon
Kohden.
Cannot measure NIBP. Noise which disables calculation of the Remove the cause.
(There is a “Bong bing” sound and blood pressure has interfered.
measurement does not start.) The air hose is bent or squeezed. Remove the cause.
The cuff has worn out. Use a new cuff.
Blood congestion occurs. Measuring over a long period of time at Increase the measuring interval.
intervals less than 2.5 minutes. Do not measure NIBP over a long
time.
Thrombus occurs. Measuring a patient with known Do not perform NIBP measurement
bleeding disorders or a sickle anemia on such a patient.
patient.
Measured value is displayed in small 10 minutes has passed after Perform NIBP measurement.
characters. measurement. (Measured value is old.)

2. TROUBLESHOOTING
Blood Pressure (PRESS)

The acquired blood pressure value is Air bubbles remain in the circuit. Remove the air bubbles.
different from the estimated value. An extra tube is connected in the circuit. Remove the extra tube.
The position of the blood pressure Check the position of the blood
transducer is inappropriate. pressure transducer.
A blood pressure transducer with Check the blood pressure transducer.
different sensitivities is used.
Other causes. Perform zero balance adjustment
again.
No invasive blood pressure value The measurement is out of range. Check the measuring condition.
appears on the screen. The blood pressure transducer is Replace the blood pressure
damaged. transducer with a new one.
Measured value is not displayed. Calibration is not performed. Perform calibration.
Temperature

The temperature value is not displayed The temperature probe or temperature Replace the temperature probe or
on the screen. connection cord is faulty. temperature connection cord with a
new one.
Faulty TEMP board. Replace the MP board.
Recording

Printing is blurred. Dots are missing. The thermal head is dirty. • Clean the thermal head with Nihon
Kohden specified head cleaning
pen (option). If it does not solve
the problem, the recorder unit is
faulty. Replace the recorder unit.
• Perform the RECORDER TEST
on the SYSTEM SETUP screen to
check the print function.
Nihon Kohden specified paper is not Use Nihon Kohden specified
used. recording paper.
Recording paper cannot be set correctly. Nihon Kohden specified paper is not Use Nihon Kohden specified
used. recording paper.
Nothing is printed. The recording paper is not loaded. Load recording paper.
Recorder door is not properly closed. Close the door until it clicks.
The recording paper is set with the Set the recording paper correctly.
wrong side facing up.
Faulty REC/EXT board. Replace the REC/EXT board.
Faulty recorder unit. Replace the recorder unit.
Paper skews to one side. The recording paper is not loaded Set the paper straight.
correctly.
Printout is faint. The recorder unit temperature is too hot. Put the defibrillator in a cooler place.
If this does not solve the problem,
the recorder unit or CONTROL
board is faulty. Replace the recorder
unit or CONTROL board.

2. TROUBLESHOOTING
Battery
Problem Possible Cause Action 2

The battery charging lamp or battery The battery temperature is out of Place the defibrillator in the place at
charging completion lamp is blinking. specified range. the specified range.
After starting battery charging, the Faulty battery pack. Replace the battery pack with a new
charging stops. (Neither battery charging one.
lamp nor battery charging completion When battery pack replacement does Replace the POWER board.
lamp lights.) not solve the problem, POWER board is
faulty.
The “REPLACE BATTERY” message The battery pack is deteriorated. Replace the battery pack with a new
appears. one.
SD Card

Data cannot be saved in the SD card. Upgrade kit is inserted instead of an SD Insert a card for storage.
card.
The card is not inserted. Insert a specified card.
The card is not inserted properly. Properly insert the card.
A card other than specified card is Insert a specified card.
inserted.
Memory is full. Use a new card or delete unnecessary
data.
The card is write-protected. Remove the write-protect.
The card is not formatted. Format the card in the SYSTEM
SETUP screen.
The SD card was removed while the Turn the control dial to the OFF
defibrillator power was on and the position to turn the defibrillator off
defibrillator was affected by static then turn the defibrillator on again.
electricity.

Section 3 Disassembly
3
Before You Begin.................................................................................................................................................. 3.3

Warnings, Cautions and Notes................................................................................................................... 3.3
Registering Serial Number after Board Replacement................................................................................ 3.4
Required Tools............................................................................................................................................ 3.5
Connection Diagram............................................................................................................................................. 3.6
Removing the External Paddle Holder or Top Cover.......................................................................................... 3.11
Removing the Optional 12 Lead ECG Unit......................................................................................................... 3.14
Removing the QI-831V AUXOUT Unit and QI-832V Bluetooth® Module............................................................ 3.16
Removing the Front Case................................................................................................................................... 3.19
Removing the LCD Unit and the LED DRIVER Board........................................................................................ 3.21
Removing the UR-0414 CONTROL Board and the UR-0415 ECG/PACER Board............................................ 3.23
Removing the HV-831V HV Unit and UR-0418 HV CPU Board......................................................................... 3.26
Note for Assembling the Defibrillator after HV Unit Replacement............................................................ 3.27
Removing the MP Unit........................................................................................................................................ 3.29
Removing the Input Enclosure................................................................................................................. 3.30
Removing the UR-0454 TEMP Board...................................................................................................... 3.31
Removing the UR-0455 MP Board........................................................................................................... 3.32
Removing the UR-3908 SpO2 Board........................................................................................................ 3.33
Removing the UR-0444 ECG CONN1 Board........................................................................................... 3.33
Removing the UR-0445 ECG CONN2 Board........................................................................................... 3.34
Removing the NIBP Pump....................................................................................................................... 3.34
Removing the Valve.................................................................................................................................. 3.35
Removing the UR-0431 REC/EXT Board........................................................................................................... 3.36
Removing the Recorder Unit.............................................................................................................................. 3.37
Removing the UR-0417 Power Board................................................................................................................ 3.39
Removing the KEY/LED Boards......................................................................................................................... 3.42
Removing the Speaker....................................................................................................................................... 3.44
Removing the Paddle Connector........................................................................................................................ 3.45

3. DISASSEMBLY
The procedures in this section explain how to remove, replace and install major
components in the defibrillator.

3. DISASSEMBLY
Before You Begin
Warnings, Cautions and Notes 3
WARNING WARNING
The HV capacitor can store lethal amounts of Removal and replacement of any components in
energy. Discharge this capacitor before touching the defibrillator should only be done by qualified
any high voltage component (HV capacitor, service personnel.
biphasic HV unit, paddle socket or paddles).
WARNING
To avoid the possibility of injury to yourself or
damage to the defibrillator, do not install or
remove any component while the power is on.
When disassembling, make sure that the
defibrillator is off, the AC power cord is
disconnected from the defibrillator and the battery
pack is removed from the defibrillator. There are
several high voltage units inside the defibrillator:
LCD backlight, high voltage capacitor, pacing DC/
DC converter and switching regulator.
CAUTION CAUTION
To avoid accidental discharge of static electricity Fuses on the main board and AC/DC unit cut off
which could damage the components of the the power when an abnormality occurs in the
defibrillator, use a grounded wrist strap when defibrillator. Eliminate the malfunction before
installing or removing any component of the replacing the fuse. Use the correct fuse only.
defibrillator.
CAUTION
Use only parts recommended by Nihon Kohden
to assure maximum performance from your
defibrillator.

3. DISASSEMBLY
NOTE
When the ECG/PACER board, CONTROL board or biphasic HV unit is
replaced with a new one, do the following adjustment. Refer to “System
Maintenance Screen – Adjust AD Screen” in Section 4.
ECG/PACER board:
• ECG sensitivity and offset
• Battery voltage and battery current settings
• Paddle contact impedance threshold
Control board:
• ECG sensitivity and offset
• Charge energy, charge time, delivered energy and TTR
• Battery voltage setting
Biphasic HV unit:
• Charge energy, charge time, delivered energy and TTR
Registering Serial Number after Board Replacement

After replacing the UR-0414 CONTROL board, register the serial number of the
board by the following procedure.
1. While pressing and holding the Silence Alarms key, turn the control dial to
the BASIC CHECK position to display the SYSTEM SETUP screen.
2. Select SYSTEM SETUP with the ITEM ↑ or ITEM ↓ function key and press
the OK function key.
3. Select ID with the ↑ or ↓ function key and enter the serial number with
SELECT ↑ or SELECT ↓ function key.
4. Saving the settings using the procedure described in “Saving the Settings
before Maintenance (Flash Save Procedure)” in Section 4.
5. Turn the control dial to the BASIC CHECK position and confirm the serial
number on the BASIC CHECK screen.
If the serial number is incorrect, clear the settings on the System

Maintenance screen and register the serial number again. To clear the
settings, refer to “Changing the Settings to Factory Default” in Section 5.

3. DISASSEMBLY
Required Tools
• Anti-static bench mat
• Wrist ground strap
• Screwdriver (insulated type, for M2.6 and M3 screws)
3
• Hex socket driver (for 3 mm spacer bolt and nut)
• Tweezers

3.6
TEC-8321 Block Diagram
CN101 CN601
TEC-8321
CN602
CN0101 MP SPEAKER
CN202
SpO2 UR-04301 KEY/LED1
CN603
CN0501
CN105
CN104
3. DISASSEMBLY
UR-3908
CN701 KEY/LED2 MIC
CN201
UR-04161
CN
LCD ROTARY SW
ALARM
CNA102
CNA102
CNA301
CNA301
CN
Indicator
CN1206
STATUS
CN101
CN1202
CNA203
CNA203
Indicator
Connection Diagram
CONTROL AUXOUT
CNA105A
BATT1
CN101
CN107
CN102
CN101
CN
CN0702
UR-0426
CN101
CNA105B UR-0414
CN0201
CN109
BATT-CONN
CNA104A
CNA104B
POWER BLUETOOTH
CN1
CN106
UR-0417 UR-0427
BATT2 SD CARD
CN110
CN0701
CNA107B
CNA106A
CNA106B
AC/DC REC/EXT
CN
CN1204
CN102
UR-0431
BATT-CONN
CNA107A
CN1203
CN1201 CN1205
CN1501 CN1506
CN1504
CN1505
CN104
RECORDER
THERMHEAD
WS-831V
MOTOR ASSY
CN1001
CN102
CN1502
CN105
MOTOR
ECG/PACER UR-0419
HV CPU UR-04151
CN1002
UR-0418
CN101
12L-ECG
CN201
PADDLE-CONN UR-0428
CN401
CN101
CN
CN101
CN102
CN1503
LEAD-ECG FLOATING AREA
CN202
CN103
HV SW ECG-CONN
CN
ECG-CONN2
CN103
CN201
CNA203
CNA201
CN0701
CN0101
UR-0429
HV FL CN102
BIPHASIC HV UNIT
HV-831V
Service Manual TEC-8300

CN102 CN101 CN601
CN602
TEC-8322
CN0101 MP SPEAKER
TEMP
CN202
CN303
CN302
CN301
CN603
CN0501
CN105
CN104
UR-3908
CN701 KEY/LED2 MIC
CN201
UR-04161
CN
LCD ROTARY SW
ALARM
CNA102
CNA102

CNA301
CNA301
CN
Indicator
CN1206
STATUS
CN101
CN1202
CNA203
CNA203
Indicator
CONTROL AUXOUT
CNA105A
BATT1
CN101
CN107
CN102
CN101
CN
CN0702
UR-0426
CN101
CNA105B UR-0414
CN0201
CN109
BATT-CONN
CNA104A
CNA104B
POWER BLUETOOTH
CN1
CN106
UR-0417 UR-0427
BATT2 SD CARD
CN110
CN0701
CNA107B
CNA106A
CNA106B
AC/DC REC/EXT
CN
CN1204
CN102
UR-0431
BATT-CONN
CNA107A
CN1203
CN1201 CN1205
CN1501 CN1506
CN1504
CN1505
CN104
RECORDER
THERMHEAD
WS-831V
MOTOR ASSY
CN1001
CN102
CN1502
CN105
MOTOR
ECG/PACER UR-0419
HV CPU UR-04151
CN1002
UR-0418
CN101
12L-ECG
CN201
PADDLE-CONN UR-0428
CN401
CN101
CN
CN101
CN102
CN1503

CN202
CN103
HV SW ECG-CONN
CN
ECG-CONN2
CN103
CN201
CNA203
CNA201
CN0701
CN0101
UR-0429
HV FL CN102
BIPHASIC HV UNIT
HV-831V
3.7
3. DISASSEMBLY
3
3.8
CN102 CN101 CN601 KEY
CNA103
CN602
TEC-8332
CNA103
CN0101 MP SPEAKER
TEMP
CN202
CN303
CN302
CN301
CN603
CN0501
CN105
CN104
UR-3908
3. DISASSEMBLY
CN701 KEY/LED2 MIC
CN201
UR-0416
CN
LCD ROTARY SW
ALARM
CNA102
CNA102
CNA301
CNA301
CN
Indicator
CN1206
STATUS
CN101
CN1202
CNA203
CNA203
Indicator
CONTROL AUXOUT
CNA105A
BATT1
CN101
CN107
CN102
CN101
CN
CN0702
UR-0426
CN101
CNA105B UR-0414
CN0201
CN109
BATT-CONN
CNA104A
CNA104B
POWER BLUETOOTH
CN1
CN106
UR-0417 UR-0427
BATT2 SD CARD
CN110
CN0701
CNA107B
CNA106A
CNA106B
AC/DC REC/EXT
CN
CN1204
CN102
UR-0431
BATT-CONN
CNA107A
CN1203
CN1201 CN1205
CN1501 CN1506
CN1504
CN1505
CN104
RECORDER
THERMHEAD
WS-831V
MOTOR ASSY
CN1001
CN102
CN1502
CN105
MOTOR
ECG/PACER UR-0419
HV CPU UR-0415
CN1002
UR-0418
CN101
12L-ECG
CN201
PADDLE-CONN UR-0428
CN401
CN101
CN
CN101
CN102
CN1503
CN202
CN103
HV SW ECG-CONN
CN
ECG-CONN2
CN103
CN201
CNA203
CNA201
CN0701
CN0101
UR-0429
HV FL CN102
BIPHASIC HV UNIT
HV-831V

CN801 CN102 CN101 CN601
CN602
TEC-8342
CN0101 MP SPEAKER
TEMP
CN202
CN303
CN302
CN301
CN603
CN0501
CN105
CN104
UR-3908
CN701 KEY/LED2 MIC
CN201
UR-04161
CN
LCD ROTARY SW
ALARM
CNA102
CNA102

CNA301
CNA301
CN
Indicator
CN1206
STATUS
CN101
CN1202
CNA203
CNA203
Indicator
CONTROL AUXOUT
CNA105A
BATT1
CN101
CN107
CN102
CN101
CN
CN0702
UR-0426
CN101
CNA105B UR-0414
CN0201
CN109
BATT-CONN
CNA104A
CNA104B
POWER BLUETOOTH
CN1
CN106
UR-0417 UR-0427
BATT2 SD CARD
CN110
CN0701
CNA107B
CNA106A
CNA106B
AC/DC REC/EXT
CN
CN1204
CN102
UR-0431
BATT-CONN
CNA107A
CN1203
CN1201 CN1205
CN1501 CN1506
CN1504
CN1505
CN104
RECORDER
THERMHEAD
WS-831V
MOTOR ASSY
CN1001
CN102
CN1502
CN105
MOTOR
ECG/PACER UR-0419
HV CPU UR-04151
CN1002
UR-0418
CN101
12L-ECG
CN201
PADDLE-CONN UR-0428
CN401
CN101
CN
CN101
CN102
CN1503

CN202
CN103
HV SW ECG-CONN
CN
ECG-CONN2
CN103
CN201
CNA203
CNA201
CN0701
CN0101
UR-0429
HV FL CN102
BIPHASIC HV UNIT
HV-831V
3.9
3. DISASSEMBLY
3
3.10
CN801 CN102 CN101 CN601 KEY
CNA103
CN602
TEC-8352
CNA103
CN0101 MP SPEAKER
TEMP
CN202
CN303
CN302
CN301
CN603
CN0501
CN105
CN104
UR-3908
3. DISASSEMBLY
CN701 KEY/LED2 MIC
CN201
UR-0416
CN
LCD ROTARY SW
ALARM
CNA102
CNA102
CNA301
CNA301
CN
Indicator
CN1206
STATUS
CN101
CN1202
CNA203
CNA203
Indicator
CONTROL AUXOUT
CNA105A
BATT1
CN101
CN107
CN102
CN101
CN
CN0702
UR-0426
CN101
CNA105B UR-0414
CN0201
CN109
BATT-CONN
CNA104A
CNA104B
POWER BLUETOOTH
CN1
CN106
UR-0417 UR-0427
BATT2 SD CARD
CN110
CN0701
CNA107B
CNA106A
CNA106B
AC/DC REC/EXT
CN
CN1204
CN102
UR-0431
BATT-CONN
CNA107A
CN1203
CN1201 CN1205
CN1501 CN1506
CN1504
CN1505
CN104
RECORDER
THERMHEAD
WS-831V
MOTOR ASSY
CN1001
CN102
CN1502
CN105
MOTOR
ECG/PACER UR-0419
HV CPU UR-0415
CN1002
UR-0418
CN101
12L-ECG
CN201
PADDLE-CONN UR-0428
CN401
CN101
CN
CN101
CN102
CN1503
CN202
CN103
HV SW ECG-CONN
CN
ECG-CONN2
CN103
CN201
CNA203
CNA201
CN0701
CN0101
UR-0429
HV FL CN102
BIPHASIC HV UNIT
HV-831V

3. DISASSEMBLY
Removing the External Paddle Holder or Top Cover
When using the optional DP-831VK external paddle holder 3

1. Remove the six BH 3 × 8 screws from the holder and remove the holder.
Rear panel BH 3 × 8 screw
External paddle
holder
Left side panel Right side panel

TEMP CAP* BH 3 × 8 screw BH 3 × 8 screw

3. DISASSEMBLY
* The TEMP CAP is removed when the holder is removed. Be careful not to
lose the cap.
TEMP CAP
2. Turn the external paddle holder upside down.
3. Remove the two P-type 3 × 8 screws, two hexagonal nuts and remove the
UR-0315 test load.
P-type 3 × 8 screws
UR-0315 test load
Hexagonal nuts

3. DISASSEMBLY
When using the standard top cover

Remove the six BH 3×8 screws from the top cover and remove the top cover.
Rear panel BH 3 × 8 screw
Top cover
Left side panel Right side panel

TEMP CAP* BH 3 × 8 screw BH 3 × 8 screw
* The TEMP CAP is removed when the cover is removed. Be careful not to
lose the cap.
TEMP CAP

3. DISASSEMBLY
Removing the Optional 12 Lead ECG Unit
When the 12 lead ECG unit is not mounted on the defibrillator, skip this
procedure.
Before removing the option board and mounted module, remove the defibrillator
top cover or the optional DP-831VK external paddle holder. Refer to “Removing
the External Paddle Holder or Top Cover” in this section.
1. Remove the two PS 3 × 8 screws which secures the 12 lead ECG unit to the
defibrillator.
2. Disconnect the connector of the 12 lead ECG unit cable.

Disconnect this connector before
removing the 12 lead ECG unit. AC-831V 12 lead ECG unit
PS 3 × 8 screws

3. DISASSEMBLY
3. Remove the 12 lead ECG unit from the defibrillator by sliding the unit
upward.

3. DISASSEMBLY
Removing the QI-831V AUXOUT Unit and QI-832V Bluetooth®

Module
Before removing the optional unit and mounted module, remove the defibrillator
top cover or the optional DP-831VK external paddle holder. Refer to “Removing
the External Paddle Holder or Top Cover” in this section.
1. Remove the BH 3 × 14 screw from the optional unit (QI-831V AUXOUT
unit).
BH 3 × 14 screw
Optional
unit
2. Remove the option unit and remove the cable* from the defibrillator.
Remove these connectors. The number of connectors

depending on the installed optional units.
* When the optional QI-832V Bluetooth® module is mounted, remove two

cables from the defibrillator.

3. DISASSEMBLY
When removing the optional unit, be careful not to pull the cables between
the unit and the defibrillator.
3. When mounting the optional QI-832V Bluetooth® module, remove the

Bluetooth® module from the optional unit. If not, skip this step. 3
i) Remove the BH 3 × 8 screw on the board side of the optional unit.
BH 3 × 8 screw
ii) Turn the optional unit and remove two BH 3 × 8 screws which secures
the QI-832V Bluetooth® module to the optional unit and remove the
QI-832V Bluetooth® module from the optional unit.
BH 3 × 8 screws
QI-832V
Bluetooth®
module

3. DISASSEMBLY
4. When using the QI-831V AUXOUT unit, remove the UR-0426 AUXOUT
board from the unit. If not, skip this step.
Remove the PS 3 × 8 screw and hexagonal bolt from the UR-0426
AUXOUT board and remove the board from the unit. When removing the
AUXOUT board, connector part is removed from the AUXOUT unit. Be
careful not to lose the part.
UR-0426 AUXOUT board
When removing the

AUXOUT unit board,
be careful not to lose
this part.
PS 3 × 8 screw Hexagonal bolt

3. DISASSEMBLY
Removing the Front Case
Before removing the front case, remove the defibrillator top cover (or the 3
optional DP-831VK external paddle holder). Refer to “Removing the External
Paddle Holder or Top Cover” in this section.
1. Remove the fourteen BH 3 × 8 screws from the defibrillator rear panel and
remove the front case from the defibrillator.
Rear BH 3 × 8 screw
Bottom
Top

3. DISASSEMBLY
Right side panel Left side panel
2. Disconnect the two paddle connectors and FFC connector of the keys on the
front panel. Open the front panel carefully so that the connected cables are
not pulled or damaged.

3. DISASSEMBLY
Removing the LCD Unit and the LED DRIVER Board
Before removing the LCD unit and the LED DRIVER board, remove the 3
following.
• Defibrillator top cover (or the optional DP-831VK external paddle holder)
• Front case
For removing these, refer to the corresponding procedures earlier in this section.
1. Remove the four PS 2.6 × 8 screws and two connectors which secures the
LCD to the front panel of the defibrillator and remove the LCD from the
defibrillator.
LCD
Connector
Connector
PS 2.6 × 8 screws

3. DISASSEMBLY
2. Remove the two PS 3 × 8 screws and a connector from the LED DRIVER
board and remove the LED DRIVER board.
LED DRIVER board
Connector

3. DISASSEMBLY
Removing the UR-0414 CONTROL Board and the UR-0415

ECG/PACER Board
3
Before removing the CONTROL board and ECG/PACER board, remove the
following.
• Front case
• LCD unit and LED DRIVER board
1. Remove the eight PS 3 × 8 screws which secure the UR-0414 CONTROL
board and the UR-0415 ECG/PACER board, three connectors on the
UR-0414 CONTROL board and four connectors on the UR-0415 ECG/
PACER board.
ECG/PACER board connector
ECG/PACER board
CONTROL board
connector
: PS 3 × 8 screws
Metal plate Control board
2. Remove the UR-0414 CONTROL board and the UR-0415 ECG/PACER

board with the metal plate from the defibrillator.

3. DISASSEMBLY
3. Remove the two connectors on the UR-0415 ECG/PACER board. Be careful

not to pull or damage the cables connected to the boards.
Connectors
ECG/PACER board
4. Remove the eight PS 3 × 8 screws and a connector which secure the
UR-0415 ECG/PACER board and remove the UR-0415 ECG/PACER board.
PS 3 × 8 screw Connector
ECG/PACER board

3. DISASSEMBLY
5. Remove the insulation sheet and remove the eight hexagonal bolts and one
PS 3 × 8 screw which secure the metal board and remove the metal board
from the UR-0414 CONTROL board.
PS 3 × 8 screw
Hexagonal bolt Insulation sheet

3. DISASSEMBLY
Removing the HV-831V HV Unit and UR-0418 HV CPU Board
Before removing the HV unit, remove the followings.

• Front case
• UR-0414 CONTROL board and UR-0415 ECG/PACER board with metal
board
NOTE
Before removing the HV-831V HV unit, order a hook blank panel (6124-
906138).
1. Remove the two PS 3 × 8 screws on the front side.
HV CPU board
HV unit
PS 3 × 8
screw

3. DISASSEMBLY
2. Peel off the blank label on the rear panel and remove the four BH 3 × 8
screws and remove the HV-831V HV unit from the defibrillator.
Peel the blank panel off.
BH 3 × 8 screw
NOTE
When assembling the defibrillator, make sure to attach the hook blank
panel to the rear cover so that the four BH 3 × 8 screws are covered.
Note for Assembling the Defibrillator after HV Unit Replacement

The HV unit cable is affixed to the HV unit at the factory. This tape is for
preventing the cable from catching on a screw or other object inside the
defibrillator.
Do not remove this tape.

3. DISASSEMBLY
When attaching the screw shown in the picture, be careful not to pinch the cable
under the screw.

3. DISASSEMBLY
Removing the MP Unit
Before removing the MP unit, remove the followings. 3

• Front case
• LCD unit and the LED DRIVER board
board
• HV-831V HV unit
Remove the six BH 3 × 8 screws which secure the MP unit and remove the MP
unit from the defibrillator.
BH 3 × 8 screw
MP unit
When removing the MP unit, pull the unit slightly to the right so that the TEMP
modular jack does not catch on the input enclosure.
TEMP modular jack

3. DISASSEMBLY
Removing the Input Enclosure

1. Remove the connector of the TEMP board.
TEMP board
2. Remove the five BH 3 × 8 screws and remove the input enclosure from the
unit.
Input enclosure

3. DISASSEMBLY
Removing the UR-0454 TEMP Board

1. Remove the two PS 3 × 8 screws and remove the TEMP board from the
input enclosure.
3
2. Remove the PS 3 × 8 screw which secures the metal plate to the TEMP
board and remove the metal plate from the TEMP board.
TEMP board
Metal plate
PS 3 × 8 screw

3. DISASSEMBLY
Removing the UR-0455 MP Board

1. Remove the L-shaped joint which is connected to the pump tube and two
connectors on the rear side on the MP board.
L-shaped joint
Connectors MP board
2. Remove the eight PS 3 × 8 screws which secure the UR-0455 MP board and
remove the MP board from the unit.
MP board

3. DISASSEMBLY
Removing the UR-3908 SpO2 Board

Remove the four PS 3 × 6 screws which secure the UR-3908 SpO2 board and
remove the UR-3908 SpO2 board from the UR-0430 MP board.
3
PS 3 × 6
screws
SpO2 board
Removing the UR-0444 ECG CONN1 Board

Remove the three PS 3 × 8 screws and connector which secure the metal board
and UR-0444 ECG CONN1 board and remove the metal board and UR-0444
ECG CONN1 board from the unit.
Connector
ECG CONN 1
board
One PS 3 × 8 screw

is on this side.

3. DISASSEMBLY
Removing the UR-0445 ECG CONN2 Board

1. Remove the two PS 3 × 8 screws which secure the UR-0445 ECG CONN2
board to the unit and remove the UR-0445 ECG CONN2 board from the
unit.
2. Remove the PS 3 × 8 screw from the metal board on the UR-0445 ECG
CONN2 board and remove the metal panel from the ECG CONN2 board.
ECG CONN2
board
PS 3 × 8 screw
Removing the NIBP Pump

Remove the two PS 3 × 8 screws, disconnect the pump tube from the unit and
remove the pump from the unit.
PS 3 × 8 screw
PS 3 × 8 screw
is on this side.
Disconnect the tube.

3. DISASSEMBLY
Removing the Valve

1. Remove four PS 2 × 4 screws which secure the valve, remove the two PS
3 × 8 screws which secure the valve holder and remove the valve holder
from the unit.
3
2. Disconnect the two tubes connected to the valve and remove the valve from
the unit.
Remove these tubes from the valve.
PS 3 × 8 screw PS 3 × 8 screw
PS 2 × 4 screws Valve holder

3. DISASSEMBLY
Removing the UR-0431 REC/EXT Board
Before removing the REC/EXT board, remove the following.

• Front case
board
Remove the four PS 3 × 8 screws and two connectors on the UR-0431 REC/EXT
board and remove the UR-0431 REC/EXT board from the defibrillator.
REC/EXT board
Connectors
PS 3 × 8 screw

3. DISASSEMBLY
Removing the Recorder Unit
Before removing the recorder unit, remove the following. 3

• Front case
board
• HV-831V HV unit
• UR-0431 REC/EXT board
NOTE
Before removing the recorder unit, order a rubber sponge (sponge 46 ×
25 × 3, 6114-906977A).
1. Remove the three PS 3 × 8 screws.

Let this cable slide through
the rubber sponge when
removing the recorder unit.
Replace this rubber

sponge after replacing
the recorder unit.
PS 3 × 8 screw WS-831V recorder unit

3. DISASSEMBLY
2. Remove the WS-831V recorder unit from the defibrillator by sliding the unit
towards the right side of the defibrillator.
NOTE
After replacing the recorder unit, replace the rubber sponge. Using old
rubber sponge decreases water-proof performance.

3. DISASSEMBLY
Removing the UR-0417 Power Board
Before removing UR-0417 power board, remove the followings. 3

• Front case
board
• HV-831V unit
• MP unit
• UR-0431 REC/EXT board
1. Remove the two PS 3 × 8 screws on the front side which secure the metal
plates to the rear panel.
Metal plates
PS 3 × 8 screw

3. DISASSEMBLY
2. Remove the two BH 3 × 10 screws on the defibrillator bottom.
3. Remove the two metal plates from the defibrillator.

3. DISASSEMBLY
4. Remove the two BH 3 × 8 screws which secure the insulation sheet to the
defibrillator and remove the insulation sheet.
Insulation sheet
BH 3 × 8 screw
5. Remove the six BH 3 × 8 screws which secure the UR-0417 POWER board
to the defibrillator and remove the UR-0417 POWER board.
BH 3 × 8 screw
POWER board

3. DISASSEMBLY
Removing the KEY/LED Boards
Before removing the KEY/LED board, remove the followings.

• Front case
1. Remove the control dial by pulling it.
2. Remove a hexagonal nut, a washer and O-shaped ring of the control dial.
Hexagonal nut

3. DISASSEMBLY
3. Turn the front panel and remove the four P-type 3 × 8 screws, two PS 3 × 8
screws and FFC connector and remove the UR-0452 KEY/LED board from
the defibrillator.
PS 3 × 8 3
screws
P-type 3 × 8
screws
KEY/LED
board
Disconnect this
connector.
4. Remove the nine P-type 3 × 8 screws and a connector to remove the
UR-0453 KEY/LED board from the defibrillator.
P-type 3 × 8 screw
KEY/LED board Disconnect this connector.

3. DISASSEMBLY
Removing the Speaker
Before removing the speaker, remove the followings.

• Front case
Remove the two P-type 3 × 8 screws and remove the speaker.
Speaker
P-type 3 × 8 screws

3. DISASSEMBLY
Removing the Paddle Connector
Before removing the paddle connector, remove the followings. 3

• Front case
Remove the four P-type 3 × 8 screws and remove the paddle connector.
Paddle connector P-type 3 × 8 screw

Section 4 Maintenance
General................................................................................................................................................................. 4.4 4
Periodic Inspection..................................................................................................................................... 4.4
Daily Inspection................................................................................................................................ 4.4
Monthly Inspection........................................................................................................................... 4.4
Yearly Inspection.............................................................................................................................. 4.4
Repair Parts Availability Policy................................................................................................................... 4.4
Before Check........................................................................................................................................................ 4.5
Recording and Saving the Reports............................................................................................................ 4.5
When Using a Loaner Defibrillator............................................................................................................. 4.5
Copying the Settings to the Loaner Defibrillator............................................................................... 4.5
Checking the Appearance.................................................................................................................................... 4.6
Checking the SB-831V Battery Pack.................................................................................................................... 4.7
Checking the Defibrillator..................................................................................................................................... 4.8
Connecting the Checker and Turning the Defibrillator On.......................................................................... 4.8
Adjusting the Sync Sound.......................................................................................................................... 4.9
Checking the Recorder............................................................................................................................... 4.9
Record/Stop Key.............................................................................................................................. 4.9
Date and Time Printed on the Recording Paper.............................................................................. 4.9
Event Key......................................................................................................................................... 4.9
Recording Quality............................................................................................................................. 4.9
Detecting Out of Paper................................................................................................................... 4.10
Checking the Defibrillation Function in Manual Mode........................................................................................ 4.11
Checking the Connector Off Detection..................................................................................................... 4.11
Checking the Duration of Charging Energy.............................................................................................. 4.13
AC Power....................................................................................................................................... 4.13
Battery Power................................................................................................................................. 4.14
Checking the Discharged Waveform........................................................................................................ 4.15
Checking the Discharged Energy............................................................................................................. 4.19
AC Power....................................................................................................................................... 4.20
Battery Power................................................................................................................................. 4.20
Checking the Discharge for When Using the Disposable Pads................................................................ 4.21
Checking the Discharge for When Using the Internal Paddles................................................................. 4.22
Checking for Changing the Energy Setting After Charging is Complete.................................................. 4.22
Checking Internal Discharge.................................................................................................................... 4.23
Checking the Synchronized Cardioversion......................................................................................................... 4.25
Checking the Synchronized Cardioversion Using the Paddle Lead......................................................... 4.25
Checking the Synchronized Cardioversion Using the ECG Lead............................................................. 4.27
Checking in the AED Mode................................................................................................................................ 4.30
Preparation............................................................................................................................................... 4.30
Checking ECG Analysis in AED Mode, Charge and Discharge............................................................... 4.30
Checking the Display................................................................................................................................ 4.32
Checking the Voice Instruction................................................................................................................. 4.32
Checking the Pacing Function............................................................................................................................ 4.33
Preparation............................................................................................................................................... 4.33

Checking the Pacing in Fixed Mode......................................................................................................... 4.34
Checking the Pacing in Demand Mode.................................................................................................... 4.35
Checking the Pacing Rate and Output Current........................................................................................ 4.37
Checking the Monitoring Parameters................................................................................................................. 4.38
Checking the Electrocardiogram (ECG)................................................................................................... 4.38
Preparations................................................................................................................................... 4.38
Checking the Accuracy of the Heart Rate and the Generation of Synchronous Sound................. 4.39
Checking the Sensitivity of ECG.................................................................................................... 4.39
Checking the Detection of the Heart Rate and Electrode-Off Alarms............................................ 4.40
Checking the IBP...................................................................................................................................... 4.41
Preparation..................................................................................................................................... 4.41
Checking the Accuracy of Zero Calibration.................................................................................... 4.41
Checking the Accuracy of the Blood Pressure Value..................................................................... 4.42
Checking the Detection of an Connector-Off Alarm....................................................................... 4.43
Checking the CO2 Value........................................................................................................................... 4.43
Preparation..................................................................................................................................... 4.43
Checking the Accuracy of the Respiration Rate and the CO2 Value.............................................. 4.43
Checking the Detection of an Connector-Off Alarm....................................................................... 4.44
Checking the Measurement Accuracy of the CO2 Sensor Kit........................................................ 4.44
Preparations................................................................................................................................... 4.44
Checking the SpO2 Value......................................................................................................................... 4.49
Preparation..................................................................................................................................... 4.49
Checking the Accuracy of the SpO2 Value and the Pulse Rate...................................................... 4.50
Checking the Detection of Alarm for the SpO2 Value and a Connector-Off Alarm......................... 4.50
Checking the NIBP (TEC-8342/8352 Only).............................................................................................. 4.51
Preparation..................................................................................................................................... 4.51
Checking the Type of the Connected Cuff...................................................................................... 4.51
Checking the Measurement Operation and Display of Measured Value........................................ 4.51
Checking the Measurement Stop Function.................................................................................... 4.51
Checking the Temperature....................................................................................................................... 4.52
Preparations................................................................................................................................... 4.52
Check the Accuracy of Temperature.............................................................................................. 4.53
Checking the Connector-Off Detection.......................................................................................... 4.53
Checking the Sensor-Off Detection................................................................................................ 4.53
Checking the AC-831V 12 Lead ECG Unit......................................................................................................... 4.54
Preparations............................................................................................................................................. 4.54
Checking the 12 Lead ECG Display......................................................................................................... 4.55
Checking the Connector-Off Detection.......................................................................................... 4.55
Safety Check...................................................................................................................................................... 4.56
External Paddles and Internal Paddles.................................................................................................... 4.58
Pad Adapter............................................................................................................................................. 4.58
ECG (Electrode Lead).............................................................................................................................. 4.58
SpO2 Probe.............................................................................................................................................. 4.58
Checking the SB-801V Battery Charger............................................................................................................. 4.59
Inspection Items....................................................................................................................................... 4.59
Safety Check............................................................................................................................................ 4.60
System Maintenance Screen.............................................................................................................................. 4.61
Displaying the System Maintenance Screen............................................................................................ 4.61
Saving the Settings before Maintenance (Flash Save Procedure)........................................................... 4.62

Changing the Settings to Factory Default................................................................................................. 4.63
About the Menu Items.............................................................................................................................. 4.64
System Maintenance Screen Flowchart........................................................................................ 4.64
Default Settings.............................................................................................................................. 4.65
Configuration Screen................................................................................................................................ 4.66
Adjust AD Screen..................................................................................................................................... 4.67
Adjust ECG A/D Screen................................................................................................................. 4.68 4
Adjust HV AD Screen..................................................................................................................... 4.71
Adjust Battery AD Screen.............................................................................................................. 4.74
Paddle Contact A/D Screen........................................................................................................... 4.76
Check Hardware Screen.......................................................................................................................... 4.77
Check Key Screen.......................................................................................................................... 4.77
Check LED Screen......................................................................................................................... 4.79
Check LCD Screen........................................................................................................................ 4.80
Check Buzzer Screen.................................................................................................................... 4.80
Check Voice Screen....................................................................................................................... 4.81
Check Recorder Screen................................................................................................................. 4.83
Check ECG Frequency Screen...................................................................................................... 4.83
Check NIBP Screen....................................................................................................................... 4.84
Check 12 Lead Screen................................................................................................................... 4.91
Examination Screen....................................................................................................................... 4.92
Check Time Constant Screen........................................................................................................ 4.92
Check MP Screen.......................................................................................................................... 4.93
Operation Time Screen............................................................................................................................ 4.93
Version Up Screen................................................................................................................................... 4.94
Debug Mode Screen................................................................................................................................ 4.95
Check String Screen...................................................................................................................... 4.95
AD Viewer Screen.................................................................................................................................... 4.96
Saving the System Maintenance Screens as Bitmap Files................................................................................ 4.97
Maintenance Check Sheet................................................................................................................................. 4.98

4. MAINTENANCE
General
Periodic Inspection
CAUTION
Before maintenance, cleaning or disinfection, turn the defibrillator
power off and remove the AC/DC module and the battery packs from
the defibrillator. Failure to follow this instruction may result in
electrical shock and defibrillator malfunction.
Daily Inspection
Perform the Basic Checks every day. Refer to “Basic Checks” in Section 2 and
“Cleaning, Disinfecting and Sterilizing” in Section 9 of the Operator’s Manual
Part I.
Monthly Inspection
Perform the following tests and checking once a month.
• Battery calibration
• Recorder test
• Defibrillation check (manual and synchronized cardioversion)
• AED function
• Pacing function (TEC-8332/8352)
Check the recorder thermal head and clean the recorder roller every 6 months.
Yearly Inspection
Use the Maintenance Check Sheet at the end of this section.
If the periodic inspection is not performed, degradation or loss of function may

go unnoticed and lead to misdiagnosis.
Service personnel should perform the periodic inspection at least once

every year. Make sure that the defibrillator operates properly and replace the
consumables.
If you found abnormalities as a result of inspection and the defibrillator is

suspected to be faulty, attach an “Unusable” or “Repair request” label to the
defibrillator and contact your Nihon Kohden representative.
Repair Parts Availability Policy

Nihon Kohden Corporation (NKC) shall stock repair parts (parts necessary to
maintain the performance of the instrument) for a period of 8 years from the
date of delivery. In that period NKC or its authorized agents will repair the
instrument. This period may be shorter than 8 years if the board or part necessary
for the faulty section is not available.

4. MAINTENANCE
Before Check
Recording and Saving the Reports

The data in the internal memory may be lost while checking. Before check,
record the data in the internal memory or save the data in the internal memory to 4
an SD card.
For recording and saving the data in an SD card, refer to the Operator’s Manual
Part I.
When Using a Loaner Defibrillator

The settings on the SETUP windows and SYSTEM SETUP screen can
be changed manually and saved in the defibrillator. When using a loaner
defibrillator during maintenance, set all the settings on the SETUP windows and
SYSTEM SETUP screen of the loaner defibrillator to the same as the settings of
the defibrillator which will be checked or repaired.
The energy setting and alarm settings of the AED mode may be customized too.
Make sure that the SETUP settings, energy setting in the AED mode and alarm
settings on the loaner defibrillator are correct.
NOTE
If you do not use a loaner defibrillator during maintenance and change
the defibrillator settings during maintenance, make sure to return the
settings after maintenance and turn the defibrillator off. The settings are
applied immediately after changing.
Copying the Settings to the Loaner Defibrillator

1. Insert the SD card into the defibrillator which will be checked and save
the settings using “57. Save Settings”on the SYSTEM SETUP screen. For
details, refer to the Administrator’s Guide.
2. Remove the SD card from the defibrillator and insert it into the loaner
defibrillator. Load the settings from the SD card using “56. Load Settings”
on the SYSTEM SETUP screen. For details, refer to the Administrator’s
Guide.

4. MAINTENANCE
Checking the Appearance
Check the following.
Defibrillator
• The defibrillator is not dirty.
• The defibrillator is not cracked or damaged.
• No labels are removed or torn.
• No connectors or switches are cracked or loose.
• Blood or chemical on the defibrillator is cleaned.
Power Cord
• A specified 3-prong power cord is used.
• The metal parts on the connector are not deformed.
• There are no scratches on the cable and cable cover is not torn.
• Using a tester, check that the protective earth is not broken.
External Paddles
• Resin of the external paddles and electrodes for the adult are not cracked or
broken.
• No scratches or cracks on the curled cable or cable mold.
• Paddle electrodes and the metal plates on the paddle holder are not rusted,
dirty, rotten or damaged.
• Confirm that the shock button on the paddle is not removed when pulling it. If
the button is removed, the button must be replaced.
Accessories
• Cables are not broken, bent abnormally or cut.
• Connectors are not damaged or cracked.
• Pins on the connector are not deformed.
• Screws are not loose.
• Pad adapter is not expired.
The life time of the pad adapter is two years. Replace the pad adapter
immediately if it is expired.

4. MAINTENANCE
Checking the SB-831V Battery Pack
Appearance
Check the following and if the battery pack is faulty, replace it.
• No damage or crack on the battery pack. 4
• No labels are removed or torn.
• The battery pack is not expired.
The life time of the battery pack is two years. Replace the battery pack
immediately if it is expired.
Calibration
Perform the battery calibration once a month using “2. Battery Calibration” on
the SYSTEM SETUP screen. For details, refer to the Administrator’s Guide.

4. MAINTENANCE
Checking the Defibrillator
Connecting the Checker and Turning the Defibrillator On

For connection, also refer to the AX-103V defibrillation analyzer Operator’s
Manual.
1. Connect the AX-103V defibrillation analyzer and TEC-8300 series

defibrillator using the JC-906P ECG connection cord and the BR-903P
electrode lead.
TEC-8300 series
defibrillator
JC-906P ECG connection cord
BR-903P electrode lead
Simulated ECG is output from the colored

terminals on the AX-103V defibrillation analyzer.
C: Chest
F: Left foot
L: Left hand
R: Right hand AX-103V
RF: Right foot defibrillation analyzer
Power switch
2. Turn the defibrillation analyzer on. The simulated ECG is output from the
defibrillation analyzer.
3. Turn the defibrillator control dial to the MONITOR position and confirm that
there no abnormalities such as abnormal sound, smell or excess heat.
4. Set the lead to “II” by pressing the LEAD function key.
Wait for several seconds then confirm the following.

• There are no error messages on the defibrillator screen and ECG is
displayed correctly.
• The defibrillator screen is not dark.
Lead II

4. MAINTENANCE
Adjusting the Sync Sound

QRS sync mark 1. After turning the defibrillator power on, confirm that there is a sync sound
and QRS sync mark blinks synchronized with the ECG on the screen.
2. On the SYNC SOUND setting on the VOLUME SETUP window, confirm

that the sound volume can be changed. For the volume settings, refer to
4
Operator’s Manual Part I.
Checking the Recorder

Record/Stop Key
Press the Record/Stop key on the front panel to record the waveforms.
Confirm that the ECG is recorded correctly and the recording paper feeds
correctly and is not skewed. To stop recording, press the Record/Stop key on
the front panel again.
Date and Time Printed on the Recording Paper

Confirm that the date and time printed on the recording paper is correct. If not,
correct the date and time setting on the DATE AND TIME SETUP window. For
the settings, refer to Operator’s Manual Part I.
Event Key
On the monitoring screen, press the EVENT key to confirm that waveforms for
12 seconds are recorded.
Record/stop key
For details on recording, refer to Operator’s Manual Part I.
Recording Quality
On the System Setup screen, perform “4. RECORDER TEST” and confirm that
the following.
• There are no missing dots.
• The recorded items are not too pale or too dark.
• The width of one cycle of calibration waveform is in the range of 22.5 to 27.5
mm.
For details on the recorder test, refer to the Administrator’s Guide.

22.5 to 27.5 mm
Calibration wave of 25 mm/s

4. MAINTENANCE
Detecting Out of Paper

1. Removing the recording paper from the recorder and close the recorder
cover.
2. Press the Record/Stop key on the front panel to confirm that the
defibrillator operates as follows.
Alarm Operation
Message The “OUT OF PAPER”message is displayed in blue.
Sound There is an alarm sound of “ec” in interval of 20 seconds.
Indicator Lights in blue.
Record/stop key

4. MAINTENANCE
Checking the Defibrillation Function in Manual Mode
Check the defibrillation function in manual mode once a month.
To check charging and discharging, the AX-103V defibrillation analyzer is 4

necessary. When checking the defibrillation function, operate the defibrillator on
the AC power. For AC operation, refer to the Operator’s Manual Part I.
When performing “Checking the Duration of Charging Energy” and “Checking

the Discharged Energy” in this section, operate the defibrillator on the battery
power.
Checking the Connector Off Detection

Paddle contact lamp
1. When using the external paddles, check the paddle contact. When using the
disposable pads, connect the jigs to the defibrillator.
When using the ND-831V external paddles

Put the external paddles on the paddle holder and confirm that the paddle
contact lamp lights in green.
Put the paddles on the paddle holder.
If the paddles contact lamp lights in orange or yellow, clean the paddle
electrodes and the metal plates on the paddle holder.
Paddle electrode
Metal plates for test discharge

4. MAINTENANCE
When using the disposable pads

Using the JC-865V pad adapter and JJ-202V analyzer connection cable*,
connect the defibrillator and the AX-103V defibrillation analyzer.
* An accessory of the AX-103V defibrillation analyzer.
Black Red
JJ-202V
analyzer
connection JC-865V pad adapter
cable
Holder JC-865V pad adapter
JJ-202V
analyzer connection cable JJ-202V
analyzer
connection cable
AX-103V
defibrillation analyzer
2. Turn the defibrillator control dial to the MONITOR position and confirm that
the ECG lead is “PADDLE”.
If other lead is selected, set the lead to “PADDLE” by pressing the LEAD
function key.
3. Turn the paddle connector to the left to unlock the connector and remove
the connector from the defibrillator. Then confirm that the “CONNECT
PADDLES/PADS” message appears on the screen.
Paddle
connector
Unlock Paddle
position connector lock
NOTE
Hold the paddle connector when removing the paddle/pad adapter
from the defibrillator. Holding the part other than paddle connector
may damage the connector or break the paddle/pad adapter cable.
4. Connect the external paddles or pad adapter removed in step 3 to the

defibrillator.

4. MAINTENANCE
Checking the Duration of Charging Energy

Confirm that energy in charged within 5 seconds on AC power operation and
battery power operation using a stopwatch or a second hand of a clock.
AC Power
When using the ND-831V external paddles 4
Paddle contact lamp
Before checking the duration of charging energy, put the external paddles on the
paddle holder and confirm that the paddle contact lamp lights in green.
If the paddles contact lamp lights in orange or yellow, clean the paddle electrodes
and the metal plates on the paddle holder.
Paddle electrode
Put the paddles on the paddle holder. Metal plates for test discharge
When using the disposable pads

Using the JC-865V pad adapter and JJ-202V analyzer connection cable*, connect
the defibrillator and the AX-103V defibrillation analyzer.
Black Red
JJ-202V
analyzer
cable
JJ-202V
analyzer
connection cable
AX-103V
Procedure
1. Install the optional SC-831V AC/DC module in the battery slot B to operate
the defibrillator on the AC power.

4. MAINTENANCE
2. Turn the control dial to the 270 J position.
3. Press the CHARGE/AED button on the front panel to start charging and
measure the time from pressing the button to the “CHARGED” message
appears on the screen and there is a beeping sound. Confirm that the
measured time is within 5 seconds.
CHARGED message Charged energy
WARNING
When charging or discharging, do not touch anything other than the
handles. If any other part of the defibrillator is touched during
charging or discharging, the operator receives an electrical shock.
WARNING
Do not move the defibrillator when any charged energy remains in
the defibrillator. If the defibrillator receives any impact, such as from
falling, it discharges energy that can cause electrical shock.
4. Turn the control dial to the DISARM position to discharge the energy
internally.
Battery Power
1. Remove the optional SC-831V AC/DC module from the battery slot B and
install the optional SB-830V battery pack in either of the battery slot A or B
to operate the defibrillator on the battery power.
This icon indicates remaining
battery power.
2. Confirm that the icon (fully charged) is displayed on the screen. If the
battery pack is not fully charged, charge the battery pack.
3. Do step 2 to 4 of the “AC Power” procedure in the previous and this pages
to confirm that the defibrillator charges the energy correctly on the battery
power operation.

4. MAINTENANCE
Checking the Discharged Waveform

Using the AX-103V or Fluke Impulse 6000D/7000DP defibrillation analyzer and
oscilloscope, check the shape of the discharged energy. Refer to the manuals of
the defibrillation analyzer and oscilloscope together with this manual.
1. Connect the defibrillator and the oscilloscope to the defibrillation analyzer.

4
When the AX-103V is used

Recommended oscilloscope settings
Sensitivity: 0.5 V/div
Sweep speed: 2 ms/div
NOTE
Use the input/output cable to connect the AX-103V defibrillation
analyzer and the oscilloscope.
When using the ND-831V external paddles

TEC-8300 series
defibrillator
WAVE Connector (BNC)

GND
Oscilloscope Input/output cable
Discharged voltage from defibrillator

The discharged waveform of the following WAVE output connector
attenuation is output.
HIGH: 1/2400
LOW: 1/960
You can switch HIGH and LOW using the
SENS button on the defibrillation analyzer.
AX-103V
Input/output cord
When using the disposal pads

TEC-8300 series
defibrillator
Oscilloscope Input/output cable JC-865V

Pad adapter
WAVE output connector
JJ-202V
analyzer connection cable
Black Red
AX-103V
Input/output cord

4. MAINTENANCE
When the Fluke Impulse 6000D/7000DP is used

When the JC-865V disposable pad adapter is used, connect the specified
connector to the JJ-225X checker connection cable (Code No.: 735625).
When the JC-855V disposable pad adapter is used, use the specified cable.
Check the connection polarity so that the displayed discharged waveform

has the following shape.
When using the external paddles

APEX paddle
Connect to SCOPE OUTPUT Oscilloscope
STERNUM paddle
When using the JC-865V disposable pad adapter

APEX
(Blue cable)
STERNUM
(White cable)
JJ-255X

4. MAINTENANCE
2. Turn the control dial to the 270 J position and confirm the following.
• Confirm that the defibrillation mode is MANUAL. If “SYNC mode” is
displayed on the screen, change the mode to MANUAL by pressing the
SYNC button on the front panel.
• Confirm that the ECG lead is PADDLE. If other lead is selected, set the 4
lead to “PADDLE” by pressing the LEAD function key.
VF TEST button
3. Turn the defibrillation analyzer on and press the VF TEST button on the
defibrillation analyzer to output the simulated VF waveform. Confirm that a
VF waveform is displayed on the screen.
Confirm that a simulated VF waveform is displayed.
POWER button
4. Press the charge button on the APEX paddle or CHARGE/AED button on

the front panel to start charging.
Charge button
During charging, there is a continuous buzzing sound and the “CHARGING”

message appears on the screen.

4. MAINTENANCE
NOTE
While charging the energy, do not remove the battery pack from the
defibrillator.
Currently charged energy. The value

increases while charging.
Shock buttons blink.
When charging is completed, there is a continuous beeping sound, the
“CHARGED” message appears on the screen, and the shock buttons on the
external paddles blink.
When using the pad adapter and JJ-202V analyzer connection cable, the
CHARGE/AED button blinks.
Do not touch anything other than handle.
WARNING
WARNING
Shock buttons
5. After confirming that the shock buttons blink, press both shock buttons on
the paddles at the same time to discharge the energy.
When using the pad adapter and JJ-202V analyzer connection cable, press
the blinking CHARGE/AED button firmly.
NOTE
Do not discharge the energy with external paddle electrodes pressed
against each other. This may damage the defibrillator.
WARNING
Do not discharge with the paddles in the air. This may cause
electrical shock to the operator or damage the defibrillator.

4. MAINTENANCE
Using the oscilloscope, confirm that the waveform from the AX-103V
defibrillation analyzer is biphasic.
Waveform output from the WAVE connector
6. Confirm that normal ECG is displayed on the screen.

Confirm that normal ECG is displayed.
Checking the Discharged Energy

On AC power operation and battery power operation, confirm that the discharged
energy is within range the specified by IEC. Use the optional ND-831V external
paddles for this check. When the ND-831V external paddles are not used, skip
this check.
Connect the defibrillator to the AX-103V defibrillation analyzer and turn the
defibrillation analyzer on.
TEC-8300 series
defibrillator
POWER button
AX-103V

4. MAINTENANCE
AC Power
Install the optional SC-831V AC/DC module in the battery slot B to operate the
defibrillator on AC power.
NOTE
Set the defibrillation mode to SYNC MODE for this check.
Perform defibrillation with the every energy setting (2, 3, 5, 7, 10, 15, 20, 30, 50,
70, 100, 150, 200 and 270 J). To change the energy setting, turn the control dial
on the front panel.
For details on defibrillation, refer to “Checking the Discharged Waveform” in

this section or the Operator’s Manual Part I.
Confirm the measured energy
on this display. For each energy setting, confirm that the energy is charged as set on the control
dial and energy measured by the AX-103V defibrillation analyzer is as follows.
Energy Accuracy According to the IEC 60601-2-4

Within ±15% or ±3 J of the energy set by the control dial, whichever greater.
SENS button
Set the measurement range
depending on the energy set by NOTE
the control dial.
• When confirming the discharged energy on the AX-103V defibrillation
analyzer, change the measurement range as follows. You can
change the measurement range by pressing the SENS button on the
0 to 70 J: LOW
100 to 270 J: HIGH
• When you discharge the energy repeatedly in a short period, repeat the
following cycle; discharge the energy three times in one minute then
leave the defibrillator for one minute without discharging.
Battery Power
Operate the defibrillator on the battery power for this check.
NOTE
• Set the defibrillation mode to SYNC MODE for this check.
• Set the measurement range of the defibrillation analyzer to HIGH.
Turn the control dial to the 270 J position and discharge the energy.


4. MAINTENANCE
Confirm that the energy is charged as set on the control dial and energy measured
by the AX-103V defibrillation analyzer is as follows.
on this display.
Within 270 J ±15%
4
SENS button
Set the measurement range to HIGH.
Checking the Discharge for When Using the Disposable Pads

Confirm that the discharged energy is within the range specified by IEC on AC
power operation.
1. Using the JC-865V pad adapter and JJ-202V analyzer connection cable*,
connect the defibrillator and the AX-103V defibrillation analyzer. Then
turn the defibrillation analyzer on by pressing the POWER button of the
POWER button
Black Red
JJ-202V
analyzer
cable
JJ-202V
analyzer
connection cable
AX-103V
NOTE
• Set the measurement range of the defibrillation analyzer to HIGH.
2. Turn the control dial to the 270 J position and discharge the energy.
For details on defibrillation, refer to “Checking the Discharged Waveform”

in this section or the Operator’s Manual Part I.

3. Confirm that the energy is charged as set on the control dial and energy
on this display. measured by the AX-103V defibrillation analyzer is as follows.

Within 270 J ±15%
SENS button
Set the measurement range to HIGH.

4. MAINTENANCE
Checking the Discharge for When Using the Internal Paddles

Confirm that the discharged energy is within the range specified by IEC on AC
power operation.
1. Using the internal paddle adapters*, connect the defibrillator and the AX-
103V defibrillation analyzer. Then turn the defibrillation analyzer on by
pressing the POWER button of the defibrillation analyzer.
POWER button
When the internal paddles are sterilized, use the sterilized internal paddle
adapters to prevent the internal paddles from getting contaminated.
AX-103V
Internal paddle
adapters
Holder
NOTE
• Set the measurement range of the defibrillation analyzer to LOW.
• When you discharge the energy repeatedly in a short period, repeat
the following cycle; discharge the energy three times in one minute
then leave the defibrillator for one minute without discharging.
2. Perform defibrillation with the every energy setting (2, 3, 5, 7, 10, 15, 20,
30 and 50 J). To change the energy setting, turn the control dial on the front
panel.
For details on defibrillation, refer to “Checking the Discharged Waveform”

in this section or the Operator’s Manual Part I.
3. Confirm that the energy is charged as set on the control dial and energy
measured by the AX-103V defibrillation analyzer is as follows.
on this display.
Within ±15% or ±3 J of the energy set by the control dial, whichever greater.
SENS button
Set the measurement range to LOW.
Checking for Changing the Energy Setting After Charging is Complete

Check that the defibrillator operates correctly when you change the energy
setting after charging for defibrillation is complete.


4. MAINTENANCE
1. Charge the energy to 270 J. After charging complete, turn the control dial to
the 100 J position and confirm that the charged energy on the screen changes
to 100 J.
2. Charge the energy to 100 J. After charging complete, turn the control dial to
the 270 J position and confirm that the charged energy on the screen changes
to 270 J.
Checking Internal Discharge

Check that the defibrillator internally discharges the energy correctly.

1. Charge the energy to 270 J, then measure the time from charging complete
to internal discharge using a second hand of watch or a stopwatch. Confirm
that the measured time is within ±5 seconds of the time set on “21. Charge
Holding Time” on the SYSTEM SETUP screen.
2. Charge the energy to 270 J, then turn the control dial to the DISARM
position and confirm that the charged energy changes to 0 J within 15
seconds.
Charged energy

4. MAINTENANCE
3. Charge the energy to 270 J, turn the control dial to the MONITOR position
then turn the control dial to the 270 J position again and confirm that the
charged energy changes to 0 J within 15 seconds.
Monitoring screen
Charged energy
4. Charge the energy to 270 J, turn the control dial to the OFF position to turn
the defibrillator off then turn the control dial to the 270 J position again and
confirm that the charged energy changes to 0 J within 15 seconds.
Turning the defibrillator off then turn it on again.
Charged energy

4. MAINTENANCE
Checking the Synchronized Cardioversion
Check the defibrillation function in sync mode once a month.
To check charging and discharging, the AX-103V defibrillation analyzer is 4

Checking the Synchronized Cardioversion Using the Paddle Lead

When the optional ND-831V external paddles are not used, skip this procedure.
1. Connect the defibrillator to the AX-103V defibrillation analyzer.
TEC-8300 series
defibrillator
AX-103V
2. Turn the control dial to the MONITOR position.
On the PADDLE SETUP window, set the SYNC BY PADDLE setting to

ON. (For SETUP windows, refer to the Operator’s Manual Part I.) Then, set
the lead to PADDLE by pressing the LEAD function key.
3. Turn the defibrillator analyzer on and press the DELAY button on the
DELAY button POWER button
4. Turn the control dial to the 50 J position and confirm that the lead is set to
PADDLE.

4. MAINTENANCE
5. Press the SYNC button on the front panel and confirm the following.
• “SYNC MODE” is displayed on the screen.

• Check that the “ ” line appears on the rising slope of every QRS wave.
The “ ” line indicates that the defibrillator detects the QRS wave.
6. Press the charge button on the APEX paddle or CHARGE/AED button on

the front panel to start charging.
Charge button
Do not touch anything other than handle.

WARNING
WARNING
NOTE
Do not remove the battery pack while the defibrillator is charging energy
for cardioversion.

4. MAINTENANCE
During charging, there is a continuous buzzing sound and the “CHARGING”

message appears on the screen.
Currently charged energy. The

Shock buttons value increases while charging.
4
When charging is completed, there is a continuous beeping sound, the
“CHARGED” message appears on the screen, and the shock buttons on the
external paddles blink.
7. Press both shock buttons on the paddles at the same time to discharge the
energy. Continue pressing the buttons until the energy is discharged.
NOTE
Do not discharge the energy with external paddle electrodes are
pressed against each other. This may damage the defibrillator.
WARNING
Do not discharge with the paddles in the air. This may cause
electrical shock to the operator or damage the defibrillator.
Display 8. On the display on the defibrillation analyzer, confirm that the delay time is
within 60 ms.
Checking the Synchronized Cardioversion Using the ECG Lead

Confirm that synchronized cardioversion is performed correctly when using ECG
acquired by the ECG lead as synchronization source.

4. MAINTENANCE

defibrillator using the JC-906P ECG connection cord and the BR-903P
electrode lead.
When using the external paddles
TEC-8300 series
defibrillator

C: Chest
F: Left foot
L: Left hand
R: Right hand AX-103V
RF: Right foot defibrillation analyzer
When using the disposable pads TEC-8300 series

defibrillator

JC-865V pad adapter

C: Chest JJ-202V
F: Left foot analyzer connection cable
L: Left hand
R: Right hand
Black Red
RF: Right foot
AX-103V
2. Turn the defibrillator analyzer on and press the DELAY button on the
DELAY button POWER button
3. Turn the control dial to the 50 J position and confirm that the lead is set to II.
Lead II

4. MAINTENANCE
Display 4. Do steps 5 to 8 of the “Checking the Synchronized Cardioversion Using the

Paddle Lead” procedure in this section and confirm that the delay time is
within 60 ms.

4. MAINTENANCE
Checking in the AED Mode
Check the defibrillation function in AED mode once a month.
To check charging and discharging, the AX-103V defibrillation analyzer is

Preparation
1. Using the JC-865V pad adapter and JJ-202V analyzer connection cable*,
connect the defibrillator and the AX-103V defibrillation analyzer.
Black Red
JJ-202V
analyzer
cable
JJ-202V
analyzer
connection cable
AX-103V
VF TEST button
2. Turn the defibrillator analyzer on and press the VF TEST button to output
the simulated VF waveform.
POWER button
Checking ECG Analysis in AED Mode, Charge and Discharge

1. Turn the control dial to the AED position and confirm the following.
• “ADULT MODE” is displayed on the screen.
• The energy set on “1. Discharged Energy for Adult” of the System Setup
screen is displayed on the screen.
Energy to be charged

4. MAINTENANCE
2. Press the CHARGE/AED button on the front panel. The analysis starts and
the “Analyzing heart rhythm. Do not touch patient.” message appears on the
screen.
3. Confirm that defibrillator judges that defibrillation is necessary and starts

charging energy.
While charging the energy, the “Shock advised. Charging.” and

“CHARGING” messages appear on the screen and there is a continuous
buzzing sound.
WARNING
During charging or discharging, do not touch the pads or connectors.
Failure to follow this warning causes electrical shock to the operator.
WARNING
NOTE
Do not remove the battery pack while the defibrillator is charging energy
for defibrillation.

4. MAINTENANCE
When charging is complete, there is a continuous beeping sound, the “Do

not touch patient. Press the flashing SHOCK button.” and “CHARGED”
messages appear on the screen, and the SHOCK button blinks.
Charged energy
4. After charging complete, press the SHOCK button on the front panel to
discharge the energy.
NOTE
Firmly press the SHOCK button.
5. Confirm that normal ECG is displayed on the screen and the number of
performed defibrillation (once) is displayed.
Confirm that normal ECG is displayed on the screen.
The number of performed defibrillation
Checking the Display

While doing the “Checking ECG Analysis in AED Mode, Charge and Discharge”
procedure in this section, confirm that the messages and instructions are
displayed correctly. For details on the messages and instructions, refer to
Checking the Voice Instruction

While doing the “Checking ECG Analysis in AED Mode, Charge and Discharge”
procedure in this section, confirm that there are voice instructions and they are
correct. For details on voice instructions, refer to Operator’s Manual Part I.

4. MAINTENANCE
Checking the Pacing Function
Check the pacing function once a month.
To check the pacing function, the AX-103V defibrillation analyzer is necessary. 4
Preparation
defibrillator using the following.
• JC-865V pad adapter
• JJ-202V analyzer connection cable*
• JC-906P ECG connection cord
• BR-903P electrode lead
JC-906P ECG connection cord TEC-8300 series

defibrillator
JC-865V pad adapter
JC-865V pad adapter

AX-103V
JJ-202V
analyzer
connection cable
Simulated ECG is output from the colored Black Red

C: Chest JJ-202V
F: Left foot analyzer
L: Left hand connection
R: Right hand cable
RF: Right foot
Holder
2. Turn the defibrillation analyzer on. The simulated waveform of 60 bpm is

output from the colored terminals on the AX-103V defibrillation analyzer.
POWER button

4. MAINTENANCE
Checking the Pacing in Fixed Mode

1. Turn the control dial to the FIX position, set the ECG lead to “II” and
confirm the following.
• No error message on the screen.
• “FIXED MODE” is displayed on the screen.
• ECG waveform from the defibrillation analyzer is displayed on the screen.
ECG waveform from the defibrillation analyzer.
2. Set the pacing rate to 80 ppm by pressing the PACING RATE Up/Down key
on the front panel. The selected rate appears on the message window.
3. Set the intensity to 100 mA by pressing the PACING OUTPUT Up/Down

key on the front panel. The selected intensity appears on the message
window.
4. Press the START/STOP key on the front panel to start pacing.
NOTE
Pacing starts 3 seconds after the START/STOP key on the front panel
is pressed.
Then confirm the following.

• The “PACING” message appears.
• “ ” mark appears below the ECG waveforms in interval of 80 times per
minute and the PULSE lamp blinks synchronized with pacing.
• Pacing is performed regardless of whether there are QRS or not.
Pacing pulse
output point
5. Press the START/STOP key on the front panel to stop pacing.

4. MAINTENANCE
Checking the Pacing in Demand Mode

1. Turn the control dial to the DEMAND position, set the ECG lead to “II” and
confirm the following.
• No error message on the screen.
• “DEMAND MODE” is displayed on the screen.
• ECG waveform from the defibrillation analyzer is displayed on the screen.
4
• Check that the “ ” line appears on the rising slope of every QRS wave.
• QRS sync mark is displayed on the screen and blinks synchronized with
QRS.
QRS sync mark ECG waveform from the defibrillation analyzer.
NOTE
When the pacing rate is set to other than 80 ppm, the heart rate might
not be displayed correctly.

window.
NOTE
is pressed.

4. MAINTENANCE
Then confirm the following.

• “ ” mark appears below the ECG waveforms and the PULSE lamp blinks
synchronized with pacing.
• The “ ” line appears on the rising slope of every QRS wave.
Confirm that marks disappear.

4. MAINTENANCE
Checking the Pacing Rate and Output Current

1. Turn the control dial to the FIX position.

window.

• “ ” mark appears below the ECG waveforms in interval of 80 times per
minute and the PULSE lamp blinks synchronized with pacing.
NOTE
is pressed.
Pacing pulse
output point
Displays pacing rate.
Displays output current. 5. Press the MODE button on the defibrillation analyzer to change the
measurement mode to pacing rate/current intensity measurement mode.
6. Confirm that the measured pacing rate and current intensity are as follows.
• Current intensity (CURRENT): 100 mA ±10%
MODE button • Pacing rate (RATE): 60 ±10 bpm

4. MAINTENANCE
Checking the Monitoring Parameters
Checking the Electrocardiogram (ECG)

Connect the AX-400G vital sign simulator to the defibrillator, and check the
accuracy of the heart rate as well as the amplitude of ECGs in each lead.
Additionally, check if the alarm works normally.
After the check, return the current settings to your own settings.
Preparations
1. Connect the AX-400G vital sign simulator to the defibrillator with the
BJ-900P ECG patient cable.
BJ-900P
ECG patient cable
AX-400G Defibrillator
2. Set the following items on the defibrillator. For details on settings on the
system setup window, refer to Administrator’s Guide. For details on SETUP
window, refer to Operator’s Manual Part I.
System Setup Window
Setting Item
26. ECG Leads 10 LEAD
SETUP Window
Window Setting Item

FILTER DIAGNOSIS
ECG SETUP LEAD I II
LEAD I SENS ×1
SpO2 SETUP SYNC SOURCE ECG
RECORDING SETUP RECORDING WAVES ECG
3. Turn the control dial to the MONITOR position to display the monitoring
screen.

4. MAINTENANCE
Checking the Accuracy of the Heart Rate and the Generation of

Synchronous Sound
QRS sync mark
Set the heart rate in ECGs produced from the AX-400G vital sign simulator in
the following way and check that the heart rate displayed on the defibrillator is
within the accuracy shown in the table below. Additionally, check that there is a
sound synchronous with the QRS and QRS sync mark blinks synchronized with
the QRS. 4
Setting on the
Display on the Defibrillator
AX-400G
BRADY 30 28 to 32 beat/min
NORMAL 80 78 to 82 beat/min
TACHY 160 158 to 162 beat/min
Checking the Sensitivity of ECG

Check the amplitude of the lead I, II, III, V1, V2, V3, V4, V5 and V6. Perform
checking for each lead by the following procedure.
1. Set the AX-400G to 1 mV, 0.25 Hz. The signal of 2 mVp-p is output to the
lead II.
2. Press the Record/Stop key on the front panel to start recording.

To stop recording, press the Record/Stop key on the front panel again.
3. For each lead, confirm that the amplitude of rise and fall of the waveform is
as follows.
Lead Amplitude
II 20 ±2 mm
I, III, V1 to V6 10 ±1 mm
Recording Example of Lead II
20 ±2 mm
Recording Example of Lead I, III, V1 to V6
10 ±1 mm

4. MAINTENANCE
4. Press the LEAD function key to change the lead and repeat the steps 2 and 3
for every lead.
Checking the Detection of the Heart Rate and Electrode-Off Alarms

Check that the alarms for the upper and lower limits of the heart rate and for
the electrode-off event are normally generated. For details on settings on the
SETUP window and displayed item on the monitoring home screen, refer to the
1. Set the ECG settings on the defibrillator as follows.
SETUP Window Setting Item

ECG ALARM HR Lower limit: 90
ECG SETUP
LEAD I II
2. Set the heart rate in ECGs produced from the AX-400G vital sign simulator
to “NORMAL 80” and check that the defibrillator works in the following
way.
Alarm Operation of the Defibrillator

Display of the
Numerical data is highlighted.
heart rate
Only when the optional QS-831V upgrade kit for
arrhythmia analysis; Setting “ARRHYTHMIA
Message display ANALYSIS” to “ON” on the ARRHYTH ALARM
SETUP window displays the BRADYCARDIA
message highlighted in yellow.
Alarm sound The alarm sound of “ceg” is generated.
Alarm indicator The alarm indicator blinks in yellow.
3. Check that the defibrillator works in the following way when you remove
any of the R, F or RF lead wires connected to the AX-400G vital sign
simulator.

The “XX LEAD OFF” (XX: removed lead name)
message appears.
Message display
When the RF is removed, the electrode name is not
displayed.
The alarm sound of “ec” is generated in the interval
Alarm sound
of 20 seconds.
Alarm indicator The alarm indicator lights in blue.

4. MAINTENANCE
Checking the IBP

Connect the AX-400G vital sign simulator to the defibrillator to check zero
calibration and the accuracy of the blood pressure value. Check with all MULTI
sockets.
4
Preparation
H-0753 BSS cable for the AX-400G.
H-0753 BSS cable Defibrillator

AX-400G
for the AX-400G
screen.
Checking the Accuracy of Zero Calibration

1. Set the AX-400G vital sign simulator to “CAL 0 mmHg”.
2. Perform zero calibration.

i) Press the MENU function key to open the menu.

4. MAINTENANCE
ii) On the menu, select PRESS SETUP with the or

function key on the right side.
iii) On the sub menu, select CALIBRATION with the or
function key on the left side.
Sub menu Menu
iv) Press the OK function key. After zero calibration is complete, the
“PRESS: ZERO CALIBRATION COMPLETE” message appears on the
screen and there is a “BING bong” sound.
3. Press the BACK function key to display the monitoring home screen.
Then confirm that the IBP value is within –2 to +2 mmHg.
Checking the Accuracy of the Blood Pressure Value

Check the accuracy of the blood pressure value. After performing the zero
calibration, set the blood pressure value produced from the AX-400G vital sign
simulator in the following way and check that the blood pressure value displayed
on the defibrillator meets the requirement of the table below.
Setting on the AX-400G Display on the Defibrillator

10 mmHg 8 to 12 mmHg

4. MAINTENANCE
Checking the Detection of an Connector-Off Alarm

Check that the connector-off alarm is normally generated. While the blood
pressure signal is being entered from the AX-400G vital sign simulator, remove
the connector for the blood pressure cable from the defibrillator and check that
the defibrillator works in the following way.
Alarm Operation of the Defibrillation 4

Message display The “PRESS: CONNECTOR OFF” message appears.
The alarm sound of “ec” is generated in the interval of
Alarm sound
20 seconds.
Checking the CO2 Value

Connect the AX-400G vital sign simulator to the defibrillator and check the CO2
value and alarm with all MULTI sockets. Additionally, check the accuracy of the
CO2 sensor kit, as required.
Preparation
H-0753 BSS cable for the AX-400G.
H-0753 BSS cable

for the AX-400G
screen.
Checking the Accuracy of the Respiration Rate and the CO2 Value
Set the ECG heart rate output on the AX-400G vital sign simulator to
“NORMAL 80” and check that the respiration rate displayed on the defibrillator
is between 18 and 22 count/min and that the CO2 value is between 40 and
46 mmHg.

4. MAINTENANCE
Checking the Detection of an Connector-Off Alarm

Check that the connector-off alarm is normally generated. While the CO2 signal
is being entered from the AX-400G vital sign simulator, remove the connector
for the CO2 sensor kit from the defibrillator and check that the defibrillator works
in the following way.

Message display The “CO2: CONNECTOR OFF” message appears.
Alarm sound
20 seconds.
Checking the Measurement Accuracy of the CO2 Sensor Kit

If the CO2 measurement involves significant error, use the gas for sensitivity
calibration to check the accuracy. To obtain stable measurement accuracy,
perform the accuracy check regularly every six months.
Preparations
Only use the gas cylinder for sensitivity calibration and flow regulator specified
by Nihon Kohden to check the accuracy. Also, prepare a CO2 sensor kit and
airway adapter.
Gas cylinder for sensitivity calibration Flow regulator
CO2 5% sensitivity gas A-4 PR-150
CAUTION
Follow the CAUTION label on the CO2 gas cylinder.
NOTE
• The gas cylinder for sensitivity calibration and flow regulator specified
by Nihon Kohden must be purchased locally. Use CO2 cylinders with the
following specifications.
Manufacturer: Nellcor Puritan Bennett, Scott Medical Products
division of Air Liquide Healthcare, or other
Outlet fitting: CGA 600
Gas component: 5% CO2, 21% O2 and N2 mix
Expiration: 3 years after the gas is packed in the cylinder
Accuracy: ±0.03% absolute
If the above CO2 cylinders are not available in your country, find highly
compressed disposable gas cylinders with the same specifications from
other manufacturers.

4. MAINTENANCE
• The gas cylinder for sensitivity calibration has its expiration date. Using
the gas cylinder whose expiration date has been reached would not
guarantee the accuracy of calibration. Take a look at the expiration date
(EXP. DATE) which is shown on the gas cylinder.
• Only use the PR-150 in which the pressure meter has a full scale
of 700 psi. Using a non-specified flow regulator might damage the
pressure meter. 4
• When disposing of calibration gas after use, please ask the business
from which you purchased the gas for instruction.
Checking the Accuracy of the TG-900P

1. Rotate the flow regulator to attach it firmly to the top of the gas cylinder for
sensitivity calibration.
2. Connect the CO2 sensor kit to the MULTI socket.
3. Connect the airway adapter to the CO2 sensor.
Airway adapter
Align the marks CO2 sensor

4. MAINTENANCE
Pressure meter 4. Let the CO2 gas flow.

Knob Turn the knob of the flow regulator counterclockwise by about a half turn to
Turn the knob
counterclockwise to open. let the CO2 gas flow. Turn the knob slowly.
Slip joint
Connect and disconnect

the sensor to form the
expiratory phase and the
inspiratory phase. (When
disconnected, strongly
shake the CO2 sensor so
that no CO2 gas remains
in the airway adapter.)
5. Form the expiratory and inspiratory phases and display the value of the CO2
partial pressure (preparation).
i) Connect the slip joint and the air adapter (expiratory phase).
ii) Disconnect the air adapter from the slip joint section (inspiratory phase).
iii) Repeat steps i) and ii) three times to display the value of the CO2 partial
pressure.
6. Check the accuracy.

i) Connect the slip joint and the air adapter (expiratory phase).
Check that the value of the CO2 partial pressure displayed on the screen
is between 34 and 42 mmHg. (See the “Supplementary” information on
the next page.)
ii) Disconnect the air adapter from the slip joint section (inspiratory phase).
Check that 0 mmHg is read in the CO2 display area on the defibrillator.
iii) Repeat steps i) and ii) to check the accuracy.
NOTE
Measuring the CO2 value in the TG-900P is based on the inspiratory
compensation method; therefore, the CO2 condensation in inspiratory
mode should be calibrated to 0 mmHg. After the CO2 gas equivalent
to expiratory air is made to flow and the airway adapter is removed
from the slip joint, strongly shake the CO2 sensor so that no CO2 gas
remains (that is, the CO2 gas in the airway adapter shows a reading
of 0 mmHg), with the result that the existing CO2 gas is completely
replaced.
7. After checking the measurement accuracy, firmly turn the knob of the flow
regulator clockwise to stop the CO2 gas.
NOTE
Once the pressure meter of the flow regulator shows a reading of 0,
the gas cylinder for sensitivity calibration should be replaced with a
new one.

4. MAINTENANCE
Supplementary
• The TG-900P is calibrated at a temperature of 37°C in exhaled gas;
therefore, the indication will show a change of approximately –0.4%/°C
at any other temperature. Generally, the gas to be calibrated is low in
temperature and it might indicate a pressure of 40 mmHg.
• With the TG-900P, the unit of 1 atm is used for calibration. The indication
will change at a rate of 1 mmHg/30 hPa in an environment of other than 1
atm.
4
Example 1: Checking the accuracy at high air pressure
Condensation of CO2 calibration gas: 38 mmHg (5%); atmospheric
pressure: an increase of 60 hPa
The measurement is higher by the amount of 1 mm Hg × (60hPa /
30hPa) = 2 mmHg.
Therefore, 40 mmHg is indicated.
Example 2: Checking the accuracy at a high altitude
Condensation of CO2 calibration gas: 38 mmHg (5%); altitude: 1,000 m
Change in atmospheric pressure = 1013 hPa × 0.1 (altitude-based rate of
change in atmospheric pressure) = 101.3 hPa
101.3 hPa / 30 hPa = 3.4 mmHg
38 mmHg – 3.4 mmHg = 34.6 mmHg
Therefore, 34.6 mmHg is indicated.
Checking the Accuracy of the TG-950P/970P

1. Rotate the flow regulator to attach it firmly to the top of the gas cylinder for
sensitivity calibration.
2. Connect the CO2 sensor kit to the MULTI socket.

4. MAINTENANCE
3. Connect the airway adapter to the CO2 sensor.

Airway
adapter
4. Expose the airway adapter placed in the CO2 sensor kit to room air.
CO2 sensor
Align the
marks
5. Follow steps i) to iv) to perform zero calibration of the CO2 sensor (Air
calibration).
i) Press the MENU function key to open the menu.
ii) On the menu, select CO2 SETUP with the or

iii) On the sub menu, select CALIBRATION (AIR) with the or
function key on the left side.
If the calibration method is set to “N2”, change the calibration method to

AIR.
Sub menu Menu
iv) Press OK function key then press the YES function key to start
calibration.
• If calibration cannot be performed, there is a “bong BING” sound.
• When the “CALIBRATION COMPLETE” message is displayed with
a “BING bong” sound, the calibration is complete.
v) Press the BACK function key to display the monitoring home screen.

4. MAINTENANCE
Pressure meter 6. Turn the knob of the flow regulator counterclockwise by about a half turn to
Knob let the CO2 gas flow. Turn the knob slowly.
Turn the knob
counterclockwise to open.
Slip joint 7. Connect the split joint and the airway adapter. Check that the value of the
CO2 partial pressure displayed on the screen is between 36 and 40 mmHg.
8. After checking the measurement accuracy, firmly turn the knob of the flow 4
regulator clockwise to stop the gas.
There is no need to form

the expiratory phase or NOTE
the inspiratory phase.
Once the pressure meter of the flow regulator shows a reading of 0, the
gas cylinder for sensitivity calibration should be replaced with a new one.
Supplementary
• The TG-950P/970P is calibrated at a temperature of 37°C in exhaled gas;
therefore, the indication will show a change of approximately –0.4%/°C
at any other temperature. Generally, the gas to be calibrated is low in
temperature and it might indicate a pressure of 40 mmHg.
• When the TG-950P/970P is used, atmospheric compensation is already
performed. There is no need to read the indication again.
Checking the SpO2 Value

Connect the AX-400G vital sign simulator to the defibrillator to check the SpO2
value and the accuracy of the pulse rate. Additionally, check that the alarm is
normally generated.
You can check the SpO2 software
version with the SpO2 version label After the check, return the current settings to your own settings.
(UR-3908) on the rear panel of the
defibrillator.
When the SpO2 software version is 01-11 or 01-12, it may take about 40 seconds
to display the SpO2 value after the vital sign simulator is connected. This is not a
failure and continue the check.
Preparation
JL-900P SpO2 connection cord and H-0750 SpO2 connection cable.
H-0750 SpO2 connection cable
SpO2 version label
(UR-3908)
JL-900P
SpO2 connection cord
screen.

4. MAINTENANCE
Checking the Accuracy of the SpO2 Value and the Pulse Rate
Check the accuracy of the SpO2 value and the pulse rate.
1. Set the SpO2 window for basic parameters as follows.
Window Setting Item

SpO2 SETUP SYNC SOURCE SpO2
2. Set the SpO2 value produced from the AX-400G vital sign simulator in the
following way and check that the SpO2 value and the ECG displayed on the
defibrillator are within the accuracy shown in the table below. Additionally,
check that there is a sound synchronous with the pulse wave.
Setting on the AX-400G Display on the Defibrillator

97% SpO2 95 to 99% SpO2
SpO2 80% SpO2 78 to 82% SpO2
70% SpO2 66 to 74% SpO2
ECG NORMAL 80 76 to 84 bpm (SpO2-PR)
Checking the Detection of Alarm for the SpO2 Value and a

Connector-Off Alarm
Check that alarms for the upper and lower limits of the SpO2 value and a
connector-off alarm are normally generated.
1. Set the SpO2 settings on the defibrillator as follows.
Window Setting Item

SpO2 SETUP SpO2 ALARM Lower limit: 90
2. Set the SpO2 value produced from the AX-400G vital sign simulator to “80”
and check that the defibrillator works in the following way.

Displaying the SpO2 value Numerical data is highlighted.
Alarm sound The alarm sound of “ceg” is generated.
Alarm indicator The alarm indicator blinks in yellow.
3. Check that the defibrillator works in the following way when you remove the
SpO2 connection cable and the SpO2 connection cord.

Message display The “SpO2: CONNECTOR OFF” message appears.
The alarm sound of “ec” is generated in the interval
Alarm sound
of 20 seconds.

4. MAINTENANCE
Checking the NIBP (TEC-8342/8352 Only)

Confirm that the NIBP can be measured correctly.
NOTE
This procedure provides basic operation check. For details such as
measurement accuracy, refer to “Check NIBP Screen” later in this section.
4
Preparation
1. Connect the YP-963P cuff for adult to the defibrillator using the YN-901P air
hose for adults/children.
NOTE
Connect the cuff and air hose properly. If the air leaks, proper check
cannot be performed.
screen.
Checking the Type of the Connected Cuff

Confirm that correct type of cuff is detected by checking that the home screen
displays the correct cuff type (ADULT/CHILD).
Checking the Measurement Operation and Display of Measured

Value
Wrap the cuff around your own arm and perform the manual measurement to
check the NIBP measurement operation and display on the measured value.
After measurement is complete, confirm that there is a “BING bong” sound and
measured values are displayed on the screen.
Checking the Measurement Stop Function

Check that you can stop the NIBP measurement during measurement.
Wrap the cuff around your own arm and perform the manual measurement and
press the STOP NIBP function button.
Confirm that the cuff is immediately deflated and measurement stops.

4. MAINTENANCE
Checking the Temperature

Connect the AX-400G vital sign simulator to the defibrillator and check the
accuracy of the temperature with the MULTI sockets and TEMP modular jack.
After the check, return the setting to your setting used at your facility.
Preparations
1. Connect the AX-400G vital sign simulator to the defibrillator.
To the TEMP modular jack

Use the AX-800P connection cable which is compatible with the HR10
connector.
AX-800P connection
cable (Code no.095567C)
compatible with the HR10
AX-400G connector Defibrillator
To the MULTI socket

Use the H-0753 BSS cable for the AX-400G.
H-0753 BSS cable

for the AX-400G Defibrillator
AX-400G
screen.

4. MAINTENANCE
Check the Accuracy of Temperature

Set the temperature output from the AX-400G vital sign simulator and make sure
that the temperature shown on the instrument is within the accuracy range shown
in the table below.
Setting on the AX-400G Indication on the Defibrillator

25°C (77.0°F) 24.8 to 25.2°C (76.6 to 77.4°F)
4
37°C (98.6°F) 36.8 to 37.2°C (98.2 to 99.0°F)
44°C (111.2°F) 43.8 to 44.2°C (110.8 to 115.6°F)
Checking the Connector-Off Detection

Make sure that the connector-off is detected. While the temperature signal from
the AX-400G vital sign simulator is being input, disconnect the temperature
connection cord from the MULTI socket. Make sure that defibrillator operates as
follows.

Message display The “TEMP: CONNECTOR OFF” message appears.
Alarm sound
20 seconds.
Checking the Sensor-Off Detection

Make sure that the sensor-off is detected. While the temperature signal from the
AX-400G vital sign simulator is being input, remove the temperature cable plug
from the TEMP socket. Make sure that monitor operates as follows.

Message display The “TEMP: CHECK SENSOR” message appears.
Alarm sound
20 seconds.

4. MAINTENANCE
Checking the AC-831V 12 Lead ECG Unit
When the AC-831V 12 lead ECG unit is installed in the defibrillator, check the
operation of the ECG lead unit.
Connect the AX-400G vital sign simulator to the defibrillator, and check the
12 lead ECG is displayed on the screen. Additionally, check if the alarm works
normally.
Preparations
1. Connect the AX-400G vital sign simulator to the defibrillator with the BJ-
900P ECG patient cable.
BJ-900P
ECG patient cable
2. On the System Setup screen, set “26. ECG Leads” to “10 LEAD”.
screen.

4. MAINTENANCE
Checking the 12 Lead ECG Display

1. Display the 12 lead ECG monitoring screen.
i) On the monitoring home screen, press the MENU function key.
ii) On the menu, select 12 LEAD ECG MEAS with the or
iii) Press the OK function key to display the 12 lead monitoring screen.
4
2. On the 12 lead ECG monitoring screen, confirm the following.
• There are no abnormalities on the display and there is no error message.
• The display is not dark.
Checking the Connector-Off Detection

Make sure that the connector-off is detected.
Dot line appears on the disconnected lead.
While the signal from the AX-400G vital sign simulator is being input,
disconnect each lead from the vital sign simulator. Make sure that defibrillator
operates as follows.
The “XX LEAD OFF” (XX: removed lead name)
message appears.
Message display
When the RF is removed, the electrode name is not
displayed.
Alarm sound
20 seconds.

4. MAINTENANCE
Safety Check
Safety check is performed while the components are connected. You need
to measure three different currents (earth leakage current, enclosure leakage
current, and patient leakage current) in both the normal condition and a single-
fault condition to make sure that the allowable value is not exceeded. You also
need to record the measured values.
NOTE
Performing safety inspection requires a special instrument for measuring
leakage currents.
Example of measuring earth leakage current
AC wall outlet AC power socket Defibrillator
LCC-1101
Leakage current checker
• Make sure that the measured value is within the range below.
Normal condition 500 μA or less
Single-fault condition 1 mA or less
Example of measuring enclosure leakage current
Exposed metallic portion

(Equipotential terminal)
LCC-1101
Single-fault condition 500 μA or less

4. MAINTENANCE
Example of measuring patient leakage current I

(Measurement
terminal for each
applied part) ECG
When using
Before measurement,
wrap each transducer Three-electrode paddles 4
with aluminum foil. lead
Red Green Yellow
LCC-1101
Leakage current checker Short-circuit all the
electrodes before
measurement.
Measure the patient leakage current flowing in the measurement system for each
parameter other than NIBP and CO2. For the ECG, short-circuit all the electrode
leads before measurement. For the other parameters, wrap the transducer with
aluminum foil before measurement.
DC: 10 μA or less
Normal condition
AC: 100 μA or less
Type BF
DC: 50 μA or less
Single-fault condition
AC: 500 μA or less
Normal condition DC/AC: 10 μA or less
Type CF
Single-fault condition DC/AC: 50 μA or less
* If you are using the LCC-1101 leakage current checker as a leakage current
measuring instrument, first measure the current in the DC+AC mode to make
sure that the above DC range is satisfied. If the allowable value is exceeded,
you need to measure the current in the DC mode again; the result is considered
successful if the above DC range is satisfied.

4. MAINTENANCE
External Paddles and Internal Paddles

1. Short the paddles and connect the probe of the leakage current checker to the
shorted paddles.
2. Change the lead to “PADDLE” by pressing the LEAD function key and
check the patient leakage current.
Pad Adapter
1. Connect the pad adapter to the defibrillator and connect the JJ-202V analyzer
connection cable to the pad adapter. Short the analyzer connection cable tips
and connect the probe of the leakage current checker to the shorted tips.
2. Change the lead to “PADDLE” by pressing the LEAD function key and
check the patient leakage current.
ECG (Electrode Lead)

1. Short all the electrode leads and connect the probe of the leakage current
checker to the leads.
2. Change the lead to “I” by pressing the LEAD function key and check the
patient leakage current.
SpO2 Probe
1. Wrap the SpO2 probe with an aluminum foil and connect the probe of the
leakage current checker to the foil.
2. Turn the control dial to the MONITOR position and measure patient leakage
current.

4. MAINTENANCE
Checking the SB-801V Battery Charger
When using the optional SB-801V battery charger, check the charger every 6
months.
4
The numbers uses in the “Inspection Items” section correspond to the numbers
on the maintenance check sheet at the end of this section. Keep the maintenance
check sheet safely after inspection.
Inspection Items
1. Appearance
• The battery charger is not dirty.
• No damage or crack on the battery charger.
• No label is removed or torn.
• The ventilation hole is not clogged with dust.
2. Power Cord
• The provided 3-prong power cord is used.
• The cable jacket is not dirty, damaged or torn.
• The earth lead is not broken (check this using a test equipment)
3. Power-on
Remove the battery packs from the battery slot, turn the power switch on and
check the following.
• The POWER lamp lights.
• The following lamps light for one second and turn off.
- Battery charging lamp
- Battery charge complete lamp
- ERROR lamp
• The fan rotates for a few seconds then stops.
4. Charging
• When the battery pack is inserted in one of the battery slots:
- The battery charging lamp lights.
- Status indicators on the battery pack blink.
• When another battery pack is inserted to the other battery slot:
- The battery charging lamp lights.
- Status indicators on the battery pack blink.

4. MAINTENANCE
Safety Check
Battery packs are not necessary for safety check.
Safety check is performed while the components are connected. You need
to measure two different currents (earth leakage current and enclose leakage
current) in both the normal condition and a single-failure condition to make sure
that the allowable value is not exceeded. You also need to record the measured
values.
NOTE
Performing safety inspection requires a special instrument of measuring
leak currents.
Example of measuring earth leakage current
AC wall outlet AC power socket

This instrument
LCC-1101

Single-fault condition 1 mA or less
Example of measuring contact leakage current (enclosure leakage current)
AC wall outlet AC power socket This instrument
Exposed metallic portion
LCC-1101

Single-fault condition 500 μA or less

4. MAINTENANCE
System Maintenance Screen
Displaying the System Maintenance Screen

1. Turn the control dial to the OFF position to turn the defibrillator off.
4
2. While pressing the Silence Alarms key on the front panel, turn the control
dial to the BASIC CHECK position. Hold the Silence Alarms key until the
SYSTEM SETUP screen appears.
3. On the SYSTEM SETUP screen, while holding the F4 key, press F1 → F3

→ F2 key.
Silence Alarms key
F1 F2 F3 F4 F5 F6
The System Maintenance – Menu screen appears.
System Maintenance – Menu Screen

4. MAINTENANCE
Operation on the System Maintenance – Menu Screen

• To select the item, press the ITEM ↓ or ITEM ↑ function key to move the
cursor and press the OK function key. The selected screen opens.
• To exit the System Maintenance screen, turn the control dial to any position
other than BASIC CHECK.
Saving the Settings before Maintenance (Flash Save Procedure)

Do the following procedure after changing or adjusting any setting in the
Configuration screen and Adjust AD screen to save the changed or adjusted
setting in memory.
CAUTION
Write down the settings or save the settings on the System
Maintenance screen as a bitmap file before changing the settings or
performing “flash save”. Changing settings related to HV, ECG or
battery on the System Maintenance screen might decrease the
performance of the defibrillator.
CAUTION
Do this procedure after any setting in the Configuration screen and
Adjust AD screen is changed or adjusted. The new setting or
adjustment is not applied and saved until the “Flash Save” procedure
is performed. Otherwise, the “D511” error code appears the next time
the power is turned on.
1. In the System Maintenance – Menu screen, select “1. Configuration” with

the ITEM ↓ or ITEM ↑ function key then press the OK function key. The
System Maintenance – Configuration screen appears.
2. Select “8. Flash Save” with the ITEM ↓ or ITEM ↑ function key.

4. MAINTENANCE
3. Press the → function key. The setting changes from “Off” to “Exec” and the
function keys change as follows:
4. Press the OK key to save the changed or adjusted setting in memory.
To cancel saving, press the CANCEL key. 4
To return to the System Maintenance – Menu screen, press the EXIT key.
Changing the Settings to Factory Default

1. In the System Maintenance – Menu screen, select “1. Configuration” with
the ITEM ↓ or ITEM ↑ function key then press the OK function key. The
System Maintenance – Configuration screen appears.
2. Select “10. Default Setting” with the ITEM ↓ or ITEM ↑ function key.
4. Press the OK function key to change the settings to factory default.
To cancel, press the CANCEL function key.
To return to the System Maintenance – Menu screen, press the EXIT

function key.

4. MAINTENANCE
About the Menu Items

There are six items in the System Maintenance – Menu screen.
Item Description
Changes the settings in the following items:
1 Configuration Installed Language, Flash Save, Charge Times Clear,
Default Setting, Jack Temp Option
Changes the A/D values for ECG waveform
2 Adjust AD acquisition, biphasic HV unit, battery voltage and
paddle contact impedance threshold.
Checks the operation of the keys, buttons, LEDs,
3 Check Hardware
recorder, memories, sounds, etc.
Displays the count of external discharges and
5 Operation Time
operation time.
6 Version Up You can upgrade the system program and data.
Displays the characters used in this defibrillator and
7 Debug mode
checks the flash memory.
System Maintenance Screen Flowchart
Menu 1. Configuration
2. Adjust AD 1. Adjust ECG AD

2. Adjust HV AD
3. Adjust Battery AD
4. Adjust Paddle Contact AD
3. Check Hardware 1. Check Key

2. Check LED
3. Check LCD
4. Check Buzzer
5. Check Voice
6. Check Recorder
8. Check Ecg Frequency
9. Check NIBP
10. Check 12 Lead
11. Examination
12. Check Time Constant
5. Operation Time
13. Check MP
6. Version Up
7. Debug mode 1. Check String

4. MAINTENANCE
Default Settings
The factory default settings are underlined.
Screen Item Setting

Configuration Installed Language Select the language or country.
Selection list: English, Japanese, American, Chinese, Spanish, French,
German, Italian, Norwegian, Finnish, Other 1 to 5
Flash Save Select “Exec” to save the current settings in the System Maintenance 4
screen in the flash ROM.
Selection list: Off, Exec
Charge Times Clear Deletes the count of external discharges and operation time.
Default Setting Select “Exec” to return all settings including the alarm settings to the
factory default settings. Before doing this operation, write down the
necessary settings for each item or save the setting screen as a bitmap
file.
Jack Temp Option Select whether to enable temperature monitoring using the modular jack.
Selection list: On, Off
Default setting: Off for TEC-8321
On for TEC-8322, TEC-8332, TEC-8342 and TEC-8352
Adjust AD Gain Adjust the A/D value for the ECG sensitivity.
→ Adjust ECG AD Setting range: 0 to 31 in steps of 1
Offset Adjust the A/D value for the ECG offset.
Setting range: –99 to +99 in steps of 1
Adjust AD CHARGE AD Adjust the A/D value to measure the charged energy in the HV capacitor.
→ Adjust HV AD Setting range: –25 to +25 in steps of 1
TTR AD Adjust the A/D value to measure the TTR (transthoracic resistance).
DELIVERED Adjust the A/D value to measure the delivered energy from the HV
ENERGY capacitor.
Charge Time (AC) Adjust the energy charging time in AC operation.
Charge Time (Batt) Adjust the energy charging time in battery operation.
Adjust AD Auto Adjust Adjust the A/D value of the battery voltage.
→ Adjust Battery AD Slot A Battery Voltage Adjust the A/D value of the voltage that is applied to the battery in
battery slot A.
Slot B Battery Voltage Adjust the A/D value of the voltage that is applied to the battery in
battery slot B.
Battery current Adjust the A/D value of the battery current.
Adjust AD 100 ohm, 200 ohm, Adjust the A/D value to measure the skin-paddle contact impedance for
→ Adjust Paddle 350 ohm 100, 200 and 350 Ω.
Contact AD

4. MAINTENANCE
Configuration Screen
You can set the several default settings for the defibrillator.
To select a setting for “1. Installed Language”

1. Press the ITEM ↓ or ITEM ↑ function key to select “1. Installed Language”.
2. Select the setting with the ← or → function key.
For “1. Installed Language”, the setting changes as follows:

English ↔ Japanese ↔ American ↔ Chinese ↔ Spanish ↔ French ↔
German ↔ Italian ↔ Norwegian ↔ Finnish ↔ Other 1 to 5
To save the settings (flash save procedure)

Make sure to perform “flash save” to save the changed setting in memory. Refer
to “Saving the Settings before Maintenance (Flash Save Procedure)” in this
section.
CAUTION

4. MAINTENANCE
To clear charge times or return all the settings to the factory default
1. Press the ITEM ↓ or ITEM ↑ function key to select “10. Default Setting”.
4
3. Press the OK key to clear the charge times or initialize the settings.
To cancel it, press the CANCEL function key.
NOTE
Make sure to perform “flash save” after changing any settings on the
System Maintenance – Configuration screen. Refer to “Saving the
Settings before Maintenance (Flash Save Procedure)” in this section.
Adjust AD Screen
You can adjust the ECG sensitivity, charge energy, charge time, delivered energy,
TTR and battery voltage settings by changing the A/D value for each item.
• To call up a sub-screen, select the item with the ITEM ↓ or ITEM ↑ function
key then press OK function key.
• To return to the System Maintenance – Menu screen, press the EXIT function
key.
• Make sure to save the settings after adjustment by pressing the SAVE function
key or performing “flash save” procedure. Refer to “Saving the Settings before
Maintenance (Flash Save Procedure)” in this section.

4. MAINTENANCE
Adjust ECG A/D Screen

You can adjust the A/D value for the ECG offset and ECG sensitivity with the
automatic adjustment mode or manual adjustment mode.
Automatic Adjustment
Adjusting ECG Sensitivity
1. Apply a 2 mVp-p, 10 Hz sine wave between lead R (RA) and L (LA)/F (LF).
2. Press the AUTO GAIN function key. The function keys change as follows.
3. Press the START TEST function key.
To cancel adjustment, press the STOP TEST function key.
The ECG sensitivity is automatically adjusted. The temporary A/D values

are determined and displayed.
4. Do the “flash save” procedure to save the changed setting in the flash
memory. Refer to “Saving the Settings before Maintenance (Flash Save
Procedure)” in this section.
CAUTION

4. MAINTENANCE
Adjusting ECG Offset

1. Short-circuit the external paddles.
2. Press the AUTO OFFSET function key. The function keys change as
follows.
4
To cancel adjustment, press the STOP TEST function key.
The ECG offset is automatically adjusted. The temporary A/D values are
determined and displayed.
CAUTION
Manual Adjustment
Adjust the amplitude and/or baseline of the sine wave on the screen to 2 cm
(“0200h” for offset) with the ↓ or ↑ function key. You can print the ECG A/D
screen during adjustment by pressing the Record/Stop key (To stop recording,
press the Record/Stop key again). The temporary A/D values are determined and
displayed on the screen.
Adjusting ECG sensitivity

1. Apply a 2 mVp-p, 10 Hz sine wave between lead R (RA) and L (LA)/F (LF).
2. Select the item to adjust with the ITEM ↓ or ITEM ↑ function key. The
function key change as follows.
3. Adjust the amplitude of the sine wave with the ↓ or ↑ function key.
To return to the Adjust AD screen, press the RETURN function key.
4. Press the SAVE function key or do the “flash save” procedure to save the
changed setting in the flash memory. Refer to “Saving the Settings before

4. MAINTENANCE
CAUTION
Adjusting ECG Offset

1. Short-circuit the external paddles.
2. Select the item to adjust with the ITEM ↓ or ITEM ↑ function key. The
function key change as follows.
3. Adjust the offset with the ↓ or ↑ function key.
To return to the Adjust AD screen, press the RETURN function key.
CAUTION

4. MAINTENANCE
Adjust HV AD Screen
You can adjust the settings for delivered energy, TTR, charged energy and
charging time. To adjust the charging time, a new fully charged battery pack or
power supply is necessary (required voltage: 13 V, 15 A).
WARNING
This procedure must be performed when the delivered energy is out
of the following range when you check delivered energy with the
required delivery checker after replacing the HV capacitor and
biphasic HV unit.
Allowable delivered energy range

Selected energy level
on the delivery checker
2J ± 0.5 J
3J ±1J
5, 7, 10 J ±2J
20 J or more ± 10%
Required delivery checker:

• Nihon Kohden AX-103V
• Fluke Impulse 6000D
• Impulse 7000DP
The checker must be checked for accuracy and performance every year by its
manufacturer or approved electrical safety organization.
1. Check and adjust the charged energy.

i) When the Adjust HV AD screen is displayed, the “SELECT 270J”
message appears on the screen. Place the external paddles or disposable
pads on the electrode plate of the delivery checker.

4. MAINTENANCE
ii) Turn the control dial on the front panel to 270 J. The “PUSH CHARGE
KEY” message appears and the selected energy is displayed beside the
message.
iii) Press the charge button on the APEX external paddle or the CHARGE/
AED button on the front panel. The charged energy is displayed
beside “Charge Energy” and the elapsed time from starting charging is
displayed beside “Charge Time”.
iv) When the energy charging is complete, the “PUSH DISCHARGE KEY”
message appears. Press both shock buttons on the external paddles when
using the external paddles. Press the SHOCK button on the front panel
when using the disposable pads. The TTR AD (ohm) and delivered
energy are displayed.
v) Check the delivered energy displayed on the delivery checker. If the

delivered energy is not 270 J, continue the adjustment procedure.
vi) Select “2. CHARGE AD” with the ITEM ↓ or ITEM ↑ function key. The
function keys change as follows.
vii) Press the ↑ or ↓ function key to change the energy that will be charged
in the capacitor at the 270 J setting. The new CHARGE AD value is
displayed beside “2. CHARGE AD” (Setting range: –25 to +25, The
default setting is 0).
viii) Select “1. Check HV” and repeat steps ii) to vii) until the delivered
energy displayed on the delivery checker is in the range of 267 J to
273 J.
The charging time is automatically measured and displayed at “Charge

Time”.
2. Adjust the AD values for the TTR and delivered energy measurement.
i) Select “3. TTR AD” with the ITEM ↓ or ITEM ↑ function key.
ii) Press the ↑ or ↓ function key so that the TTR value displayed beside “3.
TTR AD” changes 51 Ω to 50 Ω when performing “1. Check HV”.
iii) Select “4. DELIVERED ENERGY” with the ITEM ↓ or ITEM ↑

function key.
iv) Press the ↑ or ↓ function key so that the delivered energy displayed
beside “4. DELIVERED ENERGY” is in the range of 267 J to 273 J.

4. MAINTENANCE
3. If the charging time is more than 5 seconds, do the following steps.
WARNING
Do not repeatedly charge and discharge the energy. Otherwise, the
defibrillator may heat up.
4
For AC operation:
i) Do steps i) to v) in step 1.
ii) Select “5. Charge Time (AC)” with the ITEM ↓ or ITEM ↑ function key.
iii) Press the ↑ or ↓ function key to change the charging time.

(Setting range: –5 to +5).
iv) Repeat steps i) to iii) until the charging time becomes less than
5 seconds.
For battery operation:

v) Insert a new fully charged SB-831V battery pack.
vi) Disconnect the AC power cord from the defibrillator and AC outlet.
vii) Do steps i) to v) in step 1.
viii) Select “6. Charge Time (Batt)” with the ITEM ↓ or ITEM ↑ function
key.
ix) Press the ↑ or ↓ function key to change the charging time. (Setting range:
–5 to +5).
x) Repeat steps vii) to ix) until the charging time becomes less than
5 seconds.
CAUTION

4. MAINTENANCE
Adjust Battery AD Screen

Adjusts the A/D values of the battery voltage that is applied to the battery pack.
To adjust the A/D value of the battery voltage, a power supply is necessary
(required voltage: 14.4 V).
Adjusting Voltage
1. Supply the power to the battery voltage adjustment jig and set the output
voltage to 14.4 V.
2. Insert the jig to the battery slot A of the defibrillator.
3. Display the System Maintenance – Adjust AD – Adjust Battery AD screen.
4. For automatic adjustment:

Select “1. Auto Adjust” with the ITEM ↓ or ITEM ↑ function key and press
the EXEC function key. The voltage that is applied to the battery pack
is automatically adjusted. The temporary A/D value is determined and
displayed beside “2. Slot A Battery Voltage”.
For manual adjustment:

i) Select “2. Slot A Battery Voltage” with the ITEM ↓ or ITEM ↑ function
key. The function keys change as follows.
ii) Adjust the A/D value with the +1 or –1 function key so that the “XX.
XX” display becomes 14.4 V.
5. Press the SAVE function key to save the value.
6. Turn the control dial to the OFF position.
7. Remove the jig from the battery slot A and insert it in the battery slot B.

4. MAINTENANCE
9. For automatic adjustment:

Select “1. Auto Adjust” with the ITEM ↓ or ITEM ↑ function key and press
the EXEC function key. The voltage that is applied to the battery pack
is automatically adjusted. The temporary A/D value is determined and
displayed beside “3. Slot B Battery Voltage”.
For manual adjustment: 4

i) Select “3. Slot B Battery Voltage” with the ITEM ↓ or ITEM ↑ function
key. The function keys change as follows.
ii) Adjust the A/D value with the +1 or –1 function key so that the “XX.
XX” display becomes 14.4 V.
CAUTION
11. To return to the Adjust AD screen, press the MENU function key.
Adjusting Battery Current

1. Supply the power to the battery voltage adjustment jig and set the output
voltage to 14.4 V.
2. Insert the jig to the battery slot A of the defibrillator.
4. Select “4. Slot A Battery Voltage” with the ITEM ↓ or ITEM ↑ function key.
The function keys change as follows.
5. Adjust the battery current with the +1 or –1 function key so that the number
in the right column matches the number in the left column.
6. Press the SAVE function key and turn the control dial to the OFF position to
turn the defibrillator off.

4. MAINTENANCE
Paddle Contact A/D Screen

Adjusts the AD values to determine the threshold of the skin-paddle contact
impedance.
1. Connect the resistance to adjust.
2. Select the resistance with the ITEM ↓ or ITEM ↑ function key.
3. Press the OK function key. The temporary A/D value to determine the
threshold of the skin-contact impedance is automatically adjusted and
displayed beside the selected resistance.
CAUTION

4. MAINTENANCE
Check Hardware Screen

You can check the function of the following hardware in the defibrillator.
• To select an item to check, press the ITEM ↓ or ITEM ↑ function key and press
OK function key.
• To return to the System Maintenance – Check Hardware screen from the
screen for each check item, press the EXIT function key.
• To return to the System Maintenance – Menu screen, press the EXIT function
key.
Check Key Screen

You can check the dial and key operation and status of connected devices.
To check the dial or key operation, turn the dial or press the key. The selected
mode or pressed key is displayed highlighted.
The status for each item is displayed beside the item name.
To return to the System Maintenance – Check Hardware screen, press the F6 key.

4. MAINTENANCE
Check items in the Check Key screen

For Dial and Keys
Part Name Description

Rotary SW Turn the control dial. The selected mode is displayed.
Basic check
Key The name of the key is highlighted when the corresponding key is pressed. Each item
name shows the following keys.
Silence Alarms Silence Alarms key
Record/Stop Record/Stop key
Sync Sync button
Child Child mode button
Pacing Rate
Up Down Pacing rate Up/Down keys
Pacing Current
Up Down Pacing current Up/Down keys
Pacing Start Pacing Start key
Panel
Charge Charge/AED button
Shock Shock button
Paddle Charge Charge button of the external paddle
Shk L R Shock button of each external paddle
F1 to F6 Function key 1 to 6
For Connected Devices
Device Status Description

Paddle State No Connect, External, Connect the pads or paddles to the defibrillator and confirm that the
Internal, Dispo displayed device is correct.
Polarization Normal, NG Connect the polarization check jig to the defibrillator and confirm that
“Normal” is displayed.
Paddle Contact 0_100, 100_200, Connect the impedance check jig to the defibrillator and check the
200_350, Over 350 impedance.
Ecg State
R Off, Connect Connect the lead to check and confirm that “Connect” is displayed for
L Off, Connect the connected lead.
F Off, Connect
V1 Off, Connect
V2 Off, Connect
V3 Off, Connect
V4 Off, Connect
V5 Off, Connect
V6 Off, Connect
Pace Maker Off, On Input pacemaker pulse and confirm that On is displayed.
Pola Normal, NG Connect the polarization check jig to the defibrillator and confirm that
“Normal” is displayed.
Pacer State No Connect, Connect For TEC-8321/8322/8342, confirm that “No Connect” is displayed. For
Transistor Normal, Error TEC-8332/8352, confirm that “Connect” is displayed.
Lead state Off, Connect Confirm that “Normal” is displayed.
Connect a pacing electrode and check that the status correctly changes.
SpO2 State No Connect, SpO2 Connect the SpO2 probe to the defibrillator and check that “SpO2” is
displayed.
MP-1 State No Connect, Press, Connect the device to the MULTI socket and confirm that the displayed
Temp, CO2 device is correct.
MP-2 State No Connect, Press, Connect the device to the MULTI socket and confirm that the displayed
Temp, CO2 device is correct.

4. MAINTENANCE
Device Status Description

NIBP State No Connect, Connect Connect the NIBP cuff to the defibrillator and check that correct type is
No Connect, Adult, displayed.
Neo
Recorder State Paper Exist, Out Of Set or remove the recording paper and check that correct status is
Paper displayed.
Power State
Power-1 Type No Battery, Battery Insert the battery pack or AC/DC module to the battery slot and confirm 4
Exist that the correct device name is displayed for the correct slot.
Power-1 Connect No Connect, Connect
Power-2 Type No Battery, Battery

Exist, AC DC
Power-2 Connect No Connect, Connect
Charge No Charging, Displays the battery pack charging state.

Charging, charged
Supply Supply, No Supply Displays the AC/DC module state for power supply.
SD Card State No Card, Card Exist/ Insert and remove the SD card and confirm that correct status is
RW, Card Exist/RO displayed.
Bluetooth State No Connect, Connect When the optional QI-832V Bluetooth® module is installed, confirm that
“Connect” is displayed.
ZS State No Connect, Connect Not used.
12 Lead State No Connect, Connect When the optional AC-831V 12 lead ECG unit is installed, confirm that
“Connect” is displayed.
MJ-TEMP State No Connect, Connect When a thermistor probe is connected to the TEMP modular jack,
confirm that “Connect” is displayed.
Check LED Screen

You can check the LED function on the defibrillator. The LED lights when the
item is selected and ON function key is pressed. When the AUTO function key is
pressed, all LEDs are checked and lit one by one.
NOTE
Make sure that there are no alarms during check. If you check the LED
when there is an alarm, the LED does not blink or light correctly.

4. MAINTENANCE
• To select an item to check, press the ITEM ↓ or ITEM ↑ function key.

• To return to the System Maintenance – Check Hardware screen, press the
EXIT function key.
Check LCD Screen

You can check the LCD screen. When “3. Check LCD” on the System
Maintenance – Check Hardware screen is selected and the OK function key is
pressed, the screen is displayed in black.
Every time you press the F1 key, the screen color changes as follows.
black → white → color bar → black....
When the F2 key is pressed, the screen color automatically changes as follows.
black → white → color bar → black....
F1 F2 F3 F4 F5 F6
To return to the System Maintenance – Check Hardware screen, press the F6 key.
Check Buzzer Screen

You can check the sound generated by the defibrillator. The voice instruction can
be checked in the Check Voice screen.
NOTE
Make sure that there are no alarms during check. If you check sound
when there is an alarm, alarm sounds are not correctly generated.

4. MAINTENANCE
To Check Automatically
Press the AUTO function key to start checking sound. The sounds for item 1 to
9 are sequentially generated for 1 second. For “1. QRS”, pitch of the sound
automatically changes from 81% to 100% in steps of 1 then returns to 81% after
check.
To Check Manually 4
Select the item to check with the ITEM ↓ or ITEM ↑ function key then press the
OK function key to check the sound. The sound for each item is generated for
1 second.
NOTE
When “1. QRS” or “5. Operation Sound in AED Mode” is selected and the
“ON” key is repeatedly pressed, each sound might not be heard. This is
because those sounds do not continue for 1 second.
• To change the frequency of the QRS sound, press the FREQUENCY function
key.
• To change the frequency of the operation sound in AED mode, press the
FREQUENCY function key.
• To change the pulse width of the operation sound in AED mode, press the
DURATION function key.
• To return to the System Maintenance – Check Hardware screen, press the

EXIT function key.
Check Voice Screen

You can check the voice instructions on this screen.

4. MAINTENANCE
Press the AUTO function key to start playing voice instructions. All voice
instructions are sequentially played.
To Check Manually
Select the instruction to play with the ITEM ↓ or ITEM ↑ function key. Message
in the center of the screen changes every time you press the ITEM ↓ or ITEM ↑
function key.
To play the voice instruction, press the ON function key.
To return to the System Maintenance – Check Hardware screen, press the EXIT
function key.
Message List
Adult mode.
Child mode.
Child mode. If patient is an adult, set the control dial to AED without pressing
the CHILD MODE button.
Adult mode. Stay calm. Follow voice instructions.
Child mode. Follow voice instructions. If patient is an adult, set the control dial
to AED without pressing the CHILD MODE button.
Confirm that patient is not responding and is not breathing.
Remove all clothing from patient’s chest.
Open package and remove pads.
Remove pads from liner and apply to right upper chest and left side as shown.
Check pad cable connection to defibrillator.
Do not touch patient.
Analyzing heart rhythm. Do not touch patient.
Shock advised. Charging.
Charging.
Do not touch patient. Press the flashing SHOCK button.
Shock delivered.
No shock advised.
Heart rhythm changed.
It is safe to touch patient. Start CPR.
Continue CPR.
Do 5 more chest compressions. Do not touch patient.
Check skin contact and cable connection.
Battery empty. Replace battery pack or connect AC power.
Defibrillator not working. Do not use defibrillator. Start CPR.
Remove pads from liner and apply to patient as shown.
Could not analyze heart rhythm.
Shock canceled.
Press AED button.
Use disposable pads.
Testing voice instructions.
Synchronized cardioversion.
Energy was not delivered to patient.

4. MAINTENANCE
Check Recorder Screen

You can check the recorder in the Check Recorder screen. When checking starts,
the following waveforms are printed, then all the text messages which can be
used for recording are printed.
NOTE
If necessary, stop recording when the recorder starts printing text
messages. You can check for missing dots just by checking the
waveforms. Printing all the text messages uses a lot of recording paper.
Check ECG Frequency Screen

You can check the frequency response when acquiring the ECG waveforms
from the external paddles, internal paddles, disposable pads or ECG disposable
electrodes (lead II). The maximum and minimum amplitude are calculated and
displayed on the screen.
• To change the lead, press the LEAD function key.

The lead changes as follows every time you press the LEAD function key.
ECG1 Paddle → ECG1 II LEAD → ECG2 II LEAD → ECG3 II LEAD →
ECG1 Paddle...
• To change the gain, press SENSITIVITY function key.
The gain changes as follows every time you press the SENSITIVITY function
key.
×1/4 → ×1/2 →×1 → ×2 → ×4 → ×1/4...
• When “II LEAD” is selected, you can change the time constant by pressing the
TIME CONSTANT function key. You can select 0.32 or 3.2.
To print the check result, press the Record/Stop key on the front panel.

4. MAINTENANCE
function key.
Check NIBP Screen

Do not add pressure to the NIBP connector (do not give impact to the
defibrillator and do not breathe on the connector) on the defibrillator when
entering the Check NIBP screen and returning to the Hardware Check screen
from the Check NIBP screen.
Select the item to check with the ITEM ↓ or ITEM ↑ function key then press the
OK function key to start check. Finish the test for each check item within
10 minutes.
Pressure Adjust Screen

This screen is for factory use and is not used for maintenance.
To return to the System Maintenance – Check Hardware – Check NIBP screen,

press the EXIT function key.

4. MAINTENANCE
Examination Screen
On this screen, you can check the sensitivity for normal circuit sensor and safety
circuit sensor.
Items on the screen

• Cuff Type (NORM)
Displays the connected cuff (ADULT/CHILD, FINGER, NEONATAL, NOT
CONNECT).
• Cuff Type (SAFE)
CONNECT).
• Cuff Press (NORM)
Displays the pressure for normal circuit.
• Cuff Press (SAFE)
Displays the pressure for safety circuit.
Check Procedure
Use a 3.5 m air hose (for adult) and 700 cc dummy cuff to apply pressure.
Air tank Manometer Adult air hose Defibrillator

(700 cc) (3.5 m)
Apply 100 mmHg, 200 mmHg and 300 mmHg and check that the displayed
value is as follows.
Applied pressure Cuff Press (NORM) Cuff Press (SAFE)

100 mmHg ±3 mmHg ±8 mmHg


4. MAINTENANCE
Safety Device Test Screen

On this screen, we can check the NIBP safety circuit operation.
Items on the screen

CONNECT).
CONNECT).
• Safety Device Action
Displays the cuff pressure at which the safety circuit operates.
• Safety Device Action
Displays the duration that the safety circuit operates. (For adult cuff, time from
the pressure excesses 300 mmHg).
• Safety Device Status
Displays the status of the safety circuit (inactive or active).
Check Procedure
Press the START TEST function key and check the following.
• The cuff deflates.
• “Safety Device Status” changes to “ACTIVE”.
• “Safety Device Action” is 300 to 330 mmHg.


4. MAINTENANCE
Inflation Test Screen

On this screen, we can check the inflation time for the NIBP pump.
Items on the screen

CONNECT).
CONNECT).
• Inflation Time
Displays time to increase the pressure to 200 mmHg.
Check Procedure
Press the START TEST function key to apply 200 mmHg pressure and check that
the inflation time is less than 7 seconds.


4. MAINTENANCE
Deflation Test Screen


Step Deflation Test Screen

On this screen, we can check the deflation speed.
Items on the screen

• Valve 1 Open (50 ms)
Deflation value at the 250 mmHg when valve 1 is open for 50 ms.
CONNECT).

4. MAINTENANCE

CONNECT).
• Deflation Press
Displays test result. 4
Check Procedure
Use a 3.5 m air hose (for adult) and 250 cc dummy cuff to apply pressure for
“Valve 1 Open (50 ms)” and “Valve 1 Open (120 ms)” tests.
Use a 3.5 m air hose (for adult) and 20 cc dummy cuff to apply pressure for
“Valve 2 Open (50 ms)” and “Valve 2 Open (100 ms)” tests.
1. Select the item to check with the ITEM ↓ or ITEM ↑ function key.
3. Check that “Deflation Press” is as follows.

Valve 1 Open (50 ms) 15 ±8 mmHg

Air Leak Test Screen

You can check air leak of the NIBP module.
There are 3 types of tests.

• Pressure Hold Test
Applies 300 mmHg pressure using an external instrument and compare the
pressure 10 seconds after test start with the pressure 20 seconds after test start.
4. MAINTENANCE
• Air Leak Test (Normal)

Applies 300 mmHg pressure using an external instrument and compare the
pressure 30 seconds after test start with the pressure 90 seconds after test start.
• Air Leak Test (Automatic)
Applies 300 mmHg pressure and compare the pressure 60 seconds after test
start with the pressure 120 seconds after test start.
Items on the screen

CONNECT).
CONNECT).
• Elapsed Time
Elapsed time from test start.
• Air Leak
Displays leak pressure.
Check Procedure
1. Select “Pressure Hold Test” with the ITEM ↓ or ITEM ↑ function key.
3. Check that “Air Leak” is 5 mmHg or less.

Air Circuit Test Screen

On this screen, you can check clogging of the air circuit in the NIBP module.

4. MAINTENANCE
Items on the screen

CONNECT).
CONNECT). 4
• Cuff Press (SAFE)
Displays the pressure for safety circuit.
Check Procedure
1. Confirm that cuff or dummy cuff is not connected to the NIBP connector.
3. Check that “Cuff Press (SAFE)” is within ±40 mmHg or less.

Check 12 Lead Screen

On this screen, you can check the optional 12 lead ECG unit.
Items on the screen

• Check Communication
Checks communication status between the 12 lead ECG unit and the
defibrillator.
• Check Memory
Checks 12 lead ECG unit memory.
• Check Input Unit
Checks input circuit of the 12 lead ECG unit.
• Check Calibration
Checks amplifier of the 12 lead ECG unit.

4. MAINTENANCE
Check Procedure
1. Connect all tips of the connection cord to a check jig.
2. Press the AUTO function key. 4 items on the screen are automatically
checked.
3. Check that OK is displayed for each item.
To return to the System Maintenance – Check Hardware screen, press the MENU
function key.
Examination Screen
Not used.
Check Time Constant Screen

You can check the time constant of the ECG amplifier.
Press the START TEST function key. The defibrillator checks the time constant
0.32 and 3.2. The check result is automatically printed on the paper.
To stop checking, press the STOP TEST key.

4. MAINTENANCE
To Check Manually
You can check the time constant by printing the calibration waveforms on the
paper.
1. Select the time constant and lead by pressing the LEAD key. Every time you
press the LEAD key, the time constant and lead change as follows:
time constant: 0.32 s, lead: ECG1 → 4
time constant: 0.32 s, lead: ECG2 →
time constant: 3.2 s, lead: ECG3 → ...
2. Press the Record/Stop key on the front panel and during printing, press the
CAL key to apply the calibration waveforms.
3. Check that the waveforms are calibrated to the baseline and press the
Record/Stop key.
4. Calculate the time constant from the printed waveforms.
function key.
Check MP Screen
On this screen, you can check the MULTI connectors.
Operation Time Screen

This screen displays the number of external discharges and operation time.

4. MAINTENANCE
Version Up Screen
This screen is used to upgrade programs of the defibrillator.
Upgrading can be performed when two battery packs are inserted. The battery
packs must have remaining power of 2/3 or more. You can also upgrade the
defibrillator when the AC power is supplied and a battery pack with remaining
power of 2/3 is inserted. If the “Cannot upgrade. Remaining battery power
is not enough.” message is displayed on the screen, charge the battery before
upgrading.
When an upgrade kit (SD card) is inserted into the SD card slot, the program
versions of the defibrillator and upgrade kit are displayed on the screen.
Upgrade Procedure
1. Select the item to upgrade with the ITEM function key.
2. Press the YES key to install the program. “No” displayed beside the item
changes to “Yes”.
Not to install the selected item, press the NO function key to change “Yes”
beside each item to “No”.
3. Press the EXEC function key to start installation. All programs set to “YES”
are sequentially installed.
To return to the System Maintenance – Menu screen, press the MENU function
key.

4. MAINTENANCE
Debug Mode Screen

Debug mode screens are for factory use.
Check String Screen

This screen is used to check the text messages used in the defibrillator. You
can display the language which is selected in “Installed Language” (System
Maintenance – Menu screen) by pressing the LANGUAGE function key.
• To display the next or previous page, press the ↓ or ↑ function key.

• To jump 5 pages forward or back, press the ↓↓ or ↑↑ function key.
• To return to the System Maintenance – Debug Mode screen, press the EXIT
key.

4. MAINTENANCE
AD Viewer Screen
This screen displays each AD value that the main CPU currently receives.
Displaying the AD
home screen.
2. On the monitoring home screen, press the Silence Alarms key, MENU
function key and CHILD MODE button at the same time. The AD Viewer
window appears.
Every time you press the Silence Alarms key, MENU function key and
CHILD MODE button at the same time, the AD Viewer window changes as
follows.
AD Viewer → AD Viewer (MP) → AD Viewer (REP) → monitoring home
screen...

4. MAINTENANCE
Saving the System Maintenance Screens as Bitmap Files
You can save the System Maintenance screens as bitmap files.
To save the screens as bitmap files: 4

1. Turn the defibrillator off.
2. Insert an SD card into the SD card slot on the defibrillator right side panel.
3. Display the System Maintenance screen to save. Refer to “Displaying the

System Maintenance Screen” in this section.
4. Press the CHILD MODE button on the front panel. The SHOCK button on
the front panel lights.
Wait until the SHOCK button turns off.
5. Turn the defibrillator off and remove the SD card from the SD card slot.

4. MAINTENANCE
Maintenance Check Sheet
Issuance No.
For detailed procedures, refer to “Checking the Defibrillator” to “Safety Check” in this manual.
Facility name Inspection date Person in charge
Address Delivery date Signature
Model Serial number and revision
Check tools Options/Consumables

Product name Serial number Product name Q’ty Product name Q’ty
Overall judgment Conditions of use

[ ] No error Duration of usage: year(s)
[ ] AED is usable but needs to be repaired soon. Used by:
[ ] AED needs to be repaired immediately.
Number Item Result Action

The defibrillator is not dirty.
The defibrillator is not cracked or damaged.
1 No labels are removed or torn. (Labels are readable.)
No connectors or switches are cracked or loose.
Blood or chemical on the defibrillator is cleaned.
Appearance
A specified 3-prong power cord is used.

The metal parts on the connector are not deformed.
2
There are no scratches on the cable and cable cover is not torn.
Using a tester, check that the protective earth is not broken.
3 When using the external paddles, the paddles are not broken.
Connectors are not damaged or cracked.
4
Pad adapter is not expired.
No damage or crack on the battery pack. No labels are removed or torn.
Battery
5
Pack
The battery pack is not expired.

6 The battery pack is calibrated.
7 The defibrillator correctly turns on and the display operates correctly.
8 QRS sync sound is normal and can be adjusted.
Recorder operates correctly.
Defibrillator
Recorded date and time is correct.

Event recording can be performed correctly.
9
There are not missing dots or uneven tone on the recording paper.
Sweep speed of the recording paper is within the specified range.
Out of paper is correctly detected.

4. MAINTENANCE

10 Connector of is correctly detected.
11 Charging time is within 5 seconds.
Defibrillation is performed correctly.
12
The waveform of the discharged energy is biphasic.
Discharged energy when using the external paddles is correct (write the measured value
below): 4
AC operation
2 J: J 3 J J 5 J J
7 J: J 10 J J 15 J J
13 —
20 J: J 30 J J 50 J J
Defibrillation (Manual)
70 J: J 100 J J 150 J J
200 J: J 270 J J
Battery operation
270 J J
Discharged energy when using the disposable pads is correct (write the measured value
14 below): —
270 J J
Discharged energy when using the internal paddles is correct (write the measured value
below):
AC operation
15 —
2 J: J 3 J J 5 J J
7 J: J 10 J J 15 J J
20 J: J 30 J J 50 J J
16 The charged energy can be changed.
17 Internal discharge is correctly performed.
18 The synchronized cardioversion using the paddle lead is correctly performed.
Sync
19 The synchronized cardioversion using the ECG lead is correctly performed.

VF is correctly detected.
20 Charging automatically starts when VF is detected.
AED
Defibrillation is performed correctly.

21 Messages and illustrations are correctly displayed.
22 The defibrillator correctly generates voice instructions.
23 Fixed pacing can be performed correctly.
Pacing
24 Demand pacing can be performed correctly.

25 Pacing output is correct.
Heart rate accuracy is correctly displayed and QRS sync tone is correctly generated.
26 Sensitivity of ECG wave is correct.
Heart rate alarm and ECG connector off alarm are correctly generated.
Zero calibration accuracy for IBP is confirmed.
27 Display accuracy for IBP is confirmed.
IBP connector off alarm is correctly generated.
Display accuracy for the respiration rate and CO2 value is confirmed.
28 CO2 connector off alarm is correctly generated.
Monitoring
Measurement accuracy of the CO2 sensor kit is confirmed.

Display accuracy for the SpO2 value and pulse rate is confirmed and QRS sync tone is
29 correctly generated.
SpO2 upper/lower limit and SpO2 connector off alarm are correctly generated.
NIBP cuff is correctly detected.
30 NIBP measurement is correctly performed and NIBP display is correct.
NIBP measurement can be manually stopped corrrectly.
Display accuracy for temperature is confirmed.
31 Temperature connector off alarm is correctly generated.
Temperature sensor off alarm is correctly generated.

4. MAINTENANCE

12 lead
12 lead ECG is displayed correctly.

32
Lead off alarm is generated correctly.
Normal condition µA
Earth leakage current
Single-fault condition µA
Contact leakage current Normal condition µA
Safety Check
(Enclosure leakage current) Single-fault condition µA

Patient leakage current I Normal condition µA
(Type BF applied part) Single-fault condition µA
Patient leakage current I Normal condition µA
(Type CF applied part) Single-fault condition µA
SB-801V Battery Charger

The battery charger is not dirty.
No part is broken or rattles.
1
No label is removed or torn.
Inspection
The ventilation hole is not clogged with dust.

The provided 3-prong power cord is used.
2 The cable jacket is not dirty, damaged or torn.
The earth lead of the power cord is not broken.
3 The operation at power-on is correct.
4 The battery packs are charged normally.
Normal condition µA
Earth leakage current
Safety
Single-fault condition µA
check
Contact leakage current Normal condition µA

(Enclosure leakage current) Single-fault condition µA
Comments

Section 5 Replaceable Parts List
When ordering parts or accessories from your nearest Nihon Kohden Corporation
representative, please quote the code number and part name which are listed in
this service manual, and the name or model of the unit in which the required
part is located. This will help us to promptly attend to your needs. Always use
Nihon Kohden parts and accessories to assure maximum performance from your
defibrillator.
55
20
5.2
57 54 20
C
C 56 57 19
56
C b 19
S 53
14 15 58
T
7 Z
18
2 H D
6 M
4
5. REPLACEABLE PARTS LIST
5
23
16 C 36 62 32
a 40
33 25
10 60 22
3
U 66
12 13 65
11 52
9
8 66 65
31
1 P
17 34
67
O
59
27
B a
G 61
K 49 50
42
26 Z 24
R 63 35
21
64
F
28
Y
E
29
A 30

38
5
39
V
J
48
48
45
46
51
37
W
44
I
I
41
a
47
43

No. Code No. Q’ty Description

1 6113-913614B 1 Operation SW 3
2 6114-919508A 1 Operation SW 2
3 6114-917608B 2 Operation SW 1
4 6114-917591B 1 CHARGE SW 8300
5 6124-905335B 1 SHOCK SW 8300
6 6122-901067B 1 Front bezel 8300
7 6114-918251B 1 NVI filter 8300
8 6123-903963A 1 LCD filter 8300
9 6113-914195B 1 Energy selector 8300
10 6114-907334 1 Drip proof sheet MIC-2
11 551805 1 D spring 6601
12 674949 1 O ring P-9 (red)
13 6114-907593A 1 MIC holder (2500)
14 6114-909555A 1 Sound filter
15 6111-903424B 1 Front case 8300
16 6123-904383 1 OP panel 8300K
17 6123-904409A 1 Def OP panel (8321K)
17’ 6123-904392A 1 Def OP panel (8332K)
18 6123-904276A 1 Pace blank panel
18’ 6123-904374A 1 Pace OP panel (8332K)
19 6124-906272A 1 Def caution panel (8321K)
20 6124-906263A 1 Def instruction panel (8321K)
21 6124-906156A 1 Slot sign panel
22 6123-904294A 1 ACDC instruction panel
23 6123-904285A 1 Bat instruction panel
24 6124-905897 1 REC guidance panel (8300)
25 6124-906138A 1 Hook blank panel
26 6113-913445B 1 Insulation sheet main
27 6114-917484A 1 SD card cover 8300
28 6111-903433B 1 Bottom case 8300
29 367835 2 Flat rubber feet CK-17
30 6114-920141 2 Front foot TEC
31 6111-903415B 1 Rear case 8300
32 6114-919936 1 Drip proof packing 2
33 6114-919927 1 Drip proof packing 1
34 6113-915586A 1 Option cover 8300 (BLANK)
35 6113-913534B 2 Bottom holder plate
36 6114-918242B 1 Insulation sheet MP
37 6113-913258B 1 Tube main 8300
38 6113-913249B 1 Tube sensor 8300
39 6114-920025 1 Pump packing
40 6114-916939B 1 TEMP cap
41 6114-916921B 1 TEMP jack packing
41’ 6114-919517A 1 TEMP blank packing
42 6113-913213B 1 Input packing
43 6112-906892B 1 Input enclosure
44 531337 1 L-shaped joint
45 6114-923111 1 Silicon tube
46 662329A 1 Valve
47 6114-137185 1 12P connector packing
48 6114-137194 4 15P connector packing

No. Code No. Q’ty Description

49 6114-124992A 1 AUX connector part
50 6114-900671 1 DSI CN packing
51 6111-903451B 1 Input frame
52 6123-904204 1 TEC-8321 input panel
52’ 6123-904213 1 TEC-8332 input panel
52’’ 6123-904222A 1 TEC-8352 input panel
53 6111-903861A 1 Paddle cup dispo
54 541576 2 O ring P-3 (silicon) 5
55 6114-124377A 2 Electrode plate
56 6114-035802A 8 Paddle lock packing
57 6114-069677A 8 Paddle lock spring K-718
58 6111-903442B 1 Paddle cup outer
59 6113-913472B 1 Option cover 8300
60 6114-917582B 1 Option packing
61 6124-906129 1 AUX panel (8300)
62 6113-913463B 1 Power PCB holder
63 6114-916886B 2 Power connector packing
64 6114-916877A 2 Power connector holder
65 6114-910214 4 Battery spring 1 (2100)
66 6114-919401A 2 Battery lock plate
67 6114-906977A 1 Sponge 46×25×3
A UR-0414 1 CONTROL board
B UR-0415 1 ECG/PACER board (for TEC-8332/8352)
B’ UR-04151 1 ECG/PACER board (for TEC-8321/8322/8342)
C UR-0416 1 KEY/LED board (for TEC-8332/8352)
C’ UR-04161 1 KEY/LED board (for TEC-8321/8322/8342)
D UR-0417 1 POWER board
E HV-831V 1 Biphasic HV
F UR-0418 1 HV CPU board
G UR-0426 1 AUXOUT board
H UR-0428 1 12L-ECG board
I UR-0429 1 ECG-CONN board
J UR-0430 1 MP2/TEMP/NIBP board (for TEC-8342/8352)
J’ UR-04301 1 MP1 board (for TEC-8321)
J’’ UR-04302 1 MP2/TEMP board (for TEC-8322/8332)
K UR-0431 1 REC/EXT board
L UR-3908 1 SpO2 board
M UR-0315 1 Test load
O WS-831V 1 Recorder unit
P 9000-009732 1 Paddle connector (HCV14A-R-NKD)
Q 9000-004746 1 LCD NL8060BC21-11C
R 9000-004737 1 104PW03F LED DRIVER board
S 671097A 1 Speaker TL-C40U0811
T 671088 1 CSA122 DF13-2S-1.25C(S80)
U 909251A 1 CSA123 microphone assy KUC2133-010930
V 532149B 1 Rolling pump P22D-0003R
W 923119 1 TDS-2XV05B-701
X 515542C 1 N-NIBP-R (red) delivery specification 2120B
Y 9000-008484 1 FI-S20S(W65) Triple Line
Z 9000-008582 2 AFBNCD-P=0.5-K1-50-110 4/6 gold coating
a 9000-008617 1 501330-1400(W110)
b 9000-008644 1 AFBNCD-P=05-K1-34-150 4/6 gold coating

Manufacturer
NIHON KOHDEN CORPORATION NIHON KOHDEN ITALIA S.r.l.
1-31-4 Nishiochiai, Shinjuku-ku Tokyo 161-8560, Japan Via Fratelli Bronzetti 28, 24124 Bergamo, Italy
Phone + 81 3- 5996 -8036 Phone + 39 035-219543
Fax +81 3- 5996- 8100 Fax + 39 035-232546
NIHON KOHDEN UK LTD

North and South America Trident Court 118, 1 Oakcroft Road
Chessington, Surrey KT9 1BD, UK
Phone + 44 20-8391- 6800
NIHON KOHDEN AMERICA, INC. Fax + 44 20-8391- 6809
15353 Barranca Parkway, Irvine, CA 92618, U.S.A.
Toll-free +1-800-325-0283
Phone +1 949- 580-1555 Asia
Fax +1 949- 580-1550
NIHON KOHDEN LATIN AMERICA S.A.S SHANGHAI KOHDEN

Carrera 16 No.93A-36 Of. 802. Bogota D.C., Colombia MEDICAL ELECTRONIC INSTRUMENT CORP.
Phone + 57 1- 300-1742 567 Huancheng Bei Road
Fax +57 1-300-1825 Shanghai Comprehensive Industrial Development Zone
Shanghai 201401, China
NIHON KOHDEN DO BRASIL LTDA. Phone + 86 21-5743- 6998
Rua Gomes de Carvalho Fax + 86 21- 5743-6939
1507-Bloco A 9 andar-cjto 91A Vila Olimpia
CEP 04547-005 Sao Paulo-SP. Brasil NIHON KOHDEN SINGAPORE PTE LTD
Phone +55 11-3841- 9943 1 Maritime Square, #10-34 HarbourFront Centre
Fax +55 11-3044 -0463 Singapore 099253
Phone + 65 6376-2210
Fax +65 6376-2264
Europe
NIHON KOHDEN INDIA PVT. LTD.
308, Tower A, Spazedge, Sector 47, Sohna Road
European Representative
Gurgaon-122 002 Haryana, India
NIHON KOHDEN EUROPE GmbH Toll-free +91 1800-103-8182
Raiffeisenstrasse 10, D-61191 Rosbach, Germany Phone + 91 124-493 -1000
Phone + 49 6003- 827-0 Fax + 91 124-493-1029
Fax +49 6003- 827-599
NIHON KOHDEN MIDDLE EAST FZE
NIHON KOHDEN FRANCE SARL P.O.Box 261516, JAFZA View 19
8, rue Francois Delage, 94 230 Cachan, France Room 308 Jebel Ali Free Zone, Dubai, U.A.E
Phone + 33 1-49-08 -05 -50 Phone + 971 4- 884-0080
Fax +33 1-49- 08-93 -32 Fax + 971 4- 880-0122
NIHON KOHDEN IBERICA S.L. NIHON KOHDEN KOREA, INC.

C/Ulises 75A, E-28043 Madrid, Spain 5F Miso Bldg.
Phone + 34 91- 7-161080 890-47 Daechi-dong, Gangnam-gu, Seoul, 135-280 Korea
Fax +34 91- 3- 004676 Phone + 82 2-3273-2310
Fax + 82 2- 3273-2352
Contact information is accurate as of Jan 2015. Visit www.nihonkohden.com for the latest information.
The model and serial number of your instrument are identified on the rear or bottom of the unit.
Write the model and serial number in the spaces provided below. Whenever you call your representative concerning
this instrument, mention these two pieces of information for quick and accurate service.
Model Serial Number
Your Representative

Manual de Servicio TEC-8300

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SERVICE MANUAL

Defibrillator TEC-8321K/8322K/8332K/8342K/8352K Service Manual

First Edition: 05 Apr 2011

The contents of this manual are subject to change without notice.

Bluetooth® and its logo are trademarks of Bluetooth SIG, Inc.

GENERAL HANDLING PRECAUTIONS.............................................................................. i 3

Section 1 General.................................................................................... 1.1

Service Manual TEC-8300 C.1

Electromagnetic Immunity.................................................................................... 1.19

Section 2 Troubleshooting..................................................................... 2.1

C.2 Service Manual TEC-8300

Section 3 Disassembly........................................................................... 3.1

Service Manual TEC-8300 C.3

Section 4 Maintenance........................................................................... 4.1

C.4 Service Manual TEC-8300

Checking the Electrocardiogram (ECG)............................................................... 4.38 1

Service Manual TEC-8300 C.5

System Maintenance Screen Flowchart..................................................... 4.64

Section 5 Replaceable Parts List........................................................... 5.1

C.6 Service Manual TEC-8300

2. When installing or storing the instrument, take the following precautions:

5. To Shutdown After Use

7. The instrument must not be altered or modified in any way.

8. Maintenance and Inspection

Service Manual TEC-8300 i

In the USA and Canada other warranty policies may apply.

ii Service Manual TEC-8300

3. Effect of direct or indirect electrostatic discharge:

6. Use with other equipment:

7. Use of unspecified accessory, transducer and/or cable:

Service Manual TEC-8300 iii

8. Use of unspecified configuration:

9. Measurement with excessive sensitivity:

iv Service Manual TEC-8300

Warnings, Cautions and Notes

Service Manual TEC-8300 v

Operator’s Manual, Part I General & Defibrillation

Operator’s Manual, Part II Parameter Monitoring

vi Service Manual TEC-8300

Service Manual TEC-8300 1.1

1.2 Service Manual TEC-8300

This service manual provides useful information to qualified service personnel

Models and Functions

Functions TEC-8321 TEC-8322 TEC-8332 TEC-8342 TEC-8352

External paddles Option Option Option Option Option

Functions TEC-8321 TEC-8322 TEC-8332 TEC-8342 TEC-8352

* CO2, invasive blood pressure or temperature monitoring is available.

Service Manual TEC-8300 1.3

General Information on Servicing

Note the following information when servicing the defibrillator.

Disinfection and cleaning

1.4 Service Manual TEC-8300

Handling the defibrillator

Measuring and test equipment

Service Manual TEC-8300 1.5

Service Policy, Service Parts and Patient Safety Checks

Only disassemble the defibrillator or replace a board or unit in an environment

As background knowledge for repair, note the following:

1.6 Service Manual TEC-8300

Patient Safety Checks 1

Service Manual TEC-8300 1.7

Maintenance Equipments and Tools

Item to be Checked Equipment and Tool

1.8 Service Manual TEC-8300