New Aeon7200A User Manual

Aeon7200A Series User Manual
Beijing Aeonmed Co., Ltd.

Statement
Beijing Aeonmed Co., Ltd. (Aeonmed for short) holds the copy rights to this manual,
which is non-public, published, and reserves the rights to keep it as a secure
document. Refer to this manual when operating, maintaining and repairing products
only. Anyone other than Aeonmed may not make it known to others.
Proprietary materials protected by the copyright law are included in this manual.
Any section of it cannot be reproduced, copied, or translated into other languages
without any prior written approval from Aeonmed who reserves the copyright.
Everything written in this manual is considered to be correct. Aeonmed is not legally

responsible for any mistakes printed within and any damages caused by incorrect
installation and operation. Aeonmed does not supply privileges endowed by the
patent law to any other parties. Aeonmed is not legally responsible for the results
caused by patent law breaking and any rights of the third party violating.
Refer to this manual before the product is used. The manual includes operating
procedures which must be performed with cautiously, operations that may result in
non-normal working conditions and the dangers which may damage equipment or
cause bodily harm. Aeonmed is not responsible for the security, reliability and
function of the equipments in case that the dangers, damages and non-normal
phenomenon mentioned in this manual happen. Free repairs for these malfunctions
will not be provided by Aeonmed.
Aeonmed has the rights to replace any content in this manual without notice.
Manufacturer Responsibility:
Aeonmed is responsible for the security; reliability and function of the equipments
when to following conditions are adhered to:
Installation, adjustments, mending and repairs must be performed by individuals

authorized by Aeonmed;
Necessary electrical equipment and the working environment must be in
accordance with the national standards, professional standards and the
requirements listed in this manual;
Equipment must be used as instructed in the operating instructions.
CAUTION: This equipment is not for home use.

i
CAUTION: Malfunctioning equipment may become invalid and cause bodily
injury if a set of effective and approving repairing proposals cannot be submitted by
the institution which is responsible for using this equipment.
The paid theoretical framework diagram will be supplied according to customer

requirements by Aeonmed, plus calibrating method and other information to help
the customer, under the assistance of qualified technicians, repair the equipment
parts where can be done by customer himself based on the stipulation by
Aeonmed.
Warranty:
Manufacturing techniques and materials:
For a period of one year from the date of original delivery, the components and
assemblies of this product is warranted to be free from defects manufacturing
techniques and materials, provided that the same is properly operated under the
conditions of normal use and regular maintenance. The warranty period for other
parts is three months. Expendable parts are not included. Our obligation under the
above warranties is limited to repairing free of charge.
Free Obligations:
Our obligation under the above warranties does not include the freight and other
fees;
Aeonmed is not responsible for any direct, indirect or final product broken and
delay which result from improper use, alteration by using the assemblies
unratified and maintenance by anyone other than Aeonmed;
This warranty does not apply to the followings:
Improper use
Machines without maintenance or machines broken
The label of our original serial number or mark is removed or replaced
Other manufacturers product.
ii
Security, reliability and operating condition:
Aeonmed is not responsible for the security; reliability and operating condition of
this product in case that:
The assemblies are disassembled, extended and readjusted
This product is not operated correctly in accordance with the manual instruction.
The power supply used or operating environment does not follow the
requirements in this manual.
Return
Follow the steps below in case that the product needs to be returned to Aeonmed:
1. Obtain the rights of return

Contact our customer service by informing them the number and type of the
product. The number is marked on the surface of the product. Return is
unacceptable if the number cannot be identified. Enclose a statement of the
number, type and the reason of return as well.
2. Transportation charges
Transportation and insurance charges must be prepaid by the user for transporting
the product to Aeonmed for repairing. (Customers charges are added with regard to
the products sold to non-Chinese mainland users).
Use Notice
Welcome to use our products.
To use this product correctly and effectively, the user must read this user manual
carefully before using this product.
When the user is using this product, this user manual must be understood totally
and observe strictly.
This product is only applied to the use this user manual described.
Only trained and professional service persons are allowed to repair and examine
this product.
If there is any case happened in the process of use, please call us and intense
service will be provided.
If there is any change in product specification, another informs will not be given.
iii
Manufacture: Beijing Aeonmed Co., Ltd.
Registered Address: 11B2, Fengtai Science Park, Beijing, PEOPLESREPUBLIC OF

CHINA
European Shanghai International Holding Corp. GmbH(Europ)

Representative Eiffestrasse 80,20537 Hamburg Germany
Address:
Production No.10, Chaobai St., Yanjiao Development Zone, Sanhe, Hebei

Province, China
address:
P.C.: 100070
Tel: +86-10-83681616
Fax: +86-10-63718989
Web site: Http://www.aeonmed.com/
Service Hotline 800-810-8333
E-mail: service@aeonmed.com
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CONTENTS
1. Product Description ................................................................................................................................... 1
1.1. General Information .......................................................................................................................... 1

1.2. Symbols .............................................................................................................................................. 2
1.3. Abbreviations ..................................................................................................................................... 5
1.4. Warnings and Cautions .................................................................................................................... 10
2. Components ............................................................................................................................................. 16
2.1. Configuration ................................................................................................................................... 16

2.2. Front View ....................................................................................................................................... 17
2.3. Side View ......................................................................................................................................... 22
2.4. Back View ......................................................................................................................................... 23
2.5. The Breathing System module ......................................................................................................... 25
2.5.1. Bellows Assembly Ports ........................................................................................................... 26
2.5.2. Common Gas Outlet ................................................................................................................ 27
2.5.3. Ventilating circulation ............................................................................................................. 28
2.5.4. APL Valve ................................................................................................................................. 29
2.6. Vaporizer-VP300/VP500Optional ............................................................................................ 30
2.7. Anesthetic Gas Scavenging System-AP1000 (Optional) ................................................................... 31
2.8. O2 flush ............................................................................................................................................ 32
3. User Interface .......................................................................................................................................... 33
3.1.1. Main Interface Display ............................................................................................................ 35

3.1.2. The Interface layout without anesthesia gas monitoring........................................................ 36
3.1.3. The Interface layout with CO2 and anesthesia gas monitoring .............................................. 37
3.2. Information of the main interface ................................................................................................... 38
3.2.1. Ventilation mode set and display area .................................................................................... 38
3.2.2. Parameter Set and Display Area .............................................................................................. 39
3.2.3. Alarm Indication area .............................................................................................................. 40
3.2.4. Machine Information Area ...................................................................................................... 40
3.2.5. Waveform display area ........................................................................................................... 42
3.2.6. Patient message area .............................................................................................................. 43
3.2.7. Patient parameter monitoring area ........................................................................................ 44
3.2.8. Anesthesia gas monitoring area .............................................................................................. 44
3.2.9. Shortcut key area .................................................................................................................... 45
3.2.10. General menu layout ............................................................................................................... 46
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4. Pre-operative Preparation ....................................................................................................................... 47
4.1. Installation and Connection ............................................................................................................. 47

4.1.1. Connection of Tubes and Cables ............................................................................................. 47
4.1.2. Installation of Breathing Bag ................................................................................................... 48
4.2. Installing the Absorber Canister ...................................................................................................... 49
4.2.1. When to replace absorbent..................................................................................................... 50
4.2.2. Disassembling Absorber .......................................................................................................... 50
4.2.3. Filling Absorbent...................................................................................................................... 50
4.2.4. Oxygen sensor connection ...................................................................................................... 51
4.2.5. Connection of the anesthetic gas/CO2 monitoring module (optional) ................................... 52
4.2.6. AGSS Installation and Connection ........................................................................................... 54
4.3. Pre-operative Test ........................................................................................................................... 56
4.3.1. Test before Operation ............................................................................................................. 56
4.3.2. Pipeline Gas Supply Test .......................................................................................................... 57
4.3.3. Vaporizer Test ......................................................................................................................... 58
4.3.4. Alarm Test ............................................................................................................................... 58
5. Operating guide ....................................................................................................................................... 61
5.1. Opening ........................................................................................................................................... 61

5.2. System Self-test ............................................................................................................................... 61
5.3. Automatic Leak Test ........................................................................................................................ 62
5.4. Manual Test ..................................................................................................................................... 63
5.5. Patient Type Setting......................................................................................................................... 63
5.6. Ventilation Mode ............................................................................................................................. 66
5.6.2. Parameter and adjustment scope of ventilation mode .......................................................... 68
5.6.3. Ventilation Mode Setting ........................................................................................................ 70
5.6.4. Mode parameter setting ......................................................................................................... 71
5.7. Menu screens .................................................................................................................................. 73
5.7.1. Menu operating logic .............................................................................................................. 73
5.7.2. Alarm setting ........................................................................................................................... 74
5.7.3. System setting ......................................................................................................................... 76
5.7.4. Calibration ............................................................................................................................... 80
5.7.5. Service ..................................................................................................................................... 85
5.8. Breathing LoopFor Aeon7200A................................................................................................ 92
5.9. Closing.............................................................................................................................................. 94
6. Alarm and troubleshooting ...................................................................................................................... 95
vi
6.1. Brief introduction of alarm message ............................................................................................... 96
6.2. Alarm message ................................................................................................................................ 97
6.2.1. Alarm default value and setting range .................................................................................... 97
6.2.2. Technical alarm message table ............................................................................................... 98
6.2.3. Functional alarm message ..................................................................................................... 101
6.2.4. Self-test alarm ....................................................................................................................... 104
6.3. Failure diagnosis ............................................................................................................................ 106
7. Cleaning and Disinfecting ....................................................................................................................... 112
7.1. Cleaning and disinfection of pre-use first ...................................................................................... 114

7.2. Cleanable Breathing System Components ..................................................................................... 114
7.3. Absorber ........................................................................................................................................ 115
7.3.1. Auto cleaning with agent or disinfector ................................................................................ 116
7.3.2. Manual cleaning .................................................................................................................... 116
7.3.3. Advanced Sterilizing .............................................................................................................. 116
7.4. Breathing system ........................................................................................................................... 117
7.5. The Bellows Assembly ................................................................................................................... 117
7.5.1. Disassembling ........................................................................................................................ 118
9 Remove the seal ..................................................................................................................................... 118
7.5.2. Testing Function .................................................................................................................... 118

7.5.3. Cleaning and Sterilizing ......................................................................................................... 119
7.5.4. Regular Maintenance ............................................................................................................ 122
8. User maintenance .................................................................................................................................. 123
8.1. General principle of maintenance ................................................................................................. 124

8.2. Maintenance schedule .................................................................................................................. 124
8.2.1. Appearance checklist............................................................................................................. 125
8.3. Maintenance of O2 sensor ............................................................................................................. 126
8.3.1. Replacement of O2 sensor ..................................................................................................... 126
8.3.2. Main technical parameter of O2 sensor ................................................................................. 126
8.4. Maintenance of fuse ...................................................................................................................... 129
8.5. Battery Maintenance ..................................................................................................................... 130
8.6. Consumptive components replacement ....................................................................................... 131
9. Technical Data ........................................................................................................................................ 132
9.1. Pneumatic Diagram ....................................................................................................................... 132

9.2. System technical data .................................................................................................................... 135
vii
9.3. Electrical diagraph ......................................................................................................................... 135
9.4. Physical data .................................................................................................................................. 137
9.5. Environmental requirement .......................................................................................................... 138
9.5.1. IEC60601-1:2005 classification .............................................................................................. 139
9.6. Input and output............................................................................................................................ 139
9.6.1. Electrical ................................................................................................................................ 140
9.6.2. Pneumatic.............................................................................................................................. 141
9.6.3. Electromagnetic compatibility .............................................................................................. 141
9.6.4. Guidance and manufactures declaration ............................................................................. 143
9.6.5. Recommended separation distances .................................................................................... 148
9.6.6. Compliance correction .......................................................................................................... 150
9.7. Anesthetic ventilator technical specifications ............................................................................... 151
9.7.1. Anesthetic ventilator performance ....................................................................................... 151
9.7.2. Ventilation parameter ........................................................................................................... 151
9.7.3. Gas dynamics ......................................................................................................................... 153
9.7.4. Monitor performance ............................................................................................................ 154
9.8. O2 sensor specification .................................................................................................................. 155
9.9. Gas monitoring module technical specifications ........................................................................... 156
9.9.1. MAC calculation of IRMA/ISA gas analyzer ........................................................................... 156
9.9.2. Mainstream gas monitoring module ..................................................................................... 157
9.9.3. Sidetream gas monitoring module ........................................................................................ 164
10. Appendix ............................................................................................................................................ 170
10.1. Accessories List .............................................................................................................................. 170

10.2. Table .............................................................................................................................................. 171
viii
Anesthesia Machine User Manual
1. Product Description
This manual introduces 2 types of machine, one is Aeon7200A Anesthetic Machine, the other is
Aeon7200 Anesthetic Machine. While about function, Aeon7200As function is more than
Aeon7200, so Aeon7200A Anesthetic Machine, for example, is detail introduced in this manual.
1.1. General Information

Anesthesia Machine is a continuous flow anesthesia system which offers manual or
automatic ventilation, easily adjustable fresh gas delivery, anesthetic agent delivery,
ventilation monitoring, convenient ergonomics, and state-of-the-art safety systems.
In terms of theory of operation, the Anesthesia Machine driven by pneumatics and

controlled by electricity, is a device used to administer to a patient continuously or
intermittently, a general inhalation anesthetic and to maintain a patients ventilation.
The integrated breathing system delivers the mixture of O2, N2O, AIR and
anesthetic agents for patient breathing control, while electrical control system
functions as monitoring patient parameters.
The anesthetic machine is intended for use by licensed clinicians, for patients
requiring anesthesia within a hospital. This product is suitable for infants, children
and adults.
1.2. Symbols
The following table provides descriptions of symbols that are used on the device
and/or within this manual.
Symbol Description Symbol
CAUTION Attention, consult accompanying

documents. Refer to user manual.
Turn on power switch ON
Turn off power switch OFF
"ON" for a part of equipment
"OFF" for a part of equipment
Alternating current (AC)
Direct current (DC)
Dangerous voltage
Earth (ground)
Protective earth (ground)
Equipotentiality
Date of manufacture
2
Do not reuse
Use by
Batch code
Authorised representative in the European community
Temperature limitation
WEEE: Waste Electronic and Electrical Waste
Type B equipment
2: Protected against solid foreign objects of 12.5mm

and greater
1: Protection against vertically falling water drops
Manufacturer
Catalogue number
Serial number
3
Rotation in two directions
Rotate to adjust(increase counter-clockwise)
Lock
Unlock
Insp. flow
Exp. flow
O2 flush O2+
Breathing bag/manual ventilation
Fuse
Read the reading of the top floating-point
Outer power supply has been connected
Recycle
Battery charging condition
4
Alarm mute icon
Alarm icon
Interference many occur in the vicinity of equipment

marked with this symbol
Refer to product instructions
Authorized representative in the European community
This device complies with the requirements of Medical

Device Directive, 93/42/EEC.
1.3. Abbreviations
Abbreviation Definition
AGSS anesthetic gas scavenging system
APL adjustable pressure limiting
BDU basic data unit
C compliance
CGO common gas outlet
cmH2O Centimeters of Water
CO2 carbon oxide
5
Des. Desflurane
EEPROM electrically erasable programmable read only memory
Enf. Enflurane
eTCO2 End-expiratory CO2 concentration
FiO2 Fraction of Inspired Oxygen
Flow-t flow-time wave
Flow flow
Freq Frequency
FreqMIN Minimum Frequency in PS mode
GUI Graphic user interface
Hal. Halothane
I:E Inspiratory to Expiratory Ratio
FiCO2 Inspiratory CO2 concentration
Iso. Isoflurane
IPPV Intermittent positive pressure ventilation
L/min liter per minute
6
L iter
7
MAC Minimum Alveolar Concentration
Manual manual ventilation
PMEAN mean pressure
mL Mill Liter
MRI Magnetic resonance imaging
MV minute volume
N2O nitro oxide
O2 oxygen
Paw airway pressure
Paw-t pressure-time wave
Pb plumbum
PLAT plat pressure
PCV Pressure Control Ventilation
PEEP Positive End Expiratory Pressure
PMEAN mean pressure
PPEAK Peak pressure
PS Pressure Support Ventilation
PTARGET Target Pressure
8
SIMV Synchronized Intermittent Mandatory Ventilation
Sev. Sevoflurane
TINSP Inspiratory Time
TP Inspiratory Pause Time
Trigger flow trigger
TSLOPE Inspiratory Slope Time
VT tidal volume
WDT watch dog timer
P Differential Pressure
9
1.4. Warnings and Cautions

Please read and adhere to all warnings, CAUTIONs and NOTICEs listed here and in the
appropriate areas throughout this manual.
WARNING statement gives important information that, if ignored, could lead directly to
personal injury.
CAUTION statement gives important information that, if ignored, could lead directly to
equipment damage and indirectly to personal injury.
WARNINGAnesthetic machine must only be operated by trained, skilled medical staff.
WARNINGAnesthetic machine must and can only be serviced by Aeonmeds authorized
service representatives.
WARNING: For a full understanding of the performance characteristics of this equipment,
the user should carefully read this manual before operating
All system connections.

All WARNINGs and CAUTIONs.
How to use the machine.
How to test the machine.
WARNING: Do the following things before operating Aeon7200A
Finish all the tests listed in Pre-use Preparation.

Test other systematic parts.
WARNING: Do not use the machine if any test failures. Contact Aeonmeds authorized
service representative for maintaining the machine.
WARNINGAnesthesia Machine is not suitable for use in a magnetic resonance imaging
MRIenvironment.
10
WARNING: To avoid the risk of electric shock, this equipment must only be connected to a
supply main with protective earth.
WARNING: The highest attitude of Aeon7200A anesthesia machine is 4600m.
WARNING: The pipeline inlet pressure of Aeon7200A anesthesia machine must be
280-600kPa.
WARNING: Breathing tube, mask, SUCTION filter and so on, adapter of mainstream CO2
module, water trap of side stream CO2 module etc. are disposable accessories. Before using
check the pipeline to ensure the disposal subassembly is out of using .Check the tube which
will be used before use and avoid reusing.
WARNING: When the suction flow is insufficient, the suction port filter should be checked or
replaced.
WARNING: Do not use anti-static and/or electric breathing tubes or masks; otherwise, they
will be flammable near high frequent surgery equipment.
WARNING: Do not incline the machine at the angle of more than 10 degree.
WARNING: Do not position Anesthesia machine to make it difficult to operate the
disconnection device.
WARNING: Do not service or maintain Anesthesia machine while it is in use with the
patient.
WARNING: Perform the pre-use checkout before operating Anesthesia Machine.
WARNING: Remove all equipment on the top cover before moving the machine. Use the
handle on the machine to move the machine.
11
WARNING: Ensure that the machine does not incline when it is upgrading, downgrading,
turning around or getting across a threshold. Do not push the machine across pipelines, lines or
any barrier on the ground.
WARNING: Remove all the equipments attached at the flank of the machine before
transportation, otherwise, incline of the machine will lead to personnel damage.
WARNING: Apply the castor brakes when the anesthetic machine is in use.
WARNING: Do not put the item over 25 kg on the top board of Anesthesia machine.
WARNING: Do not put the item over 12 kg on the work table of Aeon7200A anesthesia
machine.
WARNING: The whole width of machine should be less than 0.8m when hanging some
stuff.
WARNING: In order to protect patients and users from electrical hazards, it is imperative
that all systems consisting of electrical medical devices and other electrical devices, such as
but not limited to PCs, priters, etc., be mounted exclusively by trained personnel.
WARNING: The medical gas pipeline system malfunction could cause one or more devices
connected to the system stopping their operation; this is not applicable to the anesthesia
machine that only uses cylinders for gas supply.
WARNING: The parts of machine in contact with gas to be inhaled by patients dont contain
phthalates, which are known to be carcinogenic, mutagenic or toxic to reproduction.
WARNING: Possible explosion hazard. Do not operate machine near flammable anesthetic
agents or other flammable substances. Do not use flammable anesthetic agents (i.e., either or
cyclopropane).
WARNING: Only non-flammable anesthetics such as desflurane, sevoflurane, enflurane

and isoflurane, which are compatible to other gas are allowed to use in anesthetic system.
WARNING: Possible fire hazard. Fuses(i.e., additional sockets)must only be replaced by

fuses of the same type and with the same rating.
12
WARNING: Possible electric shock hazard. The machine may only be opened by Aeonmed
qualified or Aeonmed authorized service engineer.
WARNING: Electric shock and fire hazard. Do not clean the machine while it is on and /or
plugged in.
WARNING: Disconnect the power plug from the mains supply before removing the rear
panels or servicing the machine.
WARNING: Independent means of ventilation (e.g. a self-inflating manually powered

resuscitator with mask) must be available whenever the machine is in use.
WARNING: Malfunction of the central gas supply system may cause more than one or even
all devices connected to it to stop their operation simultaneously.
WARNING: Use a cleaning and sterilizing schedule that confirms to your institutions
sterilization and risk-management policies.
Refer to the material safety data as applicable.

Refer to the operation and maintenance manuals of all sterilizing equipment.
A damaged oxygen sensor may lead to leakage of its highly caustic contents
that contain potassium chloride. Wear safety gloves and safety googles per
manufacturers recommendations.
Do not inhale fumes that may result from any sterilization process.
WARNING: Use extreme care while handling the absorbent as it is a caustic irritant.
WARNING: Use care in lifting and manipulating vaporizers during the mounting process as
their weight may be greater than expected, based on their size and shape.
WARNING: All gas supplies should be of medical grade.
WARNING: To avoid endangering a patient, do not perform testing or maintenance when

the machine is in use.
WARNING: After the device replacement is finished, all calibrations must be done again
and only the service engineer is allowed to do this.
WARNING: All gas volume, flow and leakage specifications have been tested under STPD,
except those associated with the Anesthetic Breathing System, which be tested under BTPS.
WARNING: If the anesthetic machine is equipped with Anesthetic Gas Delivery System,
Monitoring Equipment, Alarm System and Production Device, no matter the machine is
13
supplied by separate device or system assembly, the anesthetic machine checklist must be
provided.
WARNING: The medical device connected to the anesthesia system must conform to IEC
60601-1:2005 and IEC 60601-1-2:2007.
CAUTION: For your safety and that of your patients, strictly follow this user manual.
CAUTION: Perform the tests specified on the Pre-use Preparation and, in case of a fault, do
not operate the machine until the fault has been corrected.
CAUTION: Before starting the machine, users must be familiar with the information
contained in the User Manual.
CAUTION: If the machine does not function as described, it must be examined and repaired
as necessary by authorized service representative before being returned to use.
CAUTION: Handle the machine with care to prevent damage or functional faults.
CAUTION: Ensure that the gas supply of the machine always complies with the technical
specifications.
CAUTION: Before clinical use, the machine must be correctly calibrated and the respective
tests must be performed, as described in the User Manual.
CAUTION: After servicing, all calibrations must be performed again and only the
professional service engineer can do this.
CAUTION: The anesthesia system conforms to ISO 80601-2-13:2011.
CAUTION: The anesthesia ventilator used together with anesthesia system conforms to
ISO 80601-2-13:2011.
CAUTION: The anesthesia system is used together with the following monitoring device,
alarm system and protection device:
Conform to the pressure measurement of ISO 80601-2-13:2011;

Pressure limit device in conformity with ISO 80601-2-13:2011;
Conform to the exhale output monitor of ISO 80601-2-13:2011;
Conform to the respiratory system with alarm system of ISO
80601-2-13:2011;
Conform to the O2CO2anesthetic gas monitor of ISO 80601-2-55:2011;
All parts contact with the gas conform to ASTM D5466-01.
14
15
2. Components
2.1. Configuration
Standard configuration: Bellows, Breathing system, flow meter, anesthetic
ventilator, battery.
Optional configuration: Touch screen, O2 sensor, MAC, ACGO, AGSS (Anesthetic

Gas Scavenging System), VP300Enflurane, isoflurane, sevoflurane, interface type:
Selectatec, using double metal sheet to make temperature compensation, Pour-fill
infusion.
2.2. Front View
Figure 2-1 Aeon7200A Front View
17
No. Name No. Name
1 Flowmeter 8 CGO
2 Bellows 9 O2 flush
3 Flow Rotary Knob 10 Screen
4 Gas Supply Gauge 11 Vaporizer
5 Paw Gauge 12 Drawers Assembly
6 APL Valve 13 Caster(with brake)
7 Breathing System
Functional description of components is as follows.
No. Item Description Figure
Counterclockwise rotation
of flowmeter rotary knob
Flowmeter increases the flow;
3
Rotary Knob clockwise rotation of
flowmeter rotary knob
decreases the flow.
Measure gauge gas supply

pressure of N2O, AIR, O2
Gas supply
flowing by airway.
gauge
4
Cylinder gauges can
Cylinder
measure the pressure from
Gauges
N2O, AIR and O2
respectively.
18
Castor(with Lock :Push down

11
brake) Unlock: Lift up
1For Flowmeter
Flowmeter, the mechanical device used to adjust flow control. The flow setting is
displayed to the left of the adjustment knob and also below the corresponding flow
tube on the display.
Anesthesia machine includes three types of flowmeter:
Name Type
Double Tube Flowmeter FM110
4 Tubes Flowmeter FM210
6 Tubes Flowmeter FM310
Figure A Flow meter
19
3Gas supply gauge, cylinder gauge
Gas supply gauge, central gas supply gauges measure the pressure from N2O, AIR
and O2 central supply, as shown in figure B.
Cylinder gauges measure the pressure from N2O, AIR and O2 cylinders. As shown
in figure B
Figure B Gas supply gauge
20
9 Vaporizer Manifold
Anesthesia machine includes two types of vaporizer manifold: single vaporizer

manifold (Aeon7200) and double vaporizer manifold (Aeon7200A), as shown in
figure C.
Figure C Vaporizer manifold
21
2.3. Side View
Fig. 2-4 Aeon7200A Side View
No. Name No. Name
1 Slot 2 AGSS
22
2.4. Back View
Fig. 2-6 Aeon7200A Back View
23
Number Name Number Name
1 Power Switch 7 Battery
2 RS-232 Interface 8 Speaker
3 Fuse 9 Gas inlet
4 Auxiliary mains outlet socket 10 Drive Gas
5 Power Cable 11 Exhaust
6 YOKE
Functional description of components is as follows.
Set power switch to ON to

let gas flow in and open an
aesthetic system.
Power
1 Set power switch to OFF
Switch
and close an aesthetic
system to prevent gas
flowing in.
WARNING: The
connection of electrical
Fuse equipment to the auxiliary
mains outlet socket may
Auxiliary
34 reduce the system safety
mains
level; therefore the
outlet
equipment connected to
socket
the auxiliary mains outlet
socket must conform to the
IEC 60601-1.
24
2.5. The Breathing System module
CAUTION: Any adult anesthetic ventilator system used together with the
anesthetic gas supply system must be in accordance with ISO

8835-2.
Mainly function: store anesthetic gas and O2, exhaust gas, absorb CO2, connect with breathing
airway directly and assist to operate breathing.
Figure 2-7Breathing system module
1 Absorber (Carbon dioxide absorbent) 6 Expiratory valve
Inhalation Port / Patient circuit

2 7 APL valve
connector
3 Manual reservoir bag port 8 PAW Gauge
Expiratory Port/
4 9 Bellows assembly (auto ventilation)
Patient circuit connector
5 Inspiratory valve
25
Figure3-4 the breathing system components function control
Item Diagram Description
One soda lime canisters loaded can be continuously

1 Absorber ----- used for 6-8 hours at full load. The water from the
reaction is drained via the water collector underneath.
Used for setting peak pressure and deflating.

7 APL valve
Adjust range0~70cmH2O.
2.5.1. Bellows Assembly Ports
Figure 2-8 Ports of bellows assembly
1 Driving gas connector
2 Exhaust gas port
3 Breathing system connector
WARNING: Never connect exhaust gas port with sub-atmospheric system
directly. Or else leakage of breathing system generates.
26
2.5.2. Common Gas Outlet
Figure 2-9CGO
Common gas outlet, abbreviated to CGO, is an optional part of Aeon7200AAnesthetic

machine. Turn the hand valve clockwise to let the common gas flow through CGO, Turn the
hand valve counterclockwise, the common gas will flow within the Breathing System.
27
2.5.3. Ventilating circulation
Inhalation primary phase: Exhalation primary phase: Exhalation end phase:
1 Exhalation valve 6 Driving gas 8 Excess gas of patient

circuit
2 Driving gas 7 From patient circuit
3 Gas of patient circuit
4 Pressure-relief valve
5 To patient circuit
28
2.5.4. APL Valve
WARNING: Keep all inlets/cables away from the APL valve, and do not put lines/ cables
underneath the APL valve in order to adjust the APL valve smoothly.
CAUTION: The APL valve is automatically excluded from the breathing system whenever
an automatic ventilation mode is selected.
APL valve has two functions; one is that it limits the maximum pressure during manual
ventilation; the other is that the airway pressure can be exhausted quickly by lifting the APL
valve.
The APL valve has a labeled knob for selecting between 0cmH 2O to 70cmH2O and for
indicating approximate pressure settings. Click sound will be heard when adjusting the APL
valve. In manual mode, the APL valve knob can be rotated to change the pressure threshold at
which gas will flow through the pressure threshold at which gas will flow through the valve and
into AGSS. Clockwise rotation of the APL valve knob increases the pressure threshold, and
counterclockwise rotation of the APL valve knob decreases the pressure threshold. Lifting the
top of the APL valve knob will temporarily relieve pressure. The leakage from the anesthetic
breathing in all operational modes when tested at pressure of 3.0kPa (30cmH2O) is 40ml.
Fig. 2-10 APL Valve
29
2.6. Vaporizer-VP300/VP500Optional
The vaporizer delivers anesthetic agent of accurate concentration to breathing system.
Anesthetic agent of accurate concentration will be acquired by adjusting control knob on the
vaporizer. It has temperature compensation, flow compensation and pressure compensation.
The vaporizer cannot be used for patient with respiration because of the strong interior
resistance. The vaporizer can only use one specific anesthetic agent which can be identified by
the label.
Fig.2-11 Vaporizer
NO. Name NO. Name
1 Canister Body 6 Anesthetic tag
2 Interlock bolt 7 Screw cap
3 lock lever 8 Liquid level indicator
4 control dial 9 Drain valve
5 Release button 10 Drain hole
WARNING: Only dry gas of medical degree can be used on the vaporizer. Any improper
operation of the vaporizer will bring damage to patient.
30
WARNING: The vaporizer should be placed vertically at the vaporizer mounting manifold.
Turn the vaporizer to OFF when it is not used.
CAUTION: The vaporizer used with Aeon7200A must comply with ISO 80601-2-13:2011.
CAUTION: For more operating and maintaining information of the vaporizer, refer to VP300
User Manual.
2.7. Anesthetic Gas Scavenging System-AP1000 (Optional)

Anesthetic gas scavenging system absorbs waste gas exhausted from breathing system and
delivers it to processing system.
Fig.2-12 Anesthetic Gas Scavenging System-AP1000
Number Name Number Name
1 window 5 floater
2 U-bracket 6 Patient inlet
3 canister 7 Pressure release port
4 Flow control knob
WARNING Do not block the pressure relieve hole on top of the gas tank when using
AGSS.
31
CAUTION: The anesthetic gas scavenging system used with Aeon7200A Anesthetic
Machine complies with ISO 80601-2-13:2011.
CAUTION: If the AGSS used together with anesthesia system is produced by other
manufacturer, make sure that the AGSS conforms to ISO 80601-2-13:2011.
CAUTION: For more operating and maintaining information of AGSS, refer to AP1000 User
Manual.
2.8. O2 flush
Figure2-12
As shown in Figure2-10, by pressing the button, high flow of 35L/min--50L/min can be provided
to fresh gas outlet. When O2+ is pressed, between 35 L/min and 50 L/min of O2 flow will be
delivered to the Breathing System. Flush is available at all times when the machine is
connected to a Central Gas Supply System or Back-up Cylinder.
CAUTION When central gas supply or backup cylinder is connected, pres suing O2 flush
will deliver oxygen to breathing system and breathing bag, even the machine is powered off.
32
3. User Interface
WARNING: The anesthesia breathing machine used together with anesthesia system
conforms to ISO 80601-2-13:2011.
For 12.1-inch display, the panel of the anesthetic machine is composed of user interface,
function keys and a knob. Shown in figure 3-1
Figure 3-1 User interface
No Name Description
1 Touch screen Touch screen.
The user interface can display real-time pressure and flow
waveforms, respiratory loop, monitoring data, Electronic Flowmeter
settings and anesthesia System and provides both sound and visual
alarms to assist the user.
2 AC Indicator The indicator is lighted as AC power effectively;
The indicator is dark as AC power failure.
3-1 MANUAL/ In Standby mode, first press MANUAL/AUTO knob, the system switch
AUTO to Manual mode, then secondly switch to IPPV mode.
In automatic mode, first press MANUAL/AUTO knob, the system
switch to Manual mode, then secondly switch to the original mode.
When entering or exiting the Manual mode, the user information area
displays according to the original model.
3-2 MUTE If there is an alarm, press MUTE and the silence will keep for 110
seconds; press the key again, and the silence is cancelled. If the
alarm has a change but the silence less than 120s, the silence will be
cancelled.
4 Knob The user can set the parameter values by rotating the knob and
confirm set values by pressing the knob. Rotating the knob clockwise
increases values and rotating the knob counter-clockwise decreases
values.
CAUTION: The required circumstance of the monitoring of the breathing system as follows:
Circumstance temperature: 25;
Gas temperature: 25;
Gas tidal: 30%;
Gas: O2.
CAUTION: The anesthesia ventilator which is used with the anesthetic system complies
with ISO 80601-2-13:2011.
34
3.1.1. Main Interface Display
Fig 3-2 User Interface
NO. NAME NO. NAME
1 Parameter set and display area 6 Patient message area
2 Anesthetic gas monitoring area 7 Machine information area
3 Ventilation mode set area 8 Shortcut key area
4 Alarm indication area 9 Patient parameter monitoring area
5 Waveform display area
35
3.1.2. The Interface layout without anesthesia gas monitoring
Fig 3-3The Layout of the User Interface
36
3.1.3. The Interface layout with CO2 and anesthesia gas
monitoring
Fig 3-4The Layout of the User Interface
37
3.2. Information of the main interface
3.2.1. Ventilation mode set and display area
3.2.1.1. Ventilation mode display

Name description
Ventilation mode area shows current ventilation mode. The mode setup menu will be open by
clicking the ventilation mode area via touch screen.
3.2.1.2. There are four states for mode button as shown below
Name description Diagram
The normal mode without any operation to the mode button.
Focusing state when rotating the knob to the purpose mode,
the corresponding button will display this state.
Pending state this state is displayed when switching modes.
White state means the current mode that is selected.
38
3.2.2. Parameter Set and Display Area
3.2.2.1. Parameter display

Name description and Diagram
Parameter setting area is located at the bottom of the screen, which are applied for real-time
respiratory parameter adjustment, including 8 setting buttons.
The Ventilation parameters of all models are arranged from left to right, as shown in the chart
below:
Model Parameter1 Parameter 2 Parameter 3 Parameter 4 Parameter 5
Standby Patient type Blank Blank Blank Blank
IPPV VT Freq I:E Tp Blank
PLV VT Freq I:E PLimited Blank
SIMV VT Freq TINSP Trigger Tp
SPONT Trigger FreqMIN Blank Blank Blank
MANUAL AUTO Blank Blank Blank Blank

3.2.3. Alarm Indication area
Name description and Diagram
Alarm indication: when an alarm appears, an alarm bell icon shows in the warning area. For a
senior-level alarm, the alarm bell is red with white lettering. An intermediate-level alarm is
yellow with black lettering. A low-level alarm is blue-green with black lettering. At most, two
alarms can display on the screen at one time.
By pressing MUTE button, an X shows on the alarm icon. Below the alarm bell a countdown
timer appears. The X and countdown second display the same color as the alarm bell.
CAUTION: The flickering frequency of higher priority alarm among all alarms indicates
all alarms, alarm bell and countdown seconds (if any). The alarm information text keeps
own color respectively (if any).
3.2.4. Machine Information Area
Current date indicates at date display area, with format

DD/MM/YY, YY/MM/DD, MM/DD/YY
Current time indicates at the time display area, with 12 hour
or 24 hour format.
NOTE: Time and date format and value can be set in
system setup menu.
40
The description of these icons is as follows.
Power status includes AC power and backup battery state,

which will be always shown. When AC power is normal, the
white plug icon shows consistently without flashing. When net
power is disconnected or fails, the white plug icon disappears.
Battery power 100%
Battery power 75%
Battery power 50%
Battery power 25%
Battery power low (10%)
Battery not connected
41
3.2.5. Waveform display area
Waveform display area is located in the center of the screen, including waveform and breathing
loop.
Waveform name Diagram
Pressure-time
waveform(Paw-t)
Velocity-time waveform
(Flow-t)
Carbon dioxide-time waveform
(CO2-t)
Pressure-Volume
42
Flow-Volume
3.2.6. Patient message area
Patient type shows adult or child.
CAUTION: Patient type setting is conducted under
standby mode.
43
3.2.7. Patient parameter monitoring area
The patient parameter monitoring area is on the right side of

the screen. There are at most four groups of parameters:
pressure group, capacity group, oxygen concentration group
and carbon dioxide concentration group.
3.2.8. Anesthesia gas monitoring area
Gas monitoring parameter displays on the left side of the

screen, including three parameters: primary agent, nitrous oxide
(N2O) concentration, and exhale MAC value.
44
3.2.9. Shortcut key area

The shortcut key area includes shortcuts to alarm settings, system settings, calibration,
engineer mode, gas setting and breathing loop.
CAUTION: Shortcut keys are disabled during power up self-test.
Alarm setting: when user presses alarm setting key, alarm

menu appears. If this button is pressed in open state, alarm
setting menu closes, and returns to the main interface.
System setting: by pressing system setup key, the system

setup menu appears. If this menu is pressed in open state,
system setting menu disappears, and returns to main
interface.
Calibration: by pressing calibration key, the calibration menu

appears. If this button is pressed in open state, calibration
button disappears and returns to main interface.
Service: by pressing service key, the service menu appears. If

this button is pressed in open state, service button disappears
and returns to main interface.
Loops: by pressing Loops key, the loops menu appears. If this

button is pressed in open state, the functional menu
disappears and returns to main interface.
Main Interface: when normal key is pressed, all menus will be

closed to return to main interface.
45
3.2.10. General menu layout
The background of the overall menu is gray with the menu title shown centered, at the top of
the window. Below the menu title there are a number of tabs containing a variety of content
within the menu. In the top, right corner of the window is an "x" button which closes the menu
when pressed. The menu elements include option key, button, label and indicative text, etc.
46
4. Pre-operative Preparation
4.1. Installation and Connection
4.1.1. Connection of Tubes and Cables
Step 1
Connect bellows and absorber cycle with one

corrugated tubing (22).
Fig. 4-1
Step 2
Connect bellows and driving gas output

connector on the rear panel with another tube
(17).
Fig. 4-2
Step 3
Get two repetitious silica gel tubes connect the
one at expiratory port of absorber cycle.
Fig. 4-3
Step 4
Connect the other tubes at inspiratory port of

absorber cycle.
Fig. 4-4
Step 5
The other end of the two tubes should be
connected with Y-piece and simulation lung
(reservoir bag).
The capacity of simulation lung is 3L.
Fig. 4-5
4.1.2. Installation of Breathing Bag
Connect the Manual reservoir bag onto

bag arm of breathing system.
Fig. 4-6
48
4.2. Installing the Absorber Canister
WARNING: Follow the proper security measures:
Do not use the absorber if the anesthetic is chloroform or

trichloroethylene.
Avoid letting the skin or eyes touch the materials in the absorber.
Clean the affected part immediately and seek medical attention if
materials come in contact with skin or eyes.
Do not replace absorber during the period of ventilating.
Replace the absorbent often to prevent the deposition of

non-metabolism gas as the system is not on.
Check the color of the absorbent after finishing each case. The
original color of the absorbent may be restored when not in use.
Refer to the labels of the absorbent for the details.
Carbon monoxide is released if completely dried absorbent contact

with the anesthetic. Replace the absorbent for security.
Perform leakage testing of breathing system in bag control mode

after disassembling the absorber.
The absorber in this system can be used repetitious.
The capacity of each absorber is 1800ml. It is recommended to use Medisorb absorbent.
Only air, oxygen, carbon monoxide, halothane, enflurane, isoflurane, sevoflurane and
desflurane can be used for the absorber.
49
4.2.1. When to replace absorbent
Changed color of the soda lime in the absorbent indicates that it has absorbed the carbon
dioxide; however, this color is not 100% accurate. To decide whether to replace the absorbent,
use CO2 monitoring machine.
Remove the changed-color absorbent immediately. The soda lime will restore its original color
several hours later and that may mislead the operator.
4.2.2. Disassembling Absorber
The absorber is reusable. Follow the disassembling procedures:
Turn clockwise the absorber and then disconnected it according to the explanation on the
absorber.
Fig. 4-7
4.2.3. Filling Absorbent
1 Remove the absorbent of absorber.
2 Cleaning and disinfection refer to section 7.3.
3 Fill the absorber with fresh absorbent after dryness. Wipe soda lime fell on the edge of
absorber, and then install it back. Make sure the air tightness is well, and that no leakage
and spillage.
50
4.2.4. Oxygen sensor connection
Step 1:
Plug one end of T-piece to the inspiratory port

of breathing system.
Fig. 4-8
Step 2:
Plug the oxygen sensor to T-piece.
Fig. 4-9
Step 3:
Plug one end of the oxygen sensor line into the
bottom interface of the sensor. The other end
of the oxygen sensor line should be plug into
the O2 Sensor port on the rear panel.
Fig. 4-10
51
4.2.5. Connection of the anesthetic gas/CO2 monitoring
module (optional)
CAUTION: The anesthetic gas/CO2 monitoring module has mainstream and side stream.
The two types cant be used at the same time.
CAUTION: The anesthetic gas/CO2 monitoring module conforms to ISO 80601-2-55:2011.
4.2.5.1. Connection of the mainstream monitoring module
Step 1
Snap the probe on top of the airway adapter. It
will click into place when properly seated.
Fig. 4-11
Fig. 4-12
Step 2
Connect the RS232 interface of the adapter to
the RS232 interface on the back of the
machine.
Fig. 4-13
52
Step 3
CAUTION: After powering on the system,
a green LED indicates that the probe is ready

for use.
Fig.4-14
Connect the smaller end of the adapter to the
Y-piece connector.
Fig.4-15
Step 4
Connect the other end of the adapter to the
face mask or breathing bag.
Fig.4-16
4.2.5.2. Connection of the sidestream monitoring module

Step 1
Take out the sampling tube and elbow.
Sampling tube Elbow

Fig.4-17
Step 2:
Connect one end of the elbow to the Y-piece
Fig.4-18
53
Step 3:
Connect the other end of the elbow to the
breathing bag, or to patients through tube.
Fig.4-19
Step 4:
Connect the other end of the elbow to the
sampling tube, and make a connection
between the sampling tube and the CO2 or
anesthesia gas water trap.
Fig.4-20
4.2.6. AGSS Installation and Connection
CAUTION AP1000 cannot at an angle exceeding 5 degrees during normal operation.
CAUTION Make sure AP1000 installs at a place where operator can get a clear view of
it.
CAUTION Connect AP1000 according to the practical situation if no GCX rail is available
on the anesthetic machine.
CAUTION Make sure good connection in case of anesthesia gas leaks to operating
room.
54
Step 1:
Connect the transfer connector to the one connector of
the AGSS.
Fig.4-21
Step 2:
Connect two silica gel tubes to the connectors of the
transfer connector.
Fig.4-22
Step 3:
Connect the black connector of one silica gel tube to the

waste gas exhaust port on the bottom of the bellows
assembly.
Fig.4-23
Step 4:
Connect the black connector of the other silica gel tube
to the waste gas exhaust port on the breathing system.
Fig.4-25
55
4.3. Pre-operative Test
WARNING: For a full understanding of the performance characteristics of this equipment,
the user should carefully read this manual before operating
All system connections.

All WARNINGs and CAUTIONs.
How to use the machine.
How to test the machine.
WARNING: Do the following things before operating Aeon7200A
Finish all the tests listed in Pre-use Preparation.

Test other systematic parts.
WARNING: Do not use the machine if any test failures. Contact Aeonmeds authorized
service representative for maintaining the machine.
4.3.1. Test before Operation
Pre-use test should be performed under the following circumstances:
Every day before used on the first patient.

Before used on every patient.
After maintenance or service.
4.3.1.1. System Check
WARNING: Make sure that the breathing system is in good connection and with no
damage.
1. Make sure the anesthetic machine has no damage.

2. Make sure all parts are correctly connected.
3. Make sure the breathing system is correctly connected and has no damage; the
absorber canister is fully filled with soda lime.
4. Make sure the vaporizer is well locked and is filled with adequate anesthetic
agent.
56
5. Make sure the pipeline gas supply system is correctly connected and is at
proper pressure.
6. Make sure backup equipments are available and functioning.
7. Make sure anesthetic agent and emergent medicine are available.
8. Make sure the castors are not loose and the forefront two castors are locked.
9. Make sure the anesthetic machine is connected to power socket and power
indicator is light. There is no power supply if power indicator does not light.
4.3.1.2. Power Failure Alarm Test

1. Turn on power switch; user interface is light, STANDBY interface displays after
self-test is finished.
2. After the anesthetic machine operates under STANDBY mode for five minutes,
pull out power cord
3. Make sure power failure alarm occurs (alarm bell sounds or user interface
displays POWER FAILURE message).
4. Reconnect power cord.
5. Make sure alarm is eliminated.
4.3.2. Pipeline Gas Supply Test
CAUTION: Operator should make sure gas supplies are correctly connected during
operation; there is no leak, wrong connection and damage in breathing circuit. If something
abnormal occurs, check the connection.
WARNING: The malfunction of the center gas supply system may cause one or even all
connection equipment connected with it stopping work.
1. Cut off pipeline gas supply. Perform the following steps if pipeline gauge does
not read zero.
2. Connect O2 supply.
3. Set flow to the middle level.
4. Make sure N2O cylinder gauge reading restores to zero.
5. Cut off O2 supply.
6. Make sure O2 cylinder gauge reading restores to zero. Low gas source alarm
occurs when O2 pressure is decreasing
57
4.3.3. Vaporizer Test
CAUTION: For information of vaporizers function test, refer to VP300 User
Manual.(Material No.:130002374)
Make sure the vaporizer is steadily installed.

Make sure the vaporizer is locked.
Make sure only one vaporizer can be open at a time.
Make sure the vaporizer is filled with adequate anesthetic agent.
4.3.4. Alarm Test
1. Connect a test lung to Y-piece.

2. Turn on power switch.
3. Set the following items:
Ventilation Mode IPPV
Ventilator Vt700mL
Freq.20
I:E1:2
PAW-High40cmH2O
Anesthetic machine All gas flow: OFF
Push O2 flush to inflate bellows.
4. Make sure
Initiate mechanical ventilation.
No low gas source pressure alarm occurs.
Ventilator displays correct values.
Bellows moves up and down during mechanical ventilation.
5. Set O2 flow at 5L/min.
6. Make sure
End respiratory pressure is approximately between 2cmH2O to
3cmH2O.
58
Ventilator displays correct values.

Bellows moves up and down during mechanical ventilation.
7. Test O2 monitoring and alarm
Disassemble O2 sensor, make sure that O2 takes up 21% of room
air according to the test result.
Set low O2 alarm to 50%,make sure low O2 alarm occurs.
Set low O2 alarm to 21%, make sure low O2 alarm is eliminated.
Assemble O2 sensor in breathing system.
Set high O2 alarm to 50%.
Push O2 flush button to inflate bellows.
Make sure high O2 alarm is initiated.
Set high O2 alarm to 100%, make sure high O2 alarm is eliminated.
Put O2 sensor in pure oxygen; make sure that O2 takes up 100%
according to the test result.
8. Test low minute volume alarm
Return to alarm menu.
Set low minute volume alarm limit to 16.0L/min.
Make sure low minute volume alarm occurs.
Return to alarm menu.
Set low minute volume alarm limit to 10.0L/min, make sure low
minute volume alarm is eliminated.
9. Test high PAW alarm
Set high PAW below peak PAW.
Make sure high PAW alarm occurs.
Set high PAW alarm to 40cmH2O.
10. Test low PAW alarm
Disconnect test lung form breathing system.
Other alarms occur, such as low minute volume alarm.
Make sure low PAW alarm occurs.
11. Test continuous PAW alarm
Set control items
APL valve Adjust to the maximum value
Ventilation Mode Manual
Mechanical ventilation stops when the machine operates at Manual

ventilation mode.
59
Block patient end and push O2 flush button.

Make sure continuous PAW alarm occurs when continuous
pressure is at 10cmH2O for 15 seconds.
12. Turn off power switch.
60
5. Operating guide
5.1. Opening
Use the AC power, connect the pipeline gas resource and auxiliary gas resource and open the
auxiliary cylinder valve, close O2, N2O, Air flow meter and the auxiliary O2 flow meter.
Turn the switch to ON. The user

interface is lighted, entering into the
system self-test interface.
Fig. 5-1
5.2. System Self-test

Enter into the system self-test
interface after opening.
Follow instructions on the user
interface.
Select Skip to proceed to Manual
Test.
Fig. 5-2

interface.
Fig. 5-3
5.3. Automatic Leak Test

After System Self Test, the automatic
Test begins.
interface.
1) Select Continue to perform
Automatic Test.
2) Select Skip to proceed to
Manual Test.
Fig.5-4
1) Select Continue to perform
Automatic Test again.
2) Select Skip to proceed to Manual
Test.
Fig. 5-5
62
5.4. Manual Test

If the System test is not done before
performing the manual test, the user
interface of manual test will display
as the picture on the right.
Follow the instructions on the user

interface.
Select Skip, the system will enter
into normal interface.
Fig.5-6
If the Automatic test is not done
before performing the manual test, the
user interface of manual test will
display as the picture on the right.
Follow the instructions on the user

interface.
Select Skip, the system will enter
into normal interface.
Fig. 5-7
5.5. Patient Type Setting

The patient type of Aeon7200A anesthesia system has 2 types: Child and Adult. The user
can select the needed one.
CAUTION: Adult is the default patient type after opening.
CAUTION: The switch of the patient type is only allowed in STANDBY mode.
63
Adult is the default type after

opening.
Fig. 5-8
Press the knob to select patient
type button in the bottom, left
corner of the screen. This button
will turn yellow when selected.
Fig. 5-9
Turn the knob to change the patient
type to Child.
Fig. 5-10
64
Press the knob to confirm the

setting and un-select the patient
button.
Fig. 5-11
65
5.6. Ventilation Mode
IPPVIntermittent Positive Pressure Ventilation
PLVPressure Limited Ventilation
SIMVSynchronized Intermittent Mandatory Ventilation
PSPressure Support Ventilation
5.6.1.1. Intermittent Positive Pressure Ventilation(IPPV):
All the breathings are provided by the anesthesia machine, the patient cannot switch them by
self. The ventilation is managed by the predetermined ventilation volume, breathing frequency
and inspiration-expiration ratio to keep the tidal volume stable, thereby assure the stable MV.
The setup parameters of IPPV mode:
VT, Freq, I:E, Tp
5.6.1.2. Pressure Limited Ventilation(PLV):
The setup parameters of PCV mode:
PTARGET, Freq, I:E, TSLOPE, Plimit
5.6.1.3. Synchronized Intermittent Mandatory Ventilation (SIMV)

SIMV is a ventilation mode which combines spontaneous breathing with control ventilation.
Within the trigger window, the patient can trigger the command positive pressure ventilation
synchronizing with the spontaneous breathing. Between the two command ventilation cycle, the
patient is allowed to breathe spontaneously. The command breathing follows the presets
volume. By setting frequency and tidal volume to assure the minimum MV, cooperating with the
patients spontaneous breathing to reduce the rivalry between patient and machine and
negative effect of blood dynamics, and prevents the potential syndrome, such as air pressure
injury and so on.
By changing the presets frequency to change the breathing support level, in other words, from
entire support to partial support, the machine can be used for long-term patient to retreat from
machine.
The setup parameters of SIMV mode:
VT, Freq, Tins, Tp, Trigger
5.6.1.4. SPONT
The setup parameters of SIMV mode:
FreqMIN, Trigger,
67
5.6.2. Parameter and adjustment scope of ventilation mode
Patient Type Unit Range Default Stepping

Adult Valve
VT mL 201500 500 10 (Vt< 1000)

IPPV Mode 50 (Vt> 1000)
Freq. bpm 4 100 12 1
I:E / 4:1 1:8 1:2 0.5
TP % OFF, 5 60 10 5

Child Valve
IPPV Mode VT mL 20300 120 10

Freq. bpm 4 100 20 1
I:E / 4:1 1:8 1:2 0.5
TP % OFF, 5 60 10 5

Adult Valve
VT mL 201500 500 10 (Vt< 1000)

PLV Mode 50 (Vt> 1000)
Freq. bpm 4100 12 1
I:E / 4:1 1:8 1:2 0.5
Plimit cmH2O 570 20 1

Child Valve
PLV Mode VT mL 20300 120 10

Freq. bpm 4100 20 1
I:E / 4:1 1:8 1:2 0.5
Plimit cmH2O 570 10 1
68
Patient Type Stepping

Unit Range Default
Adult Valve
10 (Vt< 1000)
VT mL 201500 500
50 (Vt> 1000)
Freq. bpm 260 4 1
SIMV Mode TINSP sec 0.25.0 2.0 0.1
TP % OFF,560 10 5
Flow L/min 115 3 1

Trigger
Press cmH2O -200 -6 1
TSLOPE sec 02.0 0.5 0.1
Patient Type: Stepping

Unit Range Default
Child Valve
VT mL 20300 120 10
Freq. bpm 260 4 1
SIMV Mode TINSP sec 0.25.0 1.0 0.1
TP % OFF,560 10 5
Flow L/min 115 2 1

Trigger
TSLOPE sec 02.0 0.5 0.1
Patient Type Stepping

Unit Range Default
Adult Valve
SPONT Mode FreqMIN bpm 260 2 1
Flow L/min 115 3 1

Trigger
69
Patient Type: Stepping

Unit Range Default
Child Valve
FreqMIN bpm 260 4 1

SPONTMode
L/min 115 2 1
Trigger
cmH2O -200 -6 1
5.6.3. Ventilation Mode Setting

The user can select the ventilation mode according to the patients actual situation.
The ventilation mode menus locate on

the left corner of screen. Click on the
ventilation menu to select the
corresponding ventilation mode.
Fig. 5-11
If you wish to choose IPPV mode, click
the IPPV mode button. The button will
be at pre-selection state.
NOTE:
When the ventilation mode button is at
pre-selection state, the corresponding
ventilation parameters that can be set
appear on the bottom of the screen.
Fig. 5-12
70
Click the IPPV button again to confirm

your selection.
Fig. 5-13
5.6.4. Mode parameter setting

If the patient type and ventilation mode have been selected, the system will display default
parameters according to the ventilation mode. The user could set the needed breathing
parameter. VT of IPPV mode is used below as an example of how this is done. These
instructions also apply to other modes and parameters.
Click the parameter button to be set,

for example VT. The VT button will be at
pre-selection state.
Fig. 5-14
71
Turn the knob to adjust the

wanted parameter value.
Fig. 5-15
Click on VT button again the
setting.
Fig. 5-16
72
5.7. Menu screens
CAUTION: The menu window covers two waveforms.
CAUTION: When selected, a short cut key will display the selected menu. When Normal is
selected the all menus will be removed.
Menu screens are used to access most

functions in the anesthesia machine. All
menus open in specific menu windows.
Each menu opens or closes by touching
the screen or rotating the knob. Value
selection in the menu is accomplished
by touching the screen, rotating the
navigator knob and pressing the
navigator knob to confirm selection.
Fig. 5-17
5.7.1. Menu operating logic
1. Open / close current menu by pressing the corresponding touch key.

2. An open menu can also be closed by clicking on the "X" key or Normal" key.
3. Press the "Alarm" key to open / close the alarm setting menu. Press once to
open, and press again to close.
4. When the mode is in "pre-selection" status, closing or switching to another
menu will close pre-selection state.
5. If parameters are being set and not confirmed, the unconfirmed set values will
be lost and the original set values will be restored if the user closes the current
menu or switches to another menu.
73
5.7.2. Alarm setting

The alarm settings can be opened by touching the Alarm shortcut key. The alarm
setting menu includes four sub-options: Vent, Gas, Agent, and Volume. The default
alarm sub-option on start-up is Vent Alarm limits.
Vent:
Alarm limits for MV, PAW, Freq
can be set.
Fig. 5-18
Gas:
Alarm limits for FiO2etCO2
insCO2can be set.
Fig. 5-19
74
Agent:
Alarm limits for Sevoflurane (SEV),
Enflurane (ENF), and Isoflurane
(ISO) can be set.
Fig. 5-20
Volume: The alarm volume can be
adjusted.
Press the knob, the alarm volume

turns yellow as the right picture.
Turn the knob to set the needed
alarm volume and press the knob
to confirm you setting.
Fig.5-21
75
Log:
All the alarm messages can be
viewed from the log menu. Click on
the alarm message bar the detail
information of the corresponding
alarm appears on the screen.
Fig. 5-22
5.7.3. System setting

System setting menu includes nine
sub-menus: Pmean/Pplat, O2 sensor,
set time, system R/C, date format,
language, demo, trigger type and gas
module.
Fig. 5-23
76
Pressure: two options: Mean and Plat.

Language: two options: Chinese and
English.
Demo: two sections, including OFF
and ON.
Fig. 5-24
O2 Sensor: two sections, including
Enabled and Disabled.
Fig. 5-25
Set time:
Data: DD/MM/YY, YY/MM/DD,
MM/DD/YY
Time: 12 hour and 24 hour format.
Fig. 5-26
77
System R/C and date format
Fig. 5-27
Fig. 5-28
Language: two sections, including
Chinese and English.
Fig. 5-29
78
DEMO: enter the password 2020 to

open Demo mode.
Fig.5-30
Fig.5-31
Trigger: two options: Flow and
Pressure.
Note: Have this function in SOPNT and

SIMV mode.
Fig.5-32
79
Gas : three sections, including gas

module, co2 unit and wave form..
Fig.5-33
5.7.4. Calibration
The Calibration menu includes

O2Sensor, Gas Module, Leak Test,
Compliance, and Touch Screen.
Fig.5-34
5.7.4.1. Oxygen sensor calibration
CAUTIONRemove the oxygen sensor from the breathing system and expose
the sensor to room air for at least three minutes before proceeding.
Note: A plug is provided on a chain attached to the side of the breathing system for
plugging the O2 sensor port on the inspiratory valve during this operation.
80
CAUTION: The alarm O2 Cal Due will be displayed when the oxygen sensor has not been
calibrated for over 72 hours.
The oxygen sensor calibration

calibrates the oxygen sensor at 21%
oxygen concentration.
1. Press Oxygen button to enter the

Oxygen sensor calibration window
(see picture on the right).
Fig.5-35
2. The window displays a countdown
of 180s.
The Start button will be disabled

before the countdown ends.
1) After the countdown ends, select

Start button, the O2sensor calibration
begins.
2) Press , close the O2sensor

calibration.
If the O2sensor calibration succeeds

a word O2 sensor calibration
successful appears in the window.
Fig.5-36
If the O2 sensor calibration fails, a
word O2sensor calibration failed
appears in the window.
81
5.7.4.2. Gas Module

1. Press Gas Module button to enter
the Gas Module Calibration window
(see picture on the right).
Fig.5-37
2. Two notices appears, follow the
notice to operate.
The calibration of Gas Module result

will appears in the window.
Fig.5-38
82
5.7.4.3. Leak Test

Press Leak Test button to enter the
Leak Test calibration window (see
picture on the right).
Three notices appears, follow the
notice to operate.
Select Start to perform Leak Test
after completing the procedures on the
screen.
The calibration of Leak Test result will
Fig.5-39
CAUTION: Leak Test can only be performed in Standby mode.
NOTE: Perform the Leak Test prior to the Compliance Test when starting the system test.
5.7.4.4. Compliance
Press Compliance button to enter the

compliance calibration window (see
Three notices appears, follow the notice
to operate.
Select Start to perform Compliance
after completing the procedures on the
screen.
The calibration of Compliance result will
Fig.5-40
83
5.7.4.5. Touch screen calibration (If applicable)
Click on Touch screen sum-menu, the

screen seen as the right picture appears.
Fig.5-41
Press Start, the screen seen as the right
picture appears.
Click the + to complete the screen

calibration.
Fig.5-42
84
5.7.5. Service
Press Service button to enter the
Service setting interface (see picture on
the right).
Enter password 2010 and click on
, the interface shown as the

picture on the right.
Fig.5-43
The Service setting menu includes:
CAL IBRA., GAS STD.,
LANGUAGE, OPTIONS, ASSIST,
VERSION, TEST VAL and LOAD
DFT.
Fig.5-44
85
5.7.5.1. CALIBRA
The CAL IBRA sub-menu

includes: Press Sensor, Flow
Sensor, Inhale Valve (see
Fig.5-45
Pressure Sensor:
Press the Pressure Sensor knob to enter the Pressure Sensor Calibration, and
follow the intructions on screen to perform calibration.
1. Open the Y-piece

2. Turn off all flowmeters
3. Push the Start key
If the calibration successes, the interface will display Calibration Successed.
If the calibration fails, the interface will display Calibration Failed
Flow Sensor:
1Inspiration Sensor
Press the CAL IBRA-Flow Sensor-Inspiration Sensor key, the following prompt is
displayed:
1. Remove Insp. and Exp. valve disks, reinstall the valve covers;
2. Turn off all flowmeters;
3. Seal the Exp. Port;
4. Put the Supply through the throttle Valve, connect to the gas
inlet
5. Connect the flow monitor to the Insp. Port.
86
Perform the actions as instructed.
Press the button to finish the calibration.
2Expiration Sensor
Press the CAL IBRA Flow Sensor- Expiration Sensor , the following prompt is
displayed:
1. Remove Insp. and Exp. Valve disks, reinstall the valve covers;
3. Seal the Exp. Port;
4. Put the Supply through the throttle Valve, connect to the Exp.
Port.

Inspiration valve
Press the Inspiration valve key, the following prompt is displayed:

1. Remove Insp. and Exp. Valve disks, reinstall the valve covers;
3. Disconnect hoses from the Insp. Port and plug the Exp. Port;
4. Remove the Bellows, reinstall the Cover;
5. Select the Start key.
If the calibration successes, the interface will display Calibration Successed.
If the calibration fails, the interface will display Calibration Failed
87
5.7.5.2. GAS STD
The GAS STD. Sub-menu

includes: BTPS, ATP, STP (see
Fig.5-46
5.7.5.3. LANGUAGE
Select LANGUAGE sub-menu,
the interface shown as the
picture on the right appears.
Fig.5-46
88
5.7.5.4. OPTIONS
Select OPTIONS sub-menu, the

interface shown as the picture
on the right appears.
Fig.5-47
5.7.5.5. ASSIST
The Assist sub-menus include
Sensor Value and calibration
value.
Fig.5-48
89
Sensor Value includes:

Press Sensor, Flow Sensor,
Valve Sensor, O2 Sensor,
the detailed items are
shown on the right picture
Fig.5-49
Calibration Value includes:
Flow Valve, Insp. adaptor
Voltage, Exp. adaptor
Voltage, Standard
environment press, Current
environment press,
Pressure Zero vol..
Fig.5-50
90
5.7.5.6. Version
The Version includes: GUI,

BDU, KBD, PSU Version and
System ID.
Fig.5-51
5.7.5.7. TEST VAL
The TEST VAL includes result

of leak test.
Fig.5-52
5.7.5.8. LOAD DEF
91
The CAL IBRA sub-menu

includes: Press Sensor, Flow
Sensor, Inhale Valve (see
Fig.5-53
5.8. Breathing LoopFor Aeon7200A

Press the breathing loop button in the right side of the user interface, the breathing
loop appears in the user interface.
Save is in the low right of the circle to save the next circle as a reference circle.
When a loop is going or no circle displays, press Save to save the next entire
circle (inspiration and expiration) as a reference circle.
After pressing Save, Pressure-Volume circle and Flow-Volume circle are saved.
Press Save again and the system will cancel the current saved Pressure-Volume
and Flow-Volume reference circles at once and save two new reference circles.
When recede from the function circle window, the saved reference is stored.
CAUTIONWhen the STANDBY mode is set as work mode, the two saved
breathing circle will be canceled.
92
Fig.5-54 Pressure-Volume
Fig.5-55 Flow-Volume
93
Fig.5-56 Pressure-time waveform (Paw-t)
Fig.5-57 Velocity-time waveform (Flow-t)
Fig.5-58 Carbon dioxide-time waveform (CO2-t)
5.9. Closing
The shutdown of the anesthesia system is as follows:
Set the vaporizers to OFF;
Turn OFF the gas supplies, until the gas in the system has gone out completely;
Set all flowmeter settings to OFF;
Set the auxiliary flowmeter to OFF;
Turn the power switch to OFF to shut down the anesthesia system.
If disconnect the power supply, unplug the power cord.
CAUTION: When the power switch is processing OFF state, the main power is
still available.
WARNING: After closing the power switch, the system is running continually
until the background light of the flow meter has gone out.
94
6. Alarm and troubleshooting
WARNING: Person without maintaining experience mustnt mend the machine.
CAUTION: If alarm occurs, the patients safety must be protected firstly, then do
troubleshooting or necessary remedy.
CAUTION: Alarm presets will change with patient type automatically.
CAUTION: When several alarms occur at the same time, alarm message only displays the
front two in a sequence of High to Low.
CAUTION: When alarm silencing, the alarm bell has dashed X on itself. After
120s, the alarm bell renews to the old state; If the alarm is not dealt in time, alarm continues.
CAUTION: If alarm occurs when the anesthetic machine works normally, visible and
audible signals will delay a certain time.
WARNING: Do not set alarm limit exceeding the extremes, otherwise, alarm system will
failure.
WARNING: Potential hazard can exist if different alarm presets are used for the same or
similar equipment in any single area, such as ICU or cardio tic operating room.
WARNING: The operator should examine if the current alarm setting is suitable for every
patient.
WARNING: When power supply is interrupted, system will still renew the last alarm settings
when opening again.

6.1. Brief introduction of alarm message

The alarm states have 3 priorities: high, medium, low. High alarm needs to be dealt in time.
The sound pressure level of alarm signal is no less than 60dB.
The operator can judge if the alarm system is functional by visible and audible alarm message.
The distance that the operator can hear the alarm sound or distinguish the priority of alarm is 4
meters at least. And the distance to see the alarm message is not less than 1 meter at the front
of the machine.
The top area of the user interface displays alarm message, see figure 6-1.
Table 6-1 Alarm message
Table 6-1
Priority Definition Alarm Tone Mute Notice Message
High Death or 10 alarm tones 120s Red background, !!!flickering,

irreversible including 2hurry, displaying frequency is 2Hz.
injury. alarm cycle is 8s.
Medium Reversible 120s Yellow background, !! flickering,

injury. displaying frequency is 0.5Hz.
3 alarm tones,
alarm cycle is 10s.
Low Slight injury or 2 alarm tones, no 120s Yellow background, ! flickering,

uncomfortable. repeat. long-term display.
96
6.2. Alarm message

The alarm method includes technical alarm and functional alarm; technical alarm includes
startup test list and alarm occurring during normal operation.
6.2.1. Alarm default value and setting range
High Low Setting range of high limit Setting range of

low limit
MVAdult 12 1 125 020
MVChild 6 1
PAWAdult 50 10 1080 070
PAWChild 40 8
FreqAdult 18 --- 860 ---
FreqChild 30 ---
FiO2 100% 18% 21%100% 18%99%
Hal. 1.5 OFF 0.1%8.4% OFF, 0.1%8.3%
Iso. 2.3 OFF 0.1%8.4% OFF,
0.1%8.3%
Enf. 3.4 OFF 0.1%9.9% OFF,
0.1%9.8%
Sev. 4.2 OFF 0.1%9.9% OFF,
0.1%9.8%
Des. 12.0 OFF 0.1%21.9% OFF,
0.1%21.8%
ETCO2 6.6% OFF 0.1%9.9% OFF,
0.1%9.8%
50mmHg OFF 175mmHg OFF,
174mmHg
INSCO2 0.7% --- 0.11.4% ---
5mmHg --- 110 ---

Other default items
Manual Mode: Enabled
Alarm Volume: 2 tones
Patient type Adult
PressurePLAT
97
6.2.2. Technical alarm message table
Table 6-2
Alarm Name Priority Cause Remedy
Low gas supply High Drive gas pressure is less Check pipeline gas supply and
pressure than 2.9psi15% replace pipeline.
AC power Low AC power failure alarm Check connection, AC power

failure when AC power supply supply and fuse;
failure
Replace fuse when it is melt.
Low battery Medium No AC power and the Connect AC power supply

capacity battery voltage lower than immediately;
22V.
When the alarm appears, the
battery capacity can last 10
minutes.
Switch to the manual mode,

backup battery begins to supply
power and assure battery capacity
is full.
O2 sensor High Monitor O2 concentration

Use exterior measurement system
failure 10%, the alarm occurs
or replace O2 sensor.
immediately.
Monitor O2
concentration10%, cancel
the alarm immediately.
When O2 sensor in the

system setting menu is
configured Disable, no
alarm occurs.
98
BDU
High GUI receives and sends Ventilator failure.
communication
data from BDU unit failure
failure Switch to manual mode and the
lasts for 2s
user interface is still available.
User interface switches to
STANDBY mode automatically.
Call service Rep.
Flowmeter
High GUI receives or sends data Switch to manual mode
failure from flowmeter sensor
Call service Rep.
failure lasts for 2s
Communication
High Communication between Switch to manual mode and call
between BDU
BDU and power supply service Rep.
and power
board is abnormal.
supply board
failure
Gas module
High When gas module
communication
communication is
failure
abnormal, if the cable is
interrupted, this abnormal
state will last 5s.
Gas module High Pull out adapter probe in Call service Rep.
probe failure gas module for several
seconds.
CAUTION: If the gas
module communication
failures or interior error in
gas module, the alarm
message will not occur.
99
Interior error in High Any case of software, Call service Rep.

gas module hardware, electric
rotational speed exceeds
limit, no factory calibration
or factory calibration failure
appears, the alarm will
occur.
CAUTION: If the gas
failures, the alarm message
will not occur.
Gas module High When any parameter of the Call service Rep.
monitor detected CO2, N2O, O2,
concentration anesthetic gas exceeds
exceed limit limit, the alarm message
appears.
CAUTION: If the gas
failures or interior error in
gas module or gas module
probe is disabling, the
alarm message will not
appear.
Keyboard High No communication Switch to manual mode, Call

communication between UI and keyboard service Rep.
failure
100
6.2.3. Functional alarm message
Table 6-3
Alarm Name Priority Condition Solution Remedy
Continues high High 1. In MANUAL mode, airway 1. Use manual

airway pressure pressure>10cmH2O, and After alarm ventilation.
last more than 15s, this occurs, alarm 2.Check patients
alarm occurs; lasts at least expiratory passage
2. In other mode, airway for 8s. if the alarm is not
pressure>PEEP setting canceled, call
values, and last more service Rep.
than 15s, this alarm
occurs;
3. In STANDBY mode, this
alarm will not appear;
4. In MANUAL mode, this
alarm will not be closed.
High airway pressure High 1. Airway Ppeak Ppeak; 1.Switch to 1.Reset airway high
2. In STANDBY mode, this expiratory alarm limit;2.Detect
alarm will not appear; phase, the if expiratory
3. In MANUAL mode, this timer passage is blocked
alarm could be closed. 2. Alarm or not;
message lasts
3. If Vt setting is too
for 8s after
big; 4.If the patient
alarm
airway is blocked.
condition
disappears.
Negative pressure High 1. Airway pressureSW883 Do not block

-2cmH2O and lasts for SUCTION exhaust
more than 4s. port
In MANUAL mode, this alarm,
this alarm will not be closed.
101
APNEA High 1. Monitor tidal volume Alarm occurs.

<10ml, or
2. Monitor average
pressure<1cmH2O, in
MANUAL mode, it is not
determined, or
3. Monitor average pressure
equals to 1cmH2O, and
monitor PEEP0cmH2O,
in MANUAL mode, it is
not determined.
Low airway pressure Medium 1. In MANUAL mode, airway 1. Ventilator

pressure is lower than works as Reset airway low
pressure alarm low normal. alarm limit
limit>30s;
2. In other mode, Freq4;
airway pressure is lower
than alarm low limit>15s,
Freq<4, airway pressure
is lower than pressure
alarm low limit>30s;
3. In STANDBY mode, this
alarm will not appear
APNEA backup Medium SW425.2 in PS mode, Alarm occurs.

ventilation FreqMIN trigger ventilator.
Low FiO2 High 1. FiO2Low FiO2 setting 1. Alarm 1. Reduce alarm

occurs. setting;
2.Ventilator 2. Reduce air or
works as N2O compensation
normal. value; 3.Recalibrate
O2 sensor;
4.O2 battery is
exhausted;
5. Call service Rep.
102
High FiO2 Medium 1. Measured FiO2 value 1.Alarm 1.Increase FiO2 and
setting occurs. alarm setting
When O2 sensor 2.Ventilator
configuration in the system works as
menu is Disabled, this alarm normal.
will not appear.
High MV Medium 1. MV upper setting limit 1. Alarm 1.Increase high MV

In MANUAL mode, this alarm occurs. alarm limit;
could be closed. 2.Ventilator
works as
normal.
Low MV Medium 1. MV lower alarm limit 1.Alarm 1.Reduce MV alarm

In MANUAL mode, this alarm occurs. setting2.Check if
could be closed. 2.Ventilator there is leak in
works as patient end
normal.
High Freq Medium 1. MV HighFreq setting 1.Alarm 1.Check patients

2. The patient has occurs. state and if there is
spontaneous breathing. 2.Ventilator spontaneous
3. This alarm only applied to works as breathing;
PS mode. normal.(effecti
ve in PS
mode)
HighETCO2concentra High Expiratory CO2 concentration

tion exceeds high limit and lasts
at least 2 continual breathes
Low High ETCO2 concentration is

ETCO2concentration lower than low alarm limit and
lasts at least 2 continual
breaths.
HighINCO2 High Alarm according to detected

concentration real-time data
103
High PEEP Medium Detected PEEP exceeds

PEEP setting +5cmH2O for 2
breaths or 30s (choose the
minimum one between the
two).PEEP High alarm
occurs.
No this alarm
in STANDBY and MANUAL
mode.
Gas module When gas module Alarm occurs. Check connection or

communication failure High communication is abnormal, Alarm occurs. replace gas module
such as unconnected, and
lasts for 5s.
Gas module probe High Several seconds after pulling Alarm occurs. Check or replace
failure up adapter of gas module adapter
CAUTION: If the gas module
communication failures, this
message will not appear.
6.2.4. Self-test alarm

Table 6-4
Alarm Name Probable Cause Remedy
BDU EEPROM data fail Incorrect calibration in EEPROM Call service Rep.
check
EEPROM IC fail EEPROM cannot read/write Call service Rep.
PAW sensor fail The data of the PAW pressure Call service Rep.
sensor is incorrect.
Ambient pressure sensor The data of the ambient pressure Call service Rep.
fail sensor is incorrect.
104
PEEP valve fail Incorrect PEEP valve data Call service Rep.
Inspiratory valve fail Incorrect monitor sensor ZERO state Call service Rep.
Vent/Manual fail Incorrect valve state Call service Rep.
Flow sensor fail Incorrect sensor data Call service Rep.
SW version fail BDU, GUI, KBD software version is Call service Rep.
not the same with the released one.
BDU Comm. fail If GUI cannot receive and send data All breathing functions fail,
from BDU unit for 0.5s. call service Rep.
KBD Comm. fail No communication between GUI and All breathing functions fail,
Keyboard. call service Rep.
Inspiration valve fail Incorrect voltage value the inspiratory The machine can
valve feedbacks continue to work, but
there is only manual mode
but automatic mode, the
monitor function is
effective, call service Rep.
O2 supply fail The pressure of drive gas is lower Check if the pipeline
than 200kPa 15% . supply is normal, connect
the backup gas supply.
Alarm speaker fail Alarm speaker fails The ventilation machine

works as normal, the user
recedes or ignore, call
service Rep.
AC power fail AC power fails Check AC power supply,

check the fuse, replace it
when it is melt.
O2 sensor disconnect or O2 sensor fails or unconnected Replace O2 sensor or

fail connect O2 sensor; when
this alarm appears, the
105
setting of O2 sensor in the

system menu is disabled;
when there is no alarm,
the setting is Enabled.
Flowmeter fail
GUI receives or sends data from Switch to manual mode
flowmeter sensor failure lasts for 2s
Call service Rep.
6.3. Failure diagnosis

Table 6-5
No. Message Cause Remedy
1 O2 sensor The anesthetic gas 1. Use external gas measuring

failure measurement system has system.
failed
2.Call service Rep.
2 APNEA 1. Breathing or ventilation 1. Patient must immediately be

has stopped ventilated manually.
2. Check patients spontaneous

breathing ability.
3. Check ventilator settings.
4. Check fresh gas setting.
5. Check that everything is

connected.
6. Check hose system and tube.
3 Battery low The AC power failures and 1. Connect to main power.

the battery capacity of the
2. Check patients condition.
un-interruptible power
supply is almost 3. Prepare manual ventilation with
exhausted(20%).
106
100% O2.
4 APL valve 1. The connection or setting 1.Check APL valve connection

failures of APL valve is incorrect.
2.Select STANDBY mode and
return to the old ventilation mode;
3. Check APL valve setting.
5 High breathing 1. Breathing system is too 1.Check breathing system and

system high. breathing gas temperature;
temperature
6 Gas monitoring 1. Sample line is blocked or 1. Check sample line, water trap
has no unconnected. and Y-piece filter.
sampling signal
2. Replace if necessary.
7 Breathing 1.Incorrect connection of 1. Check tube, sample line and

system leaks pipeline or line filter.
8 Close AIR 1. Cylinder valve is open 1. Close cylinder valve to avoid

cylinder although central supply is unintentionally drawing gas from
available. the cylinder.
9 Close N2O 1. Cylinder valve is open 1. Close cylinder valve to avoid

10 Close O2 1. Cylinder valve is open 1. Close cylinder valve to avoid

11 CO2 sensor 1. CO2 gas measurement 1. Use external gas measuring

failure system has failed. system.
12 Continuous 1. The breathing pressure 1. Check ventilation and/or

107
high pressure exceeds the set limit for spontaneous breathing of the
more than 15s. patient.
2. Check breathing hoses,

breathing system, and gas
scavenging system for correct
functionality.
3. Check alarm limit for correct

setting.
13 ET CO2 high 1. The end-expiratory CO2 1. Check ventilation.

concentration has
exceeded the high alarm
limit for at least two breaths.
14 EXP. flow 1. Expiratory flow sensor 1. Replace flow sensor.

sensor failure has failed.
15 Fresh gas flow 1.Total fresh gas flow is 1. Reduce fresh gas flow;
too high above 19L/min.
2. Check vaporizer setting.
16 Fresh gas low 1. Fresh gas setting too low; 1.Increase fresh gad flow;
or leak
2. Leak. 2. Repair leak.
17 Gas sensor 1. Complete gas 1.Use external gas measuring

failure measurement system fails. system;
18. High airway 1. High alarm limit for the 1.Check hose system and tube;
pressure airway pressure has been
2. Correct the ventilation
exceeded;
settings.
2.Ventilation hose kinked;
3. Ventilation settings are

not correct.
108
19. Inaccurate 1. Reduced accuracy of 1.Reduce fresh gas flow fo reach

fresh gas flow fresh gas flow gas to below 12L/min;
measurement.
2. Check to take flow meter.
20. Inhaled CO2 1.Soda lime in circle system 1. Increase fresh gas flow;
high exhausted;
2.Replace breathing system;
2.Leak or fault in breathing
3.Adjust alarm limits if
system;
necessary;
3.High ventilation
4.Check ventilation settings;
frequencies;
5. Replace flow sensor.
4. Dead space ventilation.
21. Inspiratory flow 1. Inspiratory flow sensor is 1. Replace flow sensor.

sensor failure faulty.
22. Inhaled N2O 1. Inhaled N2O 1. Check N2O concentration in

concentration concentration exceeds the the fresh gas flow.
high high alarm limit of 82%.
23. Inhaled O2 1. Inhaled O2 concentration 1. Check O2 concentration in the

concentration exceeds the high alarm fresh gas flow.
high limit.
24. Inhaled O2 1. Inhaled O2 concentration 1. Check O2 concentration and

concentration is below the low alarm limit. fresh gas setting.
low
2.Check O2 supply;
3.Check breathing system and

breathing bag.
109
25. No air supply 1.Comm pressed air supply 1.Open optional backup air
has failed; supply;
2. Pipeline supply hose not 2.Check connection to piped

connected or kinked. medical air supply;
3.Optional air cylinder is 3.Connect a full air cylinder or

empty or closed; open the cylinder valve;
4. Compressed air 4. Check compressor.

compressor has failed.
26. No N2O supply 1.N2O supply has failed; 1. Open N2O backup cylinder;
2.Pipeline supply hose not 2.Check central gas supply and

connected or kinked; connection to central gas supply;
3. N2O cylinder empty or 3. Connect a full N2O cylinder or

closed. open the cylinder valve.
27. No O2 supply 1.O2 supply has failed; 1.Open O2 backup cylinder;
2.Pipeline supply hose not 2.Check central supply and

connected or kinked; connection to central supply;
3. O2 cylinder empty or 3. Connect a full O2 cylinder or

closed. open the cylinder valve.
28. O2cylinder 1. Pressure has dropped 1. Use a new O2 backup cylinder

pressure low below the pressure limit set and the central gas supply.
for the O2 cylinder.
29. O2flow 1. Fresh gas flow 1. Use only O2 as fresh gas and
measurement measurement for O2 has observe total flow meter.
failure failed.
30. PEEP high 1. Expiratory pressure 1. In automatic ventilation

5cmH2O above PEEP for 2 modes check the ventilation
breaths; or Expiratory parameters.
pressure 5cmH2O above
110
PEEP in pressure support 2. Check the anesthetic gas

mode for more than 30s. scavenging line.
31. Power failure 1. Power failure. 1.Restore central supply and

observe battery capacity;
2. Short-circuit in one of the
devices connected to an 2. Prepare manual ventilation.
auxiliary outlet.
32. Pressure 1. Pressure sensor faulty. 1.Perform self test;

sensor failure
33. Reinstall 1. Breathing system has 1.Check correct installation of

ventilator been installed incorrectly or breathing system;
in completely.
2. Breathing system 2. Check that upper diaphragm
defective. has been installed correctly.
3. Use a different breathing

system.
34. Setting can 1. The last setting has not 1. Repeat settings.
celled been accepted due to
2. Alarm can be reset by
temporary errors.
pressing Mute button.
35. Speaker failure 1. Speaker faulty. 1.No alarm tone;
36. Ventilator 1. Ventilator is no longer 1. Patient must immediately be

failure operational. ventilated manually.
2. Adequate substitute
monitoring must be ensured if
pressure and volume monitoring
has failed.
111
7. Cleaning and Disinfecting
WARNING: Use a cleaning and disinfecting schedule that conforms to your
institutions disinfection and risk-management policies.
Refer to the material safety data policy of each agent.
Refer to the operating and maintaining manual of all the disinfecting

equipments.
Wear safety gloves and safety goggles. The O2 sensor may leak and
burn (by Chlorine Potassium Oxide) if damaged. Do not inhale fumes.
Do not inhales fume.
CAUTION: To prevent damage:
Refer to the data supplied by the manufacturer if there are any

questions about the agent.
Never use any organic, halogenate or oil base solvent, anesthetic,

glass agent, acestone or other irritant agents.
Never use any abrasive agent to clean any of the components (i.e.
Steel wool, silver polish or agent).
Keep liquids far from the electrical components.
Prevent liquid from entering the equipment.
Do not immerse the synthetic rubber components more than 15

minutes: any longer will cause inflation, or accelerating aging.
Only the components marked 134 are pressure-resistant and

heat-resistant.
The PH value of the cleaning solution must be from 7.0 to 10.5.
WARNING: Talc, zinc stearate, calcium carbonate, or corn starch that has been
used to prevent tackiness could contaminate a patients lung or
esophagus, causing injury.
CAUTION: Never immerse the circuit O2 sensor or flow sensor connector in the
liquid.
Never dispose the circuit O2 sensor connector by using hot press.
Do not clean the inner surface of the flow sensor. Clean the outer
surface by using a damp cloth.
Check if there is damage in the components. Replace if necessary.
113
7.1. Cleaning and disinfection of pre-use first
Main unit Clean the machines panel and all surfaces with soft cloth soaked
with the water soluble disinfecting agent.
Sterilize main unit with ultraviolet radiation. Do not use acetic hyctro
peroxide or formaldehyde steaming.
Breathing system Refer to section 7.2

components
Absorber cycle Washing, refer to section 7.4
Bellows assembly Washing refer to section 7.5.3
7.2. Cleanable Breathing System Components
Corrugated tubing Corrugated tubing and reservoir bag used by every patient
(contacted with patient), should be cleaned then air the hydrocele in tube and reservoir
reservoir bag bag. Finally put the tube and reservoir bag into disinfector for
disinfecting or select disinfectant methods of rubber produces.
corrugated tubing and bag Washing to sterilize

(repetitious)
T-piece Washing to sterilize
Sampling probe and Clean with soap before use of each patient, and then washing
parallel lines of flow in disinfecting solution after airing.
114
7.3. Absorber
Refer to Disassembling the Absorber in the section 4.2.2
Changed color of the soda lime in the absorbent indicates that it has absorbed the carbon
dioxide; however, this color is not 100% accurate. To decide whether to replace the absorbent,
use CO2 monitoring machine.
Remove the changed-color absorbent immediately. The soda lime will restore its original color
several hours later and that may mislead the operator.
WARNING: The dry absorber may be very dangerous with the presence of any
anesthetic. Take proper measures to avoid dry soda lime in the

absorbent. Switch off all gas supplies after use.
115
7.3.1. Auto cleaning with agent or disinfector
Clean the absorber in the agent or disinfector according to the cleaning procedure.
Put the absorber in the heat-up room with the maximum temperature as 80or with the room
temperature.
Higher-level disinfection is recommended if the agent and disinfector cannot sterilize

equipment.
7.3.2. Manual cleaning
Rinse the absorber.
Immerse the absorber completely in the sink with water and agent about three minutes at a
temperature of 40 .
Rinse the absorber.
Higher-level disinfection must be performed after cleaning by hand.
7.3.3. Advanced Sterilizing
The absorber must be cleaned before advanced disinfecting.
The absorber can be placed in high temperature and high pressure conditions. The maximum
temperature recommended is 80.
Put the soda lime into the absorber after being dried, and then tighten the knob. Clear all soda
lime debris.
116
7.4. Breathing system
1. Inhalation valve and exhalation valve
Dismount the cover of the inspiration and expiratory valves by rotating it counter clockwise,
then clean all parts of them with the gauze soaked with water soluble disinfecting agent, after
all parts cleaned and dried recover it in original integration. Then one must check the leakage
and the movement of the inspiration and expiration valves in accordance with the required
regulation and checking procedure. Please handle all parts with care preventing any damage.
2. Breathing system module

Either vapouring (not more than 50) or immersion disinfection can be used in practice, in
case of immersion all sterilized parts must be dried with the high pressure air or oxygen before
reuse.
7.5. The Bellows Assembly
This section is about disassembling, assembling, cleaning and disinfecting the bellows
assembly. Read all content of this section before disassembling, assembling, cleaning and
disinfecting the bellows assembly to avoid equipment malfunction and patient injury.
CAUTION: Only folding gasbag is made of latex.
117
7.5.1. Disassembling
To disassemble the bellows assembly:
(To assemble the bellows assembly, perform the steps in Disassembling the bellows
assembly in reverse order):
1 Loosen the screws from the mounting plate, and then remove the mounting plate.
2 Turn counterclockwise and remove the bellows housing.
3 Detach the folding gasbag from the rim.
4 Detach the top plate from the folding gasbag.
5 Remove inner ring from the top of folding gasbag.
6 Push the locking spring to the center, and then remove the rim.
7 Remove the pressure-relief valve diaphragm and the seat assembly.
WARNING: Do not remove bellows assembly seat from diaphragm of the
pressure relief valve. This can distort the seat or diaphragm and
cause injury to the patient.
8 Push to the center, and then remove the locking spring.
9 Remove the seal
7.5.2. Testing Function
WARNING: Do not use any object small enough to slip completely into the
system when occluding the breathing system for test purposes.
WARNING: Always check the breathing system components for foreign
objects before using on a patient.
This test is to ensure all the components are installed correctly. It cannot replace the system
test. The bellows assembling can be installed in case they requirement testing. Otherwise, they
118
need to be disassembled to check and replace broken components, then reassembled and
tested.
Hold the bellows assembly in hands vertically upwards to occlude the driving gas port before
installing.
Invert the bellows assembly. If the descending velocity of the bellows top is no more than 100
ml/min, this could be because the driving gas port is not properly sealed, bellows or seal is not
installed correctly or other component are broken and that the descending velocity exceeds the
limit.
Open the driving gas port to make the bellows fully spread, and then occludes the breathing
system connector.
Turn the bellows assembly so it faces vertically upwards. If the descending velocity of the
bellows top is no more than 100 ml/min this could be because the bellows or pressure-relief
valve is not installed correctly or other component are broken and the descending velocity
exceeds the limit.
7.5.3. Cleaning and Sterilizing
Follow the machine and sterilizer manufacturers cleaning recommendations.
1. Cleaning
1) Disassembling.
WARNING: Never separate the diaphragm and the valve seat in a pressure-relief valve.
2) To prevent component damage, clean them lightly. Put the recommended non-enzyme mild
agent used for latex and plastic in hot water.
CAUTION: Do not immerse them more than 15 minutes to prevent inflation or aging.
3) Rinse using clean hot water, and then dry.
CAUTION: Dry by hanging while fully spread. If moisture is left in the bellows, they may
become tacky.
119
4) Check the components if they are broken or damp, then perform the assembling and
function test.
5) Connect the bellow assembly, ventilator and breathing system.
6) Perform the preoperative check.
2. Sterilizing
Cleaning and disinfecting must be performed at the same time. Follow instructions for the
common bellows assembly disinfection methods.
Sterilizing after general patient use:
Clean the inner and outer parts of the bellows assembly in a soap-and-water solution. Rinse
thoroughly in cold water, and dry with soft cloth. Immerse plastic and latex instruments in
70-80% ethyl alcohol for half an hour. Take them out using the aseptically transmits pliers, then
store in clean containers. Repeat this step before next use. Components made of metal and
glass can be sterilized with high pressure steam. When the steam pressure is increased by the
autoclave, the rising temperature can concrete the bacterium protein rapidly to kill bacteria. In
1.05 KG/CM2 steam pressure, the temperature rises to 121C. All bacteria and most sorus can
be killed if this temperature is maintained for 15-25 minutes.
Sterilizing after special infection or infectious patient use:
Open pulmonary TB, pulmonary abscess, pseudomonas, tetanus aeruginosa infection, gas
gangrene or infectious hepatitis is included. Used bellows assembly components must be
completely sterilized according to preliminary and final disposal procedures.
1) Preliminary disposal: Perform in accordance with the isolated disposal stipulation. Collect
and leave all the used bellows assembly components during the operation process in the
operating room. Immerse the bellows assembly components in the 1:1000 benzalkonium
bromide or 1-5% cresol for 30 minutes after finishing the operation.
2) Final disposal: perform the final disinfecting disposal after the bellows assembly components
are processed by the above-mentioned preliminary disposal:
Scrub the bellows assembly in a soap-and-water solution. Thoroughly rinse in cold

water, and dry;
If conditions permit, suffocating the components directly contacted with patients with
formald or oxirane is preferred, or perform immersing disinfection respectively. For
120
example: the components used by open pulmonary TB patients must be immersed in

3% cresol for 30 minutes; the components used by tetanus aeruginosa infection
patients must be immersed in 0.2% potassium permanganate for 30 minutes; the
components used by gas gangrene patients must be immersed in 0.1% chlorhexidine
for 30 minutes; the components used by pulmonary abscess patients must be
immersed in 0.1% benzalkonium bromide for 60 minutes; the components used by
pseudomonas patients must be immersed in 0.1% benzalkonium bromide for 120
minutes;
the components being immersed need to be rinsed by water and dried for next use;
scrub and rinse the components indirectly contacted with patients with 1-3% phenol
solution or soap-and-water solution and water. Irradiate them by using the ultraviolet
ray for 30 minutes if necessary.
121
7.5.4. Regular Maintenance
WARNING: Do not perform any tests and repairs when the equipment is being used to
avoid patient injury.
Perform the following check every 30 days to be sure that component worn by use and daily
cleaning are replaced in time.
Test by eyes
Separate the bellows assembly and anesthetic machine
Disassemble the bellows assembly
WARNING: Never separate the diaphragm and the valve seat in a pressure-relief
valve
Check each component carefully to check for cracks, distortion, dissolution, inflation and other
physical changes. Replace them if necessary.
Assemble the bellows assembly, and then perform the leak test.
122
8. User maintenance
WARNING: To prevent fire:
Please use admitted lubricant for anesthetic or O2 device.
Do not use lubricant containing oil or lipin, because when O2 concentration reaches a
certain degree, burning or explosion may happen.
WARNINGPlease observe disinfection control and safety regulation because the devices
having been used may contain blood and sap.
WARNING: Moving part and removable elements is in danger of jamming hands or crush.
More attention must be paid when moving or replacing system parts.
WARNING: In the process of removing product, strike and quiver must be avoided.
WARNING: Exhausted and old instruments (such as battery and LCD screen) harmful to
environment must be treated according to present local regulations.
Minimum maintaining Planned maintaining Standard

Standard
Daily Clean the outer surface.
weekly Perform 21% O2 sensor calibration.
Ventilate the system, open flow meter, and make sure that
the float move up and down smoothly. It can prevent
blocking and clinging.
monthly Perform 100% O2 sensor calibration.
Test leakage of bellows assembly. (refer to 7.5)
When cleaning and installing Check if any components are broken, and replace or repair
them if necessary.
As required Perform flow sensor calibration when flow waveform is

unusual.
Replace the filters in the gas inltet module (one year

generally).
Replace O2 sensor (one year generally).
8.1. General principle of maintenance

This chapter provides message needed by Aeon7200A anesthetic machine in term
maintenance. Replace or adjust some components before doing some calibration or
adjustment. If user uses improper components such as improper specification causes
malfunction, our company will not take responsibility. Do not use malfunction device.
Replacement and maintenance should be finished by authorized service engineer or qualified,
trained persons with repairmen experience. After maintenance, the device should be tested
and ensure its normal function and comply with the manufactures regulation. Use components
manufactured or sold by our company if replacement is needed, then test and ensure device
comply with the manufactures specification. If service support is needed, please call local
service engineer. In any case, the repairmen cost will include the current price and reasonable
personnel cost, but except repairmen items within Aeonmed companys warranty.
8.2. Maintenance schedule

Table 8-1
Action After each repair Every 12 months Every 36 months

Check before use X X X
Check before operation X X
Check with eyes X X
Replace exhausted X X
component
Replace O2 sensor
Replace/maintenance X
battery
Function test X X
124
CAUTION: Person without repair experience about such device must not repair this device.
CAUTION: According to this schedule to do maintenance timely and replace corresponding
parts.
CAUTION: The recommended repair time interval is 5 years. Breathing system, vaporizer
and parts are recommended to have a comprehensive test and replacement every 5 year.
8.2.1. Appearance checklist
1. Assure the appearance of Aeon7200A no damage, the anesthetic machine can run
normally.
2. Assure absorbent canister install correctly and fill enough soda lime. Assure enough
anesthetic in vaporizer.
3. Assure the exhaust gas absorber pipe connected with APL valve no damage and dry
inside.
4. Assure O2, N2O, AIR, VAC and EVAC connection pipe no damage.
5. Assure O2, N2O, AIR, VAC and EVAC flexible pipe no damage (if they are be used).
6. Assure AC power cable no damage.
125
8.3. Maintenance of O2 sensor
WARNING: Exhausted and old O2 sensor must be treated according to the present local
regulation. Not burn or dispose the O2 sensor casually.
CAUTION: Calibration of O2 sensor please refers to Chapter 5.5.4.1.
8.3.1. Replacement of O2 sensor
Replacement steps of O2 sensor:
1. Pull out O2 sensor from inspiratory valve of breathing system.
2. Pull out O2 sensor cable connection port from O2 sensor.
3. Connect new O2 sensor to cable connection port and install it on inspiratory valve of
breathing system.
8.3.2. Main technical parameter of O2 sensor
CAUTION: Specific parameters refer to the latest published technical data by manufacture.
O2 sensor can be used to detect partial O2 concentration of the anesthetic machine. O2 sensor
belongs to consumptive products, so attentions should be paid to its useful-life.and use as the
characteristics and technical requirements provided by manufacture. Main technical
requirements of O2 sensor in Aeon7200A as follows:
Performance parameters:
Maximum input range of interface: 0500mV DC
Interface form and definition: FCC-68 4 core telephone pin (RJ11-4), see the following
figure.
Output 9-13mV210mBar O2
Range 0-1500mBar O2
Signal 1001100% O2
Resolution 1mBar O2
Expected use life-span1.5x106% O2 hour(in 20 circumstance0.8x106% O2hourin

40circumstance
Total response timeT9015s
ZERO signalN2, +20200uV
Operations temperature range -20+50
Temperature compensationwithin 040 is 2%
Pressure range0.52.0Bar
Relative humidity range 099%no condensation
Long-term output excursion5%in 100% O2 circumstance and use more than one year
Crust MaterialWhite ABS
127
N2O resistance100% N2O
Valid time13 months
Complied standardEN12598/ISO7767
Suggested type and main characteristic parameters
128
8.4. Maintenance of fuse
WARNING: Disconnect AC power before fuse replacement, otherwise, it may cause injury
even death.
WARNING: When fuse replacement, fuse of the same type and size must be used,
otherwise, it can be harmful to the anesthetic machine.
CAUTION: Fuse belongs to damageable assembly, proper force must be used when
replacement.
CAUTIONUse screwdriver to swirl fuse and not use force largely and suddenly, otherwise,
it may cause fuse box broken.
Replacement steps:
Insert screwdriver into groove of the fuse box.
1. Rotate it about 45 counterclockwise, and then pull out fuse holder.

2. Take the fuse.
3. Install new fuse.
4. Pull new fuse to the original position.
5. Rotate it for about 45 with screwdriver clockwise to fix.
6. Connect AC power.
129
8.5. Battery Maintenance
CAUTION: Only service engineer authorized by our company can replace battery. If the
anesthetic machine is not used in a long time, please call service engineer to cut power supply
connection.
CAUTION: The exhausted and old battery must be treated according to present local
regulations.
Battery configuration
DC24V, 4AH, 12V leadacid battery, 2 nodes in series.
Use time8 hours and a half of an hour
CAUTIONS when use
Charging: when the AC power is connected, the system will charge the battery
automatically, the recommended charging time is no less than 8 hours.
Discharging: when the device uses battery to supply power, normally the work time is 120
minutes.
When the batterys electric capacity is insufficient, the device will display Low power
alarm until power off. When the Low power alarm occurs, the user should connect AC
power immediately and avoid the system closes (considering safety, manual startup
should be done to renew operation after the device closes automatically.)
Do not disassembly the battery causally and short battery connection line to avoid danger.
Batterys Preservation
If the battery is not used for a long time, it should be preserved after the battery is charged
fully.
When the preservation time exceeds 3 months, charge the battery at least every 3 months.
When preservation, humid and high temperature circumstances must be avoided.
Improper maintenance will cause battery broken, the battery should be replaced
immediately to avoid fluid leak erode device. Call manufacture when replace battery.
Battery removal
130
Use screw driver to remove the screws of the back cover board, disconnect the battery
module with device to remove battery.
8.6. Consumptive components replacement

Since installation, consumptive components names and code in every time dimension as the
table in below:
Consumptive components 6 months 12 months 48 months
Check /replace bellows assembly needless Check Replacement
Check /replace U sealed circuit needless Check Replacement
Check/replace AGSS transmission

needless Check Replacement
tube(optional)
Replace O2 sensor Check Replacement Replacement
131
9. Technical Data
CAUTION All technical specifications should be updated based on the real state of
Aeon7200A anesthetic machine; no notification will be made if any change happens.
CAUTIONAll display values are measured under dry environment and proper pressure.
WARNING Cylinder valve should be closed during pipeline gas supply, so that gas
shortage can be avoided due to exhausted gas supply or pipeline problems.
9.1. Pneumatic Diagram

Pneumatic system plays the role of supplying O2, N2O, AIR and anesthetic agent to breathing
system, ensuring their pressures are within normal range respectively, so that normal operation
of anesthetic machine and patients safety can be guaranteed.
Fig.9-1 Three Gas Supply Pneumatic DiagramV1.0
a: Main distinction, see chapter 10.2Table

133
1 Inlet filter 22 Safety valve

2 Pressure gauge 23 PEEP valve
3 Check valve 24 Ambient pressure
4 N2O Pressure regulator 25 Flow sensor
5 AIR Pressure regulator 26 Airway pressure
6 O2 Pressure regulator 27 Sensor board
7 Pressure sensor 28 AGSS
8 Pressure regulator 29 Exhaust valve
9 Pressure regulator 30 Pressure reversing valve
10 Auxiliary breathing O2 31 Bellows
11 Auxiliary supply O2 32 Reversing valve
12 ORC valve 33 APL valve
13 Flowmeter 34 Breathing bag
14 E-flowmeter 35 Flow sampling
15 O2 flush valve 36 Absorber container
16 Suction 37 O2 sensor
17 Check valve 38 Inspiration check valve
18 Vaporizer 39 Expiration check valve
19 Proportional solenoid valve 40 Ventilator
20 Solenoid valve 41 Breathing system
21 Throttle
134
9.2. System technical data
CAUTIONAll system gas supplies should be of medical degree.
Gas Supply
Table 9-1
Pipeline Gas O2, N2O, AIR

Pipeline Connection DISS-male, DISS-female, NISTISO 5359.
Connectors for each of the gas cannot be interchanged.
Pipeline Input Pressure 280-600kPa2.8-6bar
Flow Speed
Table 9-2
Gas Range Range

thin flow tube thick flow tube
O2 0.05-1L/min 1.1-10L/min
N2O 0.05-1L/min 1.1-10L/min
AIR 0.05-1L/min 1.1-12L/min
9.3. Electrical diagraph

Anesthesia machine can be divided into three parts: UI, drive control and circuit. UI consists of
computer system, auxiliary control circuit, power and etc, which mainly takes charge of display,
alarm, keyboard input and interface expansion. Drive control has BDU as its core. Exterior
sensor, signal processing, amplifier, power and battery are part of drive control which mainly
used for data acquisition and ventilation mode control. UI and drive control should be
connected by cables.
135
Fig.9-3 Electrical Diagraph
136
9.4. Physical data
CAUTIONAll physical specifications are of approximate values, no notice can be made if
any change happens.
CAUTIONDo not place Anesthetic machine in vibrant environment.
CAUTIONDo not put heavy stuff on the top panel or in the drawers.
Table 9-3
Dimensions 1403mm(H)681mm(W)855mm(D)
Weight 1105kgnot include vaporizer and
System
backup cylinder
Top Panel Load 25kg
Castor 125mm, each front castor with brake
Drawer 130mm(H)360mm(W)465mm(D)
Display 8 Touch Screen/ TFT Color Screen
Cylinder GaugeAIRO2 Range0-1MPa. Stepping0.05MPa

N2O
Accuracy2.5% of full range
Range-10 - 100cmH2O. Stepping200Pa

PAW Gauge
Accuracy2.5% of full range
Device lifetime:
8 years
137
9.5. Environmental requirement
CAUTIONThe anesthetic machine should be stored in draught room where there is no
caustic gas and storing magnetic field.
Table 9-4
Temperature Operation: 10~40
Storage: -20 ~ 55
Transport -20 ~ 55
Relative Humidity Operation: Not more than 80%, non-condensing.
Storage: Not more than 93%, non-condensing.
Transport Not more than 93%, non-condensing.
Operation: 70~106kPa
Atmospheric pressure
Storage: 70~106kPa
Transport 70~106kPa
Power AC100-240V, 50Hz/60Hz
Highest Attitude 3000m
138
9.5.1. IEC60601-1:2005 classification
Anesthesia machine belongs to this class:
Class I device
B type applied part
Common device/IP21
Mobile equipment
not use flammable anesthetic
Continuous operation
NOTE
The applied Part of anesthesia machine is the part between mask and Y-piece.
9.6. Input and output
NOTE:
1.When the anesthesia system stops transferring, the pipeline supplying pressure should be
280 to 600KPa.
2.When main power fails, the system switches to battery power automatically, and all the
anesthesia machine components can work normally.
3.When main power and internal battery both fails, the gas output is not affected.
139
9.6.1. Electrical
WARNING: IEC60601-1 is applicable to the connections between medical devices, and to
the connections between at least one medical device and one or more non-electrical devices.
Even if no functional connections between the single devices, when using one auxiliary power
outlet, they forms a medical electrical system. User must be aware of the risk of increased
leakage current and temperature and other increased risk may exist, when the device is
connected to the auxiliary socket-outlet.
WARNINGWhen earth wire has failure, if the device connects with auxiliary power supply,
it may cause patient current leakage exceeding the permitted range
WARNINGIf the exterior protective grounded wire has questions during wiring, interior
power supply must be used for device running.
Table 9-5
Supply Voltage 100-240VAC, 50/60Hz

Maximum Input Current 8A
AC power fuse F10AH 250VAC, 5X20F
Auxiliary AC power plug 4
Auxiliary AC power plug fuse T2AH 250VAC, 5X20T
Maximum output valve of auxiliary 1.5A(single plug)6A(in total)
AC power plug
Grounded resistance Small than 0.2
140
9.6.2. Pneumatic
Table 9-6
Pipeline supply O2AIRN2O

Pipeline connection DISS-male, DISS-female, NIST (ISO 5359)
All fittings used to connect O2, N2O and Air pipeline gas
supply are already.
APL valve 250kPa
Vaporizer connection 2 Selected interfaces
Pressure display Color mark list
Pipeline inlet pressure 280-600kPa
9.6.3. Electromagnetic compatibility
Changing or reassembling this equipment without authorization may cause electromagnetic

compatibility problems. Contact with Aeonmed for assistance. Designing and testing this
equipment is in accordance with the following stipulations.
WARNINGUsing cell phone or other radio radiant equipment near this product may cause
malfunction. Closely monitor the working condition of this equipment if

there is any radio radiant supply nearby.
Using other electrical equipment in this system or nearby may cause interference. Check if the
equipment works normally in these conditions before using on a patient.
Be careful of the following when Aeon7200A is connected:
Do not put any object which is not in accordance with EN60601-1 in the 1.5M range of patients.
An isolated transformer must be used for alternating current supply (in accordance with
IEC60989), or additional protective ground wires are equipped if all the devices (for medical or
non-medical use) are connected to Aeon7200A by using signal input/signal output cable.
If a portable all-purpose outlet is used as the alternating current supply, it must be in

accordance with EN60601-1-1 and cannot be put on the floor. Using another portable
all-purpose outlet is not recommended.
Do not connect the non-medical equipment directly to the alternating current outlet on the wall.
Only the alternating current supply of the isolated transformer can be used. Otherwise, the
141
surface leaking current may exceed the range permitted by EN60601-1 under the normal
conditions, and disoperation may cause injury to patients or operators.
Aeon7200A is equipped with all-purpose alternating current outlet for connecting other medical
equipment. Do not connect non-medical equipment to these outlets. Otherwise, the surface
leaking current may exceed the range permitted by EN60601-1 under normal conditions and
disoperation may be dangerous to patients or operators.
A complete system current leaking test (according to EN60601-1) must be performed after any
equipment is connected to these outlets.
WARNING The medical electrical equipment operators contact non-medical electrical
equipment and patients at the same time. It is dangerous for patients or

operators.
142
9.6.4. Guidance and manufactures declaration
Guidance and manufactures declaration electromagnetic emissions
-for all equipment and systems
Guidance and manufactures declaration electromagnetic emission
The Aeon7200A Anesthetic machine is intended for use in the electromagnetic environment
specified below. The customer of the user of the Aeon7200A Anesthetic machine should
assure that it is used in such and environment.
Emission test Compliance Electromagnetic environment guidance
RF emissions The Aeon7200 Aanesthetic machine uses RF

energy only for its internal function. Therefore, its
CISPR 11
Group 1 RF emissions are very low and are not likely to
cause any interference in nearby electronic
equipment.
RF emission The Aeon7200A Anesthetic machine is suitable

Class A for use in all establishments, other than domestic
CISPR 11
establishments and those directly connected to
Harmonic emissions the public low-voltage power supply network that
Class A supplies buildings used for domestic purposes.
IEC 61000-3-2
Voltage fluctuations/
flicker emissions Complies
IEC 61000-3-3
143
Guidance and manufactures declaration electromagnetic immunity
for all equipment and systems
specified below. The customer or the user of Aeon7200A Anesthetic machine should assure
that it is used in such an environment.
IEC 60601 test Electromagnetic

Immunity test Compliance level
level environment - guidance
Electrostatic 6 kV contact 6 kV contact Floors should be wood,

discharge (ESD) concrete or ceramic tile. If
8 kV air 8 kV air
floor are covered with
IEC 61000-4-2
synthetic material, the relative
humidity should be at least
30%.
Electrical fast 2 kV for power 2kV for power Mains power quality should
transient/burst supply lines supply lines be that of a typical
commercial or hospital
IEC 61000-4-4
environment.
Surge 1 kV differential 1 kV differential Mains power quality should

mode mode be that of a typical
IEC 61000-4-5
2 kV common 2 kV common
environment.
mode mode
Voltage dips, <5% UT <5% UT Mains power quality should

short interruptions be that of a typical
(>95% dip in UT) (>95% dip in UT)
and voltage commercial or hospital
variations on for 0.5 cycle for 0.5 cycle environment. It should be that
power supply the
input lines Aeon7200AAnestheticmachin
40% UT 40% UT e be powered from an

IEC 61000-4-11
uninterrupted power supply or
144
(60% dip in UT) (60% dip in UT) a battery.
for 5 cycles for 5 cycles
70% UT 70% UT
(30% dip in UT) (30% dip in UT)
for 25 cycles for 25 cycles
<5% UT <5% UT
(>95% dip in UT) (>95% dip in UT)
for 5 sec for 5 sec
Power frequency 3A/m 3A/m Power frequency magnetic

fields
(50/60Hz)
magnetic field Should be at levels
characteristic of a typical
IEC61000-4-8
location in a typical
environment.
NOTICE UT is the a.c. mains voltage prior to application of the test level.
145
for equipment and systems that are life-supporting
specified below. The customer or the user of Aeon7200A Anesthetic machine should assure
that it is used in such an environment.
Immunity IEC 60601 Compliance

Electromagnetic environment - guidance
test test level level
Portable and mobile RF communications

equipment should be used no closer to any part
of the Aeon7200A Anesthetic machine, including
cables, than the recommended separation
distance calculated from the equation applicable
to the frequency of the transmitter.
Recommended separation distance
3.5
d P
V1
Conducted
3Vrms 3 Vrms
RF
12
150 kHz to 80 d P
IEC V2
MHz
61000-4-6
outside ISM
bands a
12
10 Vrms d P 80 MHz to 800 MHz
E1
10 Vrms
23
d P 800 MHz to 2.5 GHz
150 kHz to 80 E1
MHz
Where P is the maximum output power rating of
146
in ISM bands 10 V/m the transmitter in watts (W) according to the

transmitter manufacturer and d is the
Radiated
recommended separation distance in metres
RF
10 V/m (m). b
IEC
80 MHz to 2.5 Field strengths from fixed RF transmitters, as
61000-4-3 c
GHz determined by an electromagnetic site survey,
should be less than the compliance level in each
frequency range.d
Interference may occur in the vicinity of

equipment marked with the following symbol:
NOTICE 1At 80 MHz and 800 MHz, the higher frequency range applies.
NOTICE 2These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.
a
The ISM(industrial, scientific and medical) bands between 150kHz and 80MHz are 6.765MHz
to 6.795MHz; 13.553 MHz to 14.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66 MHz to
40.70 MHz.
b
The compliance levels in the ISM frequency bands between 150kHz and 80MHz and in the
frequency range 80 MHz to 2.5GHz 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.
c
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 Aeon7200A
Anesthetic machine is used exceeds the applicable RF compliance level above, the
Aeon7200A Anesthetic machine should be observed to verify normal operation. If
abnormal performance is observed, additional measures may be necessary, such as
147
reorienting or relocating the Aeon7200A Anesthetic machine.
d
Over the frequency range 150 kHz to 80 MHz, field strengths should be less than 10 V/m.
9.6.5. Recommended separation distances
Recommended separation distances between portable and mobile
rf communications equipment and the equipment or system
for equipment or system that are not life-supporting
Recommended separation distances between
portable and mobile RF communications equipment and the Aeon7200A Anesthetic

machine
The Aeon7200A Anesthetic machine is intended for use in an electromagnetic environment in

which radiated RF disturbances are controlled. The customer or the user of the Aeon7200A
Anesthetic machine can help prevent electromagnetic interference by maintaining a minimum
distance between portable and mobile RF communications equipment (transmitters) and the
Aeon7200A Anesthetic machine as recommended below, according to the maximum output
power of the communications equipment.
Separation distance according to frequency of transmitter(m)
150 kHz to 80 150 kHz to 80 80 MHz to 800 800 MHz to 2.5

Rated
MHz MHz MHz GHz
maximum
output power outside ISM in ISM bands
12 23
of transmitter bands d P d P
E1 E1
12
(W) d P
3.5 V2
d P
V1
0.01 0.1167 0.1200 0.1200 0.2300
0.1 0.3689 0.3795 0.3795 0.7273
1 1.1667 1.2000 1.2000 2.3000
148
10 3.6893 3.7947 3.7947 7.2732
100 11.6667 12.0000 12.0000 23.0000
For transmitters rated at a maximum output power not listed above, the recommended
separation distance d in meters (m) can be estimated 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.
NOTICE 1 At 80 MHz and 800 MHz, the separation distance for the higher frequency range
applies.
NOTICE 2 The ISM(industrial, scientific and medical) bands between 150kHz and 80MHz are
6.765MHz to 6.795MHz; 13.553 MHz to 14.567 MHz; 26.957 MHz to 27.283 MHz; and 40.66
MHz to 40.70 MHz.
NOTICE 3 An additional factor of 10/3 is used in calculating the recommended separation

distance for transmitters in the ISM frequency bands between 150kHz 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.
NOTICE 4 These guidelines may not apply in all situations. Electromagnetic propagation is
affected by absorption and reflection from structures, objects and people.
149
9.6.6. Compliance correction
In all of software version, the anesthesia machine is able to carry out a compliance correction
which compensates for volume "lost" in hoses and in the breathing system.
The anesthesia machine determines the system compliance (hoses and breathing system) and
required later for compliance correction during the self-test or standby leak test. The hose of
standard equipped compliance has a fixed value of 11mL/kPa.
The VT set is delivered during the first breath.
P is calculated from end-expiratory pressure (P1) and end-inspiratory pressure (P2).
Csys: the system compliance.
Figure11-3 Pressure values
Having the system compliance (Csys) and P, Anesthesia machine can calculate which
volume (V) has been "consumed" by the system, or, in other words, which volume has not
been delivered to patient.
V = Csys x P
The anesthesia machine increases the volume to be delivered by the value V.
VTcorr = VT + V
The anesthesia machine repeats this procedure during each breathing phase so that the VT
delivered to the patient gradually approaches the set VT. This procedure is completed as soon
as the plateau value stops changing (0.5 cmH2O).The displayed flow and the resulting values
(for example, MV) are updated accordingly.
150
9.7. Anesthetic ventilator technical specifications
9.7.1. Anesthetic ventilator performance
Table 9-8
Maximum Inspiratory 80cmH2O

Pressure
Noise of the Whole Work normally(not including alarm), no more than 60dB(A)
Machine
Warm-up Time 5min
MV Max 20L/min
Inspiratory Flow Max 75L/min
Pressure Transmission 5-80cmH2O
Range
9.7.2. Ventilation parameter
Table 9-9
Item Range Steppin Default Value Remark

g
Vt 20-1500mL 10mL 120mL 20-100mL, error is 20mL
Child 100-1500mL, error is 20%
500mLAdult
Freq. -100, 1bpm 20bpm error is 1bpm or 5%,
2-100bpm(SIMV), Child choose the maximum one
2-60bpmSPONT 12bpmAdult
I:E 4:1-1:8 0.5 1:2 Have this function in IPPV,

PLV mode, error is 15%
TINSP 0.2-5.0s 0.1sec 1secChild Have this function in SIMV
2secAdult mode, error is 10% or 0.1s,
choose the maximum one
PEEP OFF, 0-30cmH2O 1cmH2 OFF Monitoring error is 2cmH2O
O or 20%, choose the
maximum one.
FreqMIN 2-60bpm 1bpm 4bpmChild Have this function in SPONT
151
2bpmAdult mode
TP OFF, 5%-60% 5% 10% Have this function in IPPV
SIMV mode, error is 30% of
the setting or 0.05s, choose
the maximum one
Trigger 1-15L/min 1L/min 2L/min Have this function in SIMV
Child SPONT mode , error is 20%
3L/minAdult or 1.3L/min, choose the
maximum one
Plimit 5-70cmH2O 1cmH2 10cmH2O(Child Have this function in PLV.
O ); 20cmH2O
152
9.7.3. Gas dynamics
Table 9-10
Gas source Anesthetic system

Gas component O2
Rating supply pressure 400kPa
Inlet pressure range 280kPa ~ 600kPa
Flow valve range 5~75L/min
1
Output Pressure range: 0 ~ 8kPaFlow range: 0 ~ 75L/min
Label 1Within rated outlet pressure range and under double maximum rated inlet pressure condition.
Table 9-11
According to ISO8835-2, test under peak flow 60L/min, fresh gas 10L/min.
Item Standard Requirment Test Result

Expiratory impedence <0.6kPa 0.51
under manual condition
Inpiratory impedence <0.6kPa 0.39

under manual condition
Expiratory impedence <0.6kPa 0.57

under automatic condition
Inpiratory impedence <0.6kPa 0.22

under automatic condition
9.7.4. Monitor performance
Table 9-12
Item Range Stepping Accuracy

Vt 0 - 3000mL 1mL 20-100mL, error is 20mL
100-3000mL, error is 20%
Freq. 0 - 110bpm 1bpm 1bpm
PEAK -20 - 99cmH2O 1cmH2O 5%, at least1cmH2O
MEAN -20 - 99cmH2O 1cmH2O 5%, at least1cmH2O
PLAT -20 - 99cmH2O 1cmH2O 5%, at least1cmH2O
FiO2 18 - 100 1% Error is 3 concentration
value
C 0-100mL/cmH2O 1mL/cmH2O Error is 20% or 5mL/ cmH2O,
0-99 mL/cmH2O choose the maximum one
7600A
PEEP -20 - 99cmH2O 1cmH2O 2cmH2O
PAW -20-99cmH2O 1cmH2O Error is3cmH2O or 10%,
choose the maximum one
100%, 75%, 50%, 25%, 0%
When battery is used to supply power, this sign displays available
Battery voltage state
remaining electric voltage.
display
When the vehicle is connected with AC power, this sign means
charging.
Pressure monitor range: 0 - 80cmH2O.According to different airway
pressure, gain the wave form displays is different.
0 ~ 10cmH2O, pressure axis gain 5cmH2O
Paw-t wave form 0 ~30cmH2O, pressure axis gain 10cmH2O
0 ~80cmH2O, pressure axis gain 20cmH2O
Time axis is a fixed range.the axises of Flow-t, Paw-t is same.
When gas module is opened, 0 ~15sGas module is closed, 0 ~20s.
Display range of flow rate: -90 - 90L/min, gain :45L/min. On time axis,
the positive axes stands for inspiratory direction; under the time axis,
Flow-t Wave form
the negative axes stands for expiratory direction. Flow rate is 0L/min,
which means no gas flow rate in airway.
CO2 display range is 0 - 76mmHg, gain is 38mmHg
CO2 time wave form Time axis is a fixed range.
When gas module is opened, 0 ~15sGas module is closed, 0 ~20s.
P/V Loop Horizontal abscissa displays Pawfixed range :-20~ 80cmH2O, gain
154
is 20cmH2O
Vertical abscissa displays tidal Volumefixed range is 0~ 1500ml, gain
is 250ml.
Horizontal abscissa displays tidal Volume -1400 ~ 0mL, gain is
700mL.
F/V Loop Vertical abscissa stands for Flowfixed range -90 - 90L/min, gain is
45L/min The positive axes stands for aspiratory flow rate, the
negative axes stands for expiratory flow.
9.8. O2 sensor specification

Table 9-13
Response time No more than 15s.

Sensor type Chemical fuel battery
Antipated battery Normal operation period is 12 months.
life-span
O2 monitor monitors and displays O2 concentration in the patient
loop. O2 sensor accessory includes one O2 sensor. This sensor can
produce a voltage proportional with O2 partial pressure in its detected
surface and its metal electrode will exhaust gradually in the process
of oxidation.
O2 sensor is an electrochemical appliance (chemical battery). O2

diffuses into this device by penetrating a membrane to make the
metallic electrode oxidizing. In this process, electric current occurs,
Operating principle of which matches with partial pressure of oxygen displayed by electrode
O2 monitor sensor.
The sensors voltage is influenced by the temperature of monitoring

gas blender. The thermostat outside of the sensor can compensate
the temperature change in sensor.
O2 monitor uses signal to deal and analyze circuit, transforming the

sensor signal to corresponding oxygen percentage value.
The system displays this value and compares it with the saved alarm
extremes. If this value exceeds the extremes, the monitor will send
alarm.
155
9.9. Gas monitoring module technical specifications

The gas monitoring module is used to connect other medical devices, provide monitor data,
monitor and display CO2, N2O and 5 anaesthetic gases (halothane, isoflurane, enflurane,
sevoflurane, desflurane).
The gas monitoring module is connected to the patients breathing pipeline to monitor the
inspiratory and expiratory gas and can be applied to Adult/Child and Infant.
CAUTION: Gas monitoring module complies with ISO 80601-2-55:2011.
9.9.1. MAC calculation of IRMA/ISA gas analyzer
Algorithms used in the host monitor to determine MAC values
Minimum alveolar concentration (MAC) is a standard for comparing the potency of inhalation
anesthetics. The MAC value represents the alveolar concentration of an anesthetic (at one
atmosphere) that, in 50 percent of a tested population, prevents gross muscular movement in
response to a painful, standardized stimulus.
If a mechanism to determine MAC values is implemented in the host device, the algorithms
used for this calculation must be adequately documented.
The MAC value may be calculated and displayed by using end-tidal (Et) gas concentrations
according to the following formula:
156
9.9.2. Mainstream gas monitoring module
Table 9-14
IRMA CO2 / AX+

Model
Interface type RS232, 9600bps
Accessories Airway adapter, disposable.
Working principle of The gas module is a mainstream gas monitoring module, connecting
gas module to patient to monitor gas concentration of breath.
The gas module can be used for adults, children and infants.
The gas module uses infrared technology, which determines gas

concentrations by measuring different wavelengths according to
different absorption of gases to different ray.
Table 9-15
Basic Configuration
Description Extremely compact infrared mainstream multi-gas module.
Available in various parameter configurations.
Dimension(WDH) IRMA CO2/ AX+:
383734mm(1.491.45 1.34)
Cable length 2.50m0.1m
Weight <25g(except cable)
Operating temperature IRMA CO2: 0-40, 32-104
IRMA AX+: 10-40, 50-104
Storage and IRMA CO2: -40-75, -40-167

transportation
IRMA AX+: -20-75, -4-167
temperature
Operating humidity <40hPa H2O(non-condensing)(95%RH at 30 degree celsius)
Storage and 5-100%RH, condensation1)

transportation humidity
Operating atmospheric 525-1200hPa(525 hPa corresponding to an altitude of

pressure 4572m/15000feet)
Storage and 500-1200hPa

transportation pressure
Mechanical strength Withstands Repeated 1.8m drops on a hard surface.
Complies with requirements for road ambulances according to

prEN1789 (clause 6.4) and requirements for shock and vibration
according to ISO 80601-2-55:2011 (clause 201.15.3.5.101,
transport).
158
Power supply IRMA CO2:
4.5-5.5VDC, Max 1.0W
(power on surge @ 5V less than 350mA during 200ms)
IRMA AX+:
4.5-5.5VDC, Max1.4W
(power on surge @ 5V less than 350mA during 200ms)
Surface temperature (at IRMA CO2:

ambient temperature
Max 39 degree C/102FIRMA AX+:
23)
Max 46 degree C/115F
Interface Modified RS-232 serial interface operating at 9600bps
Airway adapter Disposable adult/child:
Adds less than 6mL deadspace;
Pressure drop less than 0.3cmH2O @ 30LPM.
Disposable infant:
Adds less than 1mL deadspace;
Pressure drop less than 1.3cmH2O @ 10LPM.
NOTE 1: After being in a condensing atmosphere, this module shall be stored for more than
24 hours in an environment equivalent to operating humidity.
The humidity range 50-100% is valid for the temperature range -40 - 40.
Table 9-16
Data Output
Fiand ET The newest breathing value (Fi and ET) is continually displayed after
one breath.
Gas monitor module CO2CO2
159
Automatic agent IRMA AX+: Primary and secondary agent.

identification
Table 9-17
Gas Analyzer
Probe 2-9 channel NDIR type gas analyzer measuring at 4-10 m. Pressure,
temperature and full spectral interference correction.
Warm-up Time IRMA CO2: <10 seconds (full accuracy)

IRMA AX+:<20 seconds (agent identification enabled and full
accuracy)
Rise time CO290ms
(@10L/min)
N2O300ms
HAL, ISO, ENF, SEV, DES300ms
Agent identification <20s (Typically<10s)

time
Total system <1s

response time
Table 9-18
Accuracy specifications - standard conditions: The following accuracy specification is

valid for dry single gas at 22+/-5 degree C and 1013+/-40hPa.
Range1)
Gas CO2 AX+ Accuracy
CO2 0-15 0-10 (0.2vol%+2% of reading)
10-15 (0.2vol%+2% of reading)
15-25 15-25 Unspecified
N2O -- 0-100 (2vol%+2% of reading)
160
HAL, ISO, ENF -- 0-8 (0.15vol%+5% of reading)
8-12
SEV -- 0-10 (0.15vol%+5% of reading)
10-15
DES -- 0-22 (0.15vol%+5% of reading)
22-25
NOTE 1: Gas concentration reported in units of volume percent.
Table 9-19
Accuracy specifications all conditions1)
Gas Accuracy
CO2 (0.3vol%+4% of reading)
N2O (2vol%+5% of reading)
Agents2) (0.2vol%+10% of reading)
NOTE 1: The accuracy specification is valid for the operating temperature and humidity
conditions specified, except for interference specified in the table Interfering gas and vapor
effects below and the section "effect from water vapor partial pressure on gas reading". The
effect from water vapor partial pressure on gas reading.
NOTE 2: The accuracy specification for IRMA AX+ is not valid if more than two agents are
present in the gas mixture.
Table 9-20
Interference gas and vapor effects
Gas or vapor Gas CO2 Agents N2O

level
IRMA CO2 IRMA AX+
161
N2O3) 60 vol% --1) --1) --1) --1)
HAL3) 4vol% --1) --1) --1) --1)
ENF, ISO, SEV3) 5vol% +8% of reading2) --1) --1) --1)
DES3) 15vol% +12% of reading2) --1) --1) --1)
Xe(Xenon) 3) 80vol% -10% of reading2) --1) --1) --1)
Xe(Helium) 3) 50vol% -6% of reading2) --1) --1) --1)
Metered dose Not for use with metered dose inhaler propellants
inhaler
propellants3)
C2H5OH(Ethanol) 3) 0.3vol% --1) --1) --1) --1)
C3H7OH(Isopropan 0.5 vol% --1) --1) --1) --1)

ol) 3)
CH3COCH3(Aceton 1 vol% --1) --1) --1) --1)

e) 3)
CH4(Methane) 3) 3 vol% --1) --1) --1) --1)
CO(Carbon 1 vol% --1) --1) --1) --1)

monoxide) 3)
NO(Nitrogen 0.02 vol% --1) --1) --1) --1)

monoxide)3)
O23) 100 vol% --1) --1) --1) --1)
NOTE 1: Negligible interference, effect included in the specification Accuracy, all
conditions above.
NOTE 2: Interference at indicated gas level. For example, 50vol% helium typically
decreases the CO2 readings by 6%. This means that if measuring on a mixture containing
5.0vol% CO2 and 50vol% helium, the measured CO2 concentration will typically be
(1-0.06)*5.0vol%=4.7 vol% CO2.
162
NOTE 3: According to the ISO 80601-2-55:2011.
163
9.9.3. Sidetream gas monitoring module
Table 9-21
ISA CO2 / AX+

Model
Interface type RS232, 9600bps
Accessories Sampling tube, CO2oranesthetic gas Water trap, disposable.
Working principle of The gas module is a sidestream gas monitoring module, connecting
gas module to patient to monitor gas concentration of breath by electrical
machine inhaling trace gas.
The gas module can be used for adults, children and infants.
The gas module uses infrared technology, which determines gas

concentrations by measuring 10 different wavelengths according to
different absorption of gases to different ray.
164
Table 9-22
Basic Configuration
Description Ultra-compact, low-flow sidestream gas analyzers with integrated

pump, zeroing valve and flow controller.
Dimension(WDH) ISA CO2/ AX+:
236238mm(0.92.4 1.5)
Weight 75g
Operating temprature ISA CO2: 0-50, 32-122
ISA AX+: 5-50, 41-122
Storage and -40-70, -40-158

transportation
temperature
Operating humidity 4kPa H2O(no condensation)
(95%RH at 30)
Storage and 5-100%RH(condensation)1)

transportation humidity
(100%RH at 40)
Operating atmospheric 52.5-120kPa(corresponding to a max altitude of 5211m/17100feet)

pressure
Storage and 20-120 kPa (corresponding to a max altitude of 11760m/38600feet)

transportation pressure
Ambient CO2 800ppm
Mechanical strength ISA CO2:
Meets the shock and vibration requirements for transport of ISO

80601-2-55:2011 (clause 201.15.3.5.101.2) and EN 1789-2007
(clause6.3.4.2).
165
ISA OR+/AX+:
Meets the shock and vibration requirements for transport of ISO

80601-2-55:2011 (clause 201.15.3.5.101.1)
Power supply 4.5-5.5VDC,
ISA CO2: 1.4W(normal op.), 1.8W(peak @5VDC
ISA AX+: 1.6W(normal op.), 2.0W(peak @5VDC
Interface Modified RS-232 serial interface.
Software upgrade possible using the RS-232 serial interface.
Water handling Nomoline Family sampling line with proprietrary water removal
tubing.
Sampling flow rate 5010mL/min
NOTE 1: After condensation, the unit shall be stored for more than 24 hours in an
environment with relative moisture content below 95%RH (non-condensing).
Table 9-23
Data Output
Fiand ET3 Fiand ET are displayed after one breath and have a continuously
updated breath average.
ET will typically decrease below nominal value (ETnom) when

respiration rate (RR) exceeds the RR threshold (RRth) according to the
following formulas:
ET=ETnom(125/RR) for RRth>125
N2O, O2, DES, ENF, ISO, SEV
HAL
166
Automatic agent ISA OR+/AX+: Primary and secondary agent.

identification
Table 9-24
Gas Analyzer
Sensor head 2-9 channel NDIR type gas analyzer measuring at 4-10 m.
Calibration No span calibration is required for the IR bench. An automatic zero

reference calibration is performed at startup and then every 24 hours1.
Warm-up Time ISA CO2: <10s(concentrations reported and full accuracy)
ISA AX+: <20s(concentrations reported, automatic agent identification

enabled and full accuracy)
Rise time 200 ms

(@10L/min)
300 ms
N2O, O2, ENF, ISO , SEV, DES 400 ms
HAL 500 ms
Agent identification <20s (typically<10s)

time
Total system <3s(with 2m sampling line)

response time
Table 9-25
The following accuracy specifications are valid for dry, single gases at 225 and 101340
hPa.
Accuracy specifications - standard conditions
Gas Range Accuracy
CO2 0-15% (0.2vol%+2% of reading)
15-25% Unspecified
167
N2O 0-100% (2vol%+2% of reading)
HAL, ISO, ENF 0-8 % (0.15vol%+5% of reading)
8-25% Unspecified
SEV 0-10% (0.15vol%+5% of reading)

Unspecified
10-25%
DES 0-22% (0.15vol%+5% of reading)

Unspecified
22-25%
Table 9-26
Accuracy specifications all conditions
Gas Accuracy
CO2 (0.3vol%+4% of reading)
N2O (2vol%+5% of reading)
Agents1) (0.2vol%+10% of reading)
NOTE 1: The accuracy specification is not valid if more than two agents are present in the
gas mixture. If more than two agents are present, an alarm will be set.
Table 9-27
Interference gas and vapor effects
Gas or vapor Gas CO2 Agents N2O

level
ISA CO2 ISA AX+
N2O4) 60 vol% --2) --1) --1) --1)
HAL4) 4vol% --1) --1) --1) --1)
ENF, ISO, SEV4) 5vol% +8% of reading3) --1) --1) --1)
DES4) 15vol% +12% of reading3) --1) --1) --1)
168
Xe(Xenon) 4) 80vol% -10% of reading3) --1) --1) --1)
Xe(Helium) 4) 50vol% -6% of reading3) --1) --1) --1)
Metered dose Not for use with metered dose inhaler propellants
inhaler
propellants4)
C2H5OH(Ethanol) 4) 0.3vol% --1) --1) --1) --1)
C3H7OH(Isopropan 0.5 vol% --1) --1) --1) --1)

ol) 4)
CH3COCH3(Aceton 1 vol% --1) --1) --1) --1)

e) 4)
CH4(Methane) 4) 3 vol% --1) --1) --1) --1)
CO(Carbon 1 vol% --1) --1) --1) --1)

monoxide) 4)
NO(Nitrogen 0.02 vol% --1) --1) --1) --1)

monoxide)4)
O24) 100 vol% --1) --1) --1) --1)
NOTE 1: Negligible interference, effect included in the specification Accuracy, all
conditions above.
NOTE 2: Negligible interference with N2O/O2 concentrations correctly set, effect included in
the specification Accuracyspecifications- all conditions above.
NOTE 3: Interference at indicated gas level. For example, 50vol% helium typically
decreases the CO2 readings by 6%. This means that if measuring on a mixture containing
5.0vol% CO2 and 50vol% helium, the measured CO2 concentration will typically be
(1-0.06)*5.0vol%=4.7 vol% CO2.
NOTE 4: According to the ISO 80601-2-55:2011.
169
10. Appendix
10.1. Accessories List
No. Part No. Name Specification

1. 122002919 AGSS AP1000
2. 122000048 O2 Pipeline white M221.5 , 11.5 connecter
3. 122000049 N2O Pipelineblue M221.5 , 9.5 connecter
4. 122000050 Air Pipelineblack M221.5 , 9 connecter
5. 122001476 Auxiliary O2 pipeline M141.5, 10 connecter
6. 122002613 Adult PVC Breathing Circuit package
7. 230000311 FACE MASK(PVC) XL(4#)
8. 230000312 Anesthesia Breathing Circuit ADULT
9. 230000075 Bag3L 3L
10. 230000076 Breathing Bag2L 2L
11. 121000065 Adult Silicon Breathing Circuit package
12. 230000538 Adult Silicon Hose package l=1000mm, 22
13. 230000163 Adult Silicon FACE MASK PN-0007AM(4#)
14. 230000113 Elbow Male and female cone 22
15. 230000101 Y Piece 22, 15cone
16. 130000798 Straight connector 22 male cone
17. 240000415 IRMA_CO2 module IRMA CO2
18. 240000414 IRMA_AX+ gas module IRMA_AX+
19. 210001975 O2 sensor MOX-4
20. 122000831 Wean PVC Breathing Circuit package
21. 240000028 WeanAnesthesia Breathing Wean
22. 122003285 Wean
Circuit Silicon Breathing Circuit package
23. 230000066 FACE MASK ( PVC) HX.O11 M(2#)
24. 230000539 Wean Silicon Hose package l=1000mm, 15
170
10.2. Table
Gas Supply O2N2OAIR O2N2O O2
Flow-meter Double Tube Flow-meter 4 Tubes Flow-meter 6 Tubes Flow-meter
Vaporizer Manifold Double Vaporizer Single Vaporizer
171
This manual No.: 130014266
CE mark in this manual apply only to

product with CE mark.
Directive 93/42/EEC
concerning Medical
Devices
Beijing Aeonmed Co., Ltd.

Tel: +8610-83681616
Fax: +8610-63718989
E-Mail: service@aeonmed.com
Website: http://www.aeonmed.com
Edition 00.00
Mar. 2016

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Aeon7200A Series User Manual

Beijing Aeonmed Co., Ltd.

Everything written in this manual is considered to be correct. Aeonmed is not legally

Installation, adjustments, mending and repairs must be performed by individuals

CAUTION: This equipment is not for home use.

The paid theoretical framework diagram will be supplied according to customer

Manufacturing techniques and materials:

Machines without maintenance or machines broken

The label of our original serial number or mark is removed or replaced

Other manufacturers product.

The assemblies are disassembled, extended and readjusted

1. Obtain the rights of return

Registered Address: 11B2, Fengtai Science Park, Beijing, PEOPLESREPUBLIC OF

European Shanghai International Holding Corp. GmbH(Europ)

Production No.10, Chaobai St., Yanjiao Development Zone, Sanhe, Hebei

Web site: Http://www.aeonmed.com/

Service Hotline 800-810-8333

1.1. General Information .......................................................................................................................... 1

2.1. Configuration ................................................................................................................................... 16

3. User Interface .......................................................................................................................................... 33

3.1.1. Main Interface Display ............................................................................................................ 35

4.1. Installation and Connection ............................................................................................................. 47

5. Operating guide ....................................................................................................................................... 61

5.1. Opening ........................................................................................................................................... 61

6. Alarm and troubleshooting ...................................................................................................................... 95

7. Cleaning and Disinfecting ....................................................................................................................... 112

7.1. Cleaning and disinfection of pre-use first ...................................................................................... 114

9 Remove the seal ..................................................................................................................................... 118

7.5.2. Testing Function .................................................................................................................... 118

8. User maintenance .................................................................................................................................. 123

8.1. General principle of maintenance ................................................................................................. 124

9. Technical Data ........................................................................................................................................ 132

9.1. Pneumatic Diagram ....................................................................................................................... 132

10. Appendix ............................................................................................................................................ 170

10.1. Accessories List .............................................................................................................................. 170

1.1. General Information

In terms of theory of operation, the Anesthesia Machine driven by pneumatics and

Symbol Description Symbol

CAUTION Attention, consult accompanying

Turn on power switch ON

Turn off power switch OFF

"ON" for a part of equipment

"OFF" for a part of equipment

Alternating current (AC)

Direct current (DC)

Protective earth (ground)

Authorised representative in the European community

WEEE: Waste Electronic and Electrical Waste

2: Protected against solid foreign objects of 12.5mm

1: Protection against vertically falling water drops

Rotation in two directions

Rotate to adjust(increase counter-clockwise)

Breathing bag/manual ventilation

Read the reading of the top floating-point

Outer power supply has been connected

Battery charging condition

Alarm mute icon

Interference many occur in the vicinity of equipment

Refer to product instructions

Authorized representative in the European community

This device complies with the requirements of Medical

AGSS anesthetic gas scavenging system

APL adjustable pressure limiting

BDU basic data unit