Infusion Pumps, Large-Volume

Comparative Data
Infusion Pumps, Large-Volume

Published 7/1/2018
EXECUTIVE SUMMARY
Comparison Chart
This Product Comparison covers large-volume infusion pumps (LVPs), some of which have two or more channels. Pumps in this report are calibrated in flow settings of milliliters per
hour (mL/hr) ranging from 0.1 to 3,600 mL/hr; most have a drug-/dose-calculation feature that permits programming of the flow setting directly from physician dose orders.
LVPs are used to accurately deliver liquids through intravenous (IV) or epidural routes for therapeutic and/or diagnostic purposes. They are used in hospitals, in alternative care
settings (e.g., homes, long-term care facilities, physicians' offices, outpatient infusion centers), and, occasionally, in emergency medical service vehicles.
In general, infusion pumps are used when the solution to be administered must be delivered with greater accuracy than can be provided through a manually adjusted gravity
administration set. Because they allow more accurate fluid delivery, infusion pumps have proven to be useful in applications such as continuous epidural anesthesia,
administration of IV cardiovascular drugs, chemotherapy, and autotransfusion, as well as in pediatric applications and for home IV therapy. Blood infusions can also be performed
with most pumps, although some pumps require a special administration set for this application.
LVPs can supply higher pressures than those provided by manually clamped gravity infusion sets or infusion controllers—for example, to deliver viscous fluids through micropore
bacteria filters or to deliver arterial infusions.
The following device terms and product codes as listed in ECRI Institute’s Universal Medical Device Nomenclature System™ (UMDNS™) are covered:
Infusion Pumps, Multitherapy, Large Volume [28-057]

Infusion Pumps, Multitherapy, Large Volume, MRI Safe/Conditional [28-063]
Infusion Pumps, Multitherapy, Large Volume, Multichannel [17-634]
Infusion Pumps, Multitherapy, Large Volume, Single-Channel [27-889]
These devices are also called: general-purpose infusion pumps, microinfusion pumps, multichannel pumps, volumetric infusion pumps.
Comparison Chart
Scope of this Product Comparison

This Product Comparison covers large-volume infusion pumps (LVPs), some of which have two or more channels. Pumps in this report are calibrated in flow settings of milliliters per
hour (mL/hr) ranging from 0.1 to 3,600 mL/hr; most have a drug-/dose-calculation feature that permits programming of the flow setting directly from physician dose orders.
These devices are also called: general-purpose infusion pumps, microinfusion pumps, multichannel pumps, volumetric infusion pumps.
Purpose
LVPs are used to accurately deliver liquids through intravenous (IV) or epidural routes for therapeutic and/or diagnostic purposes. They are used in hospitals, in alternative care
settings (e.g., homes, long-term care facilities, physicians' offices, outpatient infusion centers), and, occasionally, in emergency medical service vehicles.
In general, infusion pumps are used when the solution to be administered must be delivered with greater accuracy than can be provided through a manually adjusted gravity
administration set. Because they allow more accurate fluid delivery, infusion pumps have proven to be useful in applications such as continuous epidural anesthesia, administration of
IV cardiovascular drugs, chemotherapy, and autotransfusion, as well as in pediatric applications and for home IV therapy. Blood infusions can also be performed with most pumps,
although some pumps require a special administration set for this application.
LVPs can supply higher pressures than those provided by manually clamped gravity infusion sets or infusion controllers—for example, to deliver viscous fluids through micropore
bacteria filters or to deliver arterial infusions.
Principles of Operation
LVPs use one of two basic types of pumping mechanisms to move fluid from the solution container through the IV set to the patient: peristaltic or cassette.
The most common peristaltic mechanism is the linear peristaltic device, which uses fingerlike disks to occlude the IV tubing successively in a rippling, wavelike motion. The tubing is
held against a stationary backing plate and alternately compressed and released by the moving fingers, forcing the fluid to flow. Similar to the linear peristaltic device, the rotary
peristaltic pump uses a short length of silicone rubber tubing held taut around rollers mounted on a rotor. As the rotor is turned at precise speeds by a motor drive, the rollers occlude
the tubing and force the fluid from the solution container into the patient at the preselected rate. The cycling rate of either a linear or rotary peristaltic mechanism is determined by a
stepper motor, which delivers a specific volume with each pulse; varying the infusion rate changes the frequency of the pulses.
The second type of pumping mechanism uses a cassette normally fitted with either a syringelike or pistonlike device and tubing running from two sides. In syringe cassettes, a motor-
driven plunger moves into and out of a cylinder. The inward motion pumps the fluid out of the cassette toward the patient, while the outward motion draws fresh fluid from the
solution container to refill the cassette. In some cassettes, a valve directs the flow along the desired path at the appropriate times in the plunger cycle.
In piston-actuated diaphragm cassettes, a diaphragm is mounted near a moving piston that displaces a fraction of a milliliter of fluid toward the patient with each inward stroke and
allows the diaphragm to refill with each outward stroke. A valve assembly directs the flow along the desired path at the appropriate time in the plunger cycle. This pumping mechanism
delivers the infusate in discrete volume increments, normally in a pulsating flow. The flow is automatically controlled by varying the piston stroke length and rate. Some pumps use a
pair of pistons to infuse the solution through a dual-chamber cassette.
Most infusion pumps allow the user to select the dose or volume to be infused (VTBI). If this limit is reached before the fluid source is depleted, most pumps will alarm and continue
infusing fluid at a very low rate to prevent the infusion catheter from clogging. This low flow is referred to as the “keep vein open," or “KVO," rate.
Many pumps can deliver secondary (piggyback) infusions, controlling two different solutions sequentially per pumping channel. A variety of mechanisms control primary and secondary
infusions; most pumps require a special administration set with a check valve that prevents secondary infusate from flowing up to the primary bag. Pumps capable of piggyback
delivery can be programmed to revert to a primary flow setting after the secondary infusion dose is delivered. Many models require users to hang the primary bag lower than the
secondary bag; gravity forces the secondary bag to flow until it is empty, at which time the primary bag begins to flow again.
Pumps may have more than one infusion channel. Multichannel devices can simultaneously infuse from and monitor two or more IV lines and can be substituted for several single-
channel infusion pumps that might be used on one patient. One model is modular, permitting up to four pump modules to be attached to a common programming module.
Most infusion pumps sold in the USA, and some marketed globally, now have a dose error reduction system (DERS) or onboard protocol library. Also called “smart pumps," these
devices aid in prevention and warn users of programming errors that could result in under- or overdelivery, and some systems include starting dose parameters. These systems allow
infusion pumps to warn users if the rate programmed is above the set limit for that medication, calculation errors, or misprogramming that would result in significant under- or
overdelivery of a drug, electrolyte, or other fluid. DERS are an important part of a facility's defenses against medication errors and are available on large-volume (also known as
general-purpose), syringe, patient-controlled analgesic (PCA), and ambulatory pumps. To implement such a system, a facility must establish standardized concentrations and
minimum/maximum dose limits for pain medications used in each clinical location (including limits for continuous, bolus, and total dose parameters); all pumps are then programmed
with these parameters in a drug or protocol library.
To give an infusion, a nurse selects the appropriate clinical location/application (e.g., "ICU" or “orthopedic post-op") and then the correct drug entity (name, volume of the reservoir,
and concentration or total drug amount in diluent). The clinician then enters any required patient-specific parameters like starting dose parameters and weight, and the pump will
display a warning if programmed parameters would result in a rate that is outside the predetermined limits for the selected drug. For “soft limits," the nurse can either change the
programmed dose or override the warning and start the pump as programmed. For “hard limits," the nurse must change the settings so that the dose is within the acceptable limits.
Many infusion pumps with a protocol library have both soft- and hard-limit capabilities, which gives the facility the ability to set up the drug library so that any given drug entity may
have only soft limits, only hard limits, or soft limits nested within hard limits. The drug name and concentration are also displayed during infusion.
Some pumps that lack full DERS features offer a programmable or downloadable drug library that allows a clinician to program a pump by selecting a dosing protocol from a computer
via a wired or wireless connection. When a clinician chooses a protocol, the pump is populated with the drug name, concentration, starting dose, time-based dosing limit, and lockout
interval, thus eliminating the possibility of entry errors in initial programming.
Pumps have a series of alarms that warn the operator of conditions in the infusion system that could be harmful to the patient. These include air in line, upstream or downstream
occlusion, empty fluid container, set disengagement, and flow error. Alarm conditions are detected by pressure and/or ultrasonic transducers and optical sensors. A few pumps can
interface with the facility's nurse call system to send alarm conditions to the central nursing station.
Most pumps also have a memory that can retain the programmed settings and the total volume infused in case of temporary power interruption. Most pumps with memory can log
data, such as pump settings, alarm occurrences, system errors, user key presses, and the time and date of each event. In addition, a data port, such as an RS232 or Ethernet port,
allows hospitals to retain electronic or hard copies of infusion data. Some pumps have optional wireless capabilities for transferring data (such as more detailed logs or drug libraries)
to and from a centralized server over a hospital's wireless network.
Many infusion pumps are wireless, which enables wireless drug library updates, infusion pump log analysis, and pump integration. Infusion pump integration is the connecting of pump
servers with other information systems to ensure that pump programming matches provider orders. There are two ways to integrate, namely autoprogramming and
autodocumentation. Autoprogramming increases the safety of infusions by engaging the pump's drug library as well as preventing manual data entry errors. Autodocumentation
automatically populates the patient's records with accurate infusion administration information, thus reducing the documentation burden on caregivers and expediting workflow.
Reported Problems
Infusion devices are the subject of many adverse incident reports to the Food and Drug Administration (FDA) and the consequences of infusion errors can be severe. Patients can be
highly sensitive to the amount of medication or fluid they receive from infusion pumps, and some medications are life-threatening if administered in the wrong amounts or to the
wrong patient. In April 2010, FDA issued a white paper about improving infusion pump safety and announced that it would be looking into the devices in order to aid in the
development of safer and more effective infusion technologies and practices. FDA noted that many of the reported infusion pump problems were unrelated to manufacturer or
brand, or even technology; the most common problems included software defects and user interface issues (e.g., confusing or unclear instructions). Medication errors due to infusion
pump mechanism malfunctions occur less frequently, usually when a pump has been damaged or in rare instances of problems with pump administration sets.
Medication errors that occur with infusion pumps often result from (1) an operator failing to correctly program the infusion order into the pump or (2) a physician issuing an incorrect
or inappropriate order. Such errors can be reduced by establishing clear protocols for ordering infusions and programming pumps (e.g., double-checking medication orders) and by
using pumps with dose-calculation capabilities; these steps will simplify or even eliminate the somewhat error-prone process of performing manual dose calculations. However, even
when these measures are observed, administration errors can still occur (e.g., if a decimal point is omitted or if an incorrect dosing unit is programmed).
Gravity flow, or free-flow (a situation in which fluid flows into the patient without being controlled by the infusion pump) used to be a significant risk of infusion therapy, but over-
infusion due to gravity flow is rarely reported now that ECRI Institute and the Joint Commission consider infusion pumps without set-based free-flow protection to be unacceptable for
purchase or rental. However, gravity flow can still occur if the operator manually opens the set's anti-free-flow clamp or valve.
Infiltration (also called extravasation) is the extravascular accumulation of a solution being infused. This can result in tissue irritation, compartment syndrome, or tissue necrosis; in
addition, the patient is denied the necessary fluids or medications. A number of infiltration incidents have been reported to ECRI Institute implicating all types of infusion pumps.
However, infusion pumps typically play only an ancillary role in such incidents, and the belief that pumps themselves produce infiltration is inaccurate. Rather, the usual causes of
infiltration are dislodgment or improper insertion of either a catheter or, in the case of a subcutaneous injection port, a needle. Thus, to avoid problems, staff members should
monitor IV sites of patients who are receiving infusions through pumps at least hourly to ensure that catheter or needle dislodgment and subsequent infiltration do not occur.
ECRI Institute has received reports about infusion pump cleaning-related problems including difficulty with complying with manufacturer's cleaning instructions and inappropriate
cleaning methods that can result in equipment damage and affect the device's functionality. Repeated use of incompatible cleaning agents can damage equipment surfaces and
degrade plastics, resulting in equipment malfunction including improper battery or inter-unit interface connections. These connection failures can result in frequent alarms, infusion
interruptions, and potentially patient harm.
An inconsistency in the time format between the infusion pump and the EMR can lead to confusion and incorrect time entry on the infusion pump. If the time is entered incorrectly,
infusion therapy rate may be affected resulting in overinfusion or underinfusion of medication, which can lead to patient harm. ECRI Institute recommends verifying time entry format
or using pump integration to avoid the need for manual data entry on the pump to help avoid this hazard.
Infusion errors can be deadly, but simple safety practices can greatly decrease the likelihood of harm. These steps include noticing signs of physical damage to the infusion pump
components, ensuring appropriate use of the roller clamp on the IV tubing, and checking the drip chamber beneath the medication reservoir for unexpected flow. These practices are
commonplace and critical for patient safety.
Purchase Considerations
ECRI Institute Recommendations
Included in the accompanying comparison chart are ECRI Institute's recommendations for minimum performance requirements for LVPs. In general, LVPs should be able to provide a
flow of 0.1 to at least 999 mL/hr and maintain an accurate flow rate to within 5% of flow settings.
ECRI Institute believes that pumps with a DERS will significantly reduce calculation, transcription, and misprogramming errors. ECRI Institute does not recommend using an infusion
pump without a DERS for general patient care. The library should cover at least 10 care areas with at least 100 drug entities per care area. Some units may be able to be extensively
configured with each drug entity and care area. Units that default to the DERS ensure that the user is forced to opt out from the safety software if attempting to infuse without safety
limits. The system must also be able to connect wirelessly to the Internet.
ECRI Institute considers set-based free-flow protection a required feature on all newly purchased infusion pumps. Facilities that currently own pumps that do not use anti-free-flow
infusion sets should make their replacement a very high priority. ECRI Institute has rated all pumps without set-based free-flow protection Unacceptable. The Joint Commission had
included free-flow protection in its National Patient Safety Goals since July 2002. Although the patient safety goal pertaining to free-flow protection was retired for 2006, hospitals will
still be expected to comply with the retired goal under the Joint Commission's Environment of Care standard EC 6.20 (see Health Devices 2004 Dec).
LVPs should alarm and stop infusing when air-in-line volume reaches a level of 100 µL. The alarm should also not activate in response to air volumes of less than 50 µL. This
recommendation is based on the practical consideration that volumes below 50 µL would trigger nuisance alarms for outgassed microbubbles, which are common and
nonthreatening. LVPs detect upstream occlusions. In addition, pumps should have alarms and indicators for downstream occlusions, infusion complete, set loaded improperly, door
open, circuit malfunction, and low/depleted battery. LVPs should also have a log of alarms, volume infused, dose limit warnings, and key presses. The log should be able to store
information from a full week.
The pump should be designed to revert to a KVO rate between 1 and 5 mL/hr (but not greater than the programmed flow rate) once the programmed volume is delivered. Pumps
should have an automated secondary (piggyback) infusion that switches from a programmed secondary flow rate to the primary flow rate once it has delivered the secondary volume.
ECRI Institute recommends that LVPs have integral batteries that can run for at least 5 hours at a flow rate of 25 mL/hr, are commonplace, and are easily replaced. Batteries should
fully recharge in less than 8 hours and should be capable of charging independently of the main power switch. In the case of a line-power failure, pumps should automatically switch
over to battery power. All LVPs should be fluid-proof and should automatically alarm and shut down if fluid penetrates the electronic circuitry. LVPs should also be able to connect to
the hospital's wireless network and communicate to a central pump server.
As with many devices, purchasing infusion pumps is much more complicated than it used to be. Infusion system purchases involve buying a complete drug delivery platform, including
pumps, software, and communication interfaces. In addition, if a facility plans to utilize wireless networking capabilities on its infusion pumps, they must ensure that the hospital
network is equipped to provide reliable wireless communication everywhere a pump will be. Finally, to experience the safety benefits of DERS, a large commitment to drug
standardization and drug library development is required.
Buying a pump involves establishing a long-term relationship with the pump's supplier for initial implementation, product upgrades, and ongoing support. The barrier to switching
suppliers once a facility has already implemented a smart pump model is also much higher than with traditional pumps: if a facility is going to switch, it will probably have to make
changes to the drug library, which can be time-consuming. The facility will also need to consider that the differences in operation between the devices means that users will need to
be retrained, and the differences in the log-analysis and library-editor tools may mean that it is possible to lose some of the expertise administrators have developed from working
with the previous system.
Other Considerations
Before choosing a new infusion pump, healthcare facilities should first consider their needs. Determine the number of pumping channels needed, and find out whether it is
advantageous to purchase single-channel pumps, multichannel pumps, or both. Facilities should attempt to standardize on one supplier's LVP or family of pumps (that use the same
administration set and control panel) for use throughout the hospital. Standardization will greatly simplify protocol library implementation and maintenance, user training, and supplier
involvement. If standardization on a single model is impractical, the next most desirable option is to standardize on a single supplier's product line.
Apart from the basic concerns for pump safety and performance, pumps must include data logs that store all user interactions and pumps settings. A date- and time-stamped event
log (typically activated in service mode) is extremely valuable in determining the cause of a pump-associated adverse incident. Pumps with a DERS should have a separate log that
records dose limit events and clinician responses (e.g., override soft limit, reprogram pump).
Because DERSs vary greatly in their features and functionality, evaluating these systems is a critical part of the pump selection process. Some features to look for include larger drug
libraries, wireless connectivity, log-analysis software, and interfaces between a pump server and third-party information systems. Wireless connectivity can allow pushing new drug
libraries or dosing information to the pump as well as pulling event logs from the pump. Log analysis software is useful for tracking near misses, monitoring the use of the drug library,
and for refining the library to match the clinical needs of the practice. In addition, interfaces between the pump and EMRs or pharmacy dispensing systems are desirable.
Establishing drug libraries and limits requires planning and clinician compliance. Some facilities wish to include a clinical trial in their selection process; generally, smart-pump vendors
work with facilities to identify a few representative clinical locations in which to deploy trial pumps and then develop a small drug library for those locations. Such a library is typically
limited to five or six drugs per location, with the drugs being those that pose the greatest risk or that are delivered most frequently (or some combination of both). Other vendors
prefer to forgo the trial process, opting instead for clinical simulations to allow clinicians to assess the interface and functionality of their pump model. Drug library editing and log
analysis are two of the most important elements of successful smart pump-implementation, so any pump selection process should also include an assessment of the vendors'
software applications for these functions. Hospitals should also consider the vendor's ability to assist with drug library creation, training, and overall smart pump implementation.
Pump vendors often play a valuable role in the implementation of such a system because they are generally more experienced than the hospital and can assist with specific library
development questions. Therefore, vendors who are established within several hospitals, and/or offer a comprehensive support program should be considered.
Medical device integration (MDI) is of growing interest to hospitals in the United States, and interest in connecting pump servers to other information systems is growing in two
applications: (1) automatically programming infusion pumps or checking manual programming against electronic provider orders, and (2) automatically documenting infusion status
and administration in a patient's electronic medical record. Hospitals that wish to connect their infusion pump servers to other information systems should carefully document their
expectations of such an implementation, and should carefully consider whether each pump and information system supplier can support these expectations. For further information,
refer to ECRI Institute's Health Devices citations in the bibliography of this report.
Cost Containment
Because infusion pumps entail ongoing maintenance and operating costs, the initial acquisition cost does not accurately reflect the total cost of ownership. A life-cycle cost (LCC)
analysis that takes into account the cost of software licenses, maintenance, and upgrades; disposables (e.g., primary and secondary infusion sets, needleless accessories); device
maintenance; and personnel training should be prepared. Many suppliers offer various programs for rental, lease, or purchase of infusion pumps, including volume discounts.
An acquisition decision should be based on issues such as LCC, local service support, discount rates and non-price-related benefits offered by the supplier, and standardization with
existing equipment in the department or hospital (i.e., purchasing all infusion pumps from one supplier). Prices quoted from the suppliers (not list prices) will be needed to make a
useful cost comparison. Hospitals interested in purchasing infusion pumps with a DERS should also be aware of additional fees for software licensing, software maintenance, and
implementation consulting. The software licensing fee is a one-time fee paid at the time of purchase that covers the right to use the supplier's DERS software. The software
maintenance fee is an annual fee that covers software updates, patches and virus protection, and other technical support. The implementation consulting fee is a one-time fee paid
at the time of purchase, covering services such as staff and clinician training and developing a customized drug library. ECRI Institute recommends taking advantage of supplier
licensing, maintenance, and consulting plans; therefore, hospitals should consider these fees when requesting quotes for pumps with a DERS. Fees for developing and maintaining
interfaces to other information systems (if MDI is desired) should also be considered in a cost comparison.
Stage of Development
Pumping mechanism technology has remained stable; however, notable developments include smaller and lighter pumps, and infusion pump integration.
Some pumps with DERSs offer wireless connectivity between pumps and a server, allowing the transfer of event and alarm logs from the pumps to the server in near-real-time and
the transfer of new drug libraries from the server to pumps. This capability enhances the use of DERSs by allowing for regular review of alarm and event logs for library revision (an
important maintenance activity) and updates to drug libraries without the need for locating pumps and physically connecting them to a computer.
Standardizing infusion devices that have DERS capabilities can be a struggle for facilities. Replacing pumps with DERS-capable systems may not be possible for facilities that are
under contract with an original equipment manufacturer (OEM). Standardization is also difficult in areas where pumps are purchased for specific criteria and applications. A lack of
proper training on these devices, coupled with frequent staff turnover can often negate the benefits provided by the DERS-capable pumps.
Some pumps with server-based architecture may be interfaced with other hospital information systems (e.g., pharmacy information systems, electronic medication administration
records) to populate these systems with real-time or near-real-time administration information; order-checking and auto-documentation capabilities are possible. This would require a
method of accurately associating infusion pumps with patients (e.g., bar-code readers), a network connection between the pumps and the server to populate the server with updated
log information from the pumps, and customized software to pull administration information from these logs and send it to other hospital systems. Pump integration is being driven
both by safety concerns and by the desire to electronically document infusion activities, the latter of which will allow hospitals to meet meaningful use goals required by the Health
Information Technology for Economic and Clinical Health (HITECH) Act of 2009. Infusion pump integration to computer-provided order entry systems, electronic medical records
(EMRs), and even patient monitors can dramatically reduce medication administration errors. It is rapidly expanding and is available from most vendors.
BIBLIOGRAPHY
Breland BD. Continuous quality improvement using intelligent infusion pump data analysis. Am J Health Syst Pharm 2010 Sep 1;67(17):1,446-55.
Burdeu G, Crawford R, van de Vreede M, et al. Taking aim at infusion confusion. J Nurs Care Qual 2006 Apr-Jun;21(2):151-9.
Cummings K, McGowan R. “Smart" infusion pumps are selectively intelligent. Nursing 2011 Mar;41(3):58-9.
ECRI Institute. A road map for medical device interoperability: seven key steps to help your facility establish and maintain interoperability [guidance article]. Health Devices 2013
Feb;42(2):62-6.
BD—Alaris Pump Modules: ECRI Institute members continue to report inter-unit interface connector problems [ECRI Exclusive Hazard Report]. Health Devices 2017 Nov 1.
Checklist: dose error reduction systems. Health Devices 2007 Oct;36(10):332-6.
Choosing an air-in-line alarm threshold: why we recommend 100 μL. Health Devices 2016 Feb 3.
Dose error reduction systems: features and functions. Health Devices 2015 Feb 25.
Ease of use: a critical component of infusion pumps. Health Devices 2015 Feb 25.
ECRI Institute's infusion pump criteria [guidance article]. Health Devices 2008 Feb;37(2):52-8.
Epidural infusion pumps: safe selection and use. Health Devices 2017 May 31.
Evaluation background: large-volume infusion pumps. Health Devices 2017 Jan 11.
Executive brief: top 10 health technology hazards for 2017. Health Devices 2016 Nov.
General-purpose infusion pumps [inspection and preventive maintenance procedure]. BiomedicalBenchmark. Procedure no. 416-20081015-01.
Infiltration during infusion therapy: why it occurs and how to prevent it. Health Devices 2016 Feb 3.
Infusion errors can be deadly if simple safety steps are overlooked. Health Devices 2016 Nov 4.
Infusion pump dose error reduction systems [guidance article]. Health Devices 2004 Dec;33(12):427-9.
Infusion pump inspection frequencies: how often is enough? Health Devices 2016 Feb 3.
Infusion pump integration: why is it needed, and what are the challenges? [guidance article]. Health Devices 2013 Jul;42(7):210-21.
Infusion pumps. Healthc Risk Control 2011 Jul;3, Medical Technology 15:1-9.
Infusion pumps/electronic medical records—time format inconsistency may lead to over—or underdelivery of medication [ECRI Exclusive Hazard Report]. Health Devices
Alerts 2017 Nov 30.
Infusion pumps—failure to follow manufacturers' recommended cleaning instructions may cause premature device failures. [ECRI Exclusive Hazard Report]. Health Devices
Alerts 2016 Jun 16.
Infusion pumps to consider for use with hyperbaric chambers. Health Devices 2016 Feb 17.
Infusion pumps: understanding key terms and concepts. Health Devices 2016 Feb 3.
Infusion technology purchasing: it's not just about pumps. Health Devices 2015 Feb 25.
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MR-conditional pumps: the smarter choice for infusions in the MR environment. Health Devices 2015 Jul 29.
Tips and tools for a smart pump clinical assessment. Health Devices 2017 Jan 6.
What is infusion pump integration, and which models offer it? Health Devices 2018 Jan 17.
Gebhart F. Are smart pumps being used intelligently? Drug Topic Suppl [online]. 2007 Aug 20 [cited 2017 Nov 15]. Available from Internet:
http://www.drugtopics.com/hospitalhealth-system-pharmacy.
Healthcare Technology Safety Institute. Best practice recommendations for infusion pump-information network integration. 2012 [cited 2017 Nov 15]. Available from Internet:
https://www.pharmamedtechbi.com/~/media/Supporting%20Documents/The%20Gray%20Sheet/38/33/Infusion_Pump_White_Paper_Aug4.pdf
Iacovides I, Blandford A, Cox A. Infusion standardization and dose error reduction software. Br J Nurs 2014 Jul;23 Suppl 14:S16-24.
Ibarra-Perez R, Puertolas-Balint F, Lozano-Cruz E, et al. Intravenous administration errors intercepted by smart infusion technology in an adult intensive care unit. J Patient Saf
2017 Apr 1 [Epub ahead of print].
Infusing Patients Safely. Priority issues from the AAMI/FDA infusion device summit. 2010 [cited 2017 Nov 15]. Available from Internet:
http://s3.amazonaws.com/rdcmsaami/files/production/public/FileDownloads/Summits/AAMI_FDA_Summit_Report.pdf
Koutnik E. Infusion pumps are reducing medication errors Pharm Times [online]. 2004 Nov 1 [cited 2017 Nov 15]. Available from Internet: http://www.pharmacytimes.com.
O'Brien G, Edwards S, Littlefield K, et al. Securing wireless infusion pumps in healthcare delivery organization NIST SP 1800-8 Practice Guide, DRAFT [online]. 2016 July [cited
2017 Dec 5]. Available from the Internet: https://nccoe.nist.gov/publication/1800-8/.
Phelps PK. Smart infusion pumps: implementation, management, and drug libraries. 2nd ed. Bethesda: American Society of Health-System Pharmacists; 2011.
Sparnon E. Select smarter pumps that work for you. Mater Manag Health Care 2009 Jul;18(7):30-2.
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RESOURCE LIST
Comparison Chart
Request for Proposal Template

RELATED RESOURCES
Infusion Pumps, Ambulatory

Infusion-Pumps,-Enteral-Feeding
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TOPICS AND METADATA

Topics
Infusion Therapy
;
Pain Management
;
Technology Selection
Caresetting
Ambulatory Surgery Center
;
Emergency Department
;
Home Care
;
Hospice
;
Hospital Inpatient
;
Hospital Outpatient
;
Skilled-nursing Facility
;
Trauma Center
Roles
Allied Health Personnel
;
Materials Manager/Procurement Manager
;
Nurse
Information Type
Comparative Data
UMDNS
Infusion Pumps, Multitherapy, Large Volume [28-057]
Infusion Pumps, Multitherapy, Large Volume, MRI Safe/Conditional [28-063]
Infusion Pumps, Multitherapy, Large Volume, Multichannel [17-634]
Infusion Pumps, Multitherapy, Large Volume, Single-Channel [27-889]
Manufacturer Advance Medical Technology AMPall Co Ltd Arcomed AG Ascor Med Sp z o o
Co Ltd IP-7700 Volumed µVP7000 AP 31
AM-601A
WHERE MARKETED Worldwide, except USA Worldwide, except Canada and Worldwide<1> Worldwide, except USA
USA
FDA CLEARANCE No No No No
CE MARK (MDD) Yes Yes Yes Yes
CONFIGURATION
Number of channels 1 1 1 1
Max units per pole Not specified User-configurable 8 Not specified
DISPLAY
Data displayed Time, battery capacity, infusion Infusion rate, infused volume, Infusion parameters, history All alarms and indicators, all
status, mode, rate, accumulated VTBI, infusion time, remaining infusion data, all settings
volume, pressure, bed number, time, remaining battery capacity,
drug temperature, department, IV increasing pressure level, text
specification, air bubble, empty, and symbol for alarm and pre-
completion, occlusion, faulty alarm situations, medication set-
signal, misoperation. up, other
PUMP CAPABILITIES
Flow range, mL/hr 1-1,200 0.1-1,000 0.1-999 1-1,000
Increments, mL 0.1 0.1 0.01, 0.1, 1, 10, 100, 1,000 1
KVO rate, mL/hr 1 or 3 1-10 Configurable 1-5
Accuracy, % 2 5 5 5
VTBI, mL 0-9,999 0.1-9,999 1-9,999 0.1-9,999
Automatic piggybacking Not specified No Yes No

Bolus mode Yes Yes Not specified Yes
Syringe delivery Not specified No No No
MRI conditional Not specified No Full protection with No

UniQueMRIShield
Fluid resistant IPX1 Yes IP32 Yes
Front-panel lockout Not specified Yes Yes Yes
IV SET
Free-flow protection Not specified Yes Yes Yes
Air-trapping capability, Not specified 0.05-1 mL, single bubble and/or Variable Not specified
volume accumulation over time (8-64
min)
Needleless IV connection Not specified Yes Yes Yes
ALARMS & INDICATORS
Occlusion upstream Yes Yes Yes No
Occlusion downstream Yes No Yes Yes
Detection mechanism Not specified Selectable, 9 levels Fully variable No
Pressure, psi Not specified 4.5-14.5, adjustable 0.0193-19.31 5.8-11.6 (0.145 increments)
Real-time display Not specified Yes Yes No

Air in line Yes Yes Yes Yes
System malfunction Yes Yes Yes Yes
Set loaded improperly Yes Yes Yes No
Door open Yes Yes Yes Yes
Infusion complete Yes Yes Yes Yes
Low battery Yes Yes Yes Yes
Depleted battery Yes Yes Yes Yes
Clinical advisory messages Not specified Yes Yes Yes

AUDIBLE ALARM
Displaying page 1 of 3 for current model (#1-4) above.

AM-601A
Volume control Yes Yes Yes Yes
Momentary silence Not specified 1 min to 99 hr 59 min Configurable Yes

DOSE ERROR REDUCTION No DOSAGE mode available Yes No
SYSTEM (smart technology)
Defaults to DERS on startup NA No Yes NA
Library size NA 10 drugs Configurable NA
No. of care areas NA 8 Configurable NA

No. of drug entities per NA ≤256 Configurable NA
care area
Wireless connectivity Optional NA Available NA
Autodocumentation Not specified NA With bedside module Not specified
Autoprogramming Not specified Not specified With bedside module Not specified
Log-analysis software Not specified No Yes NA
DATA PORT Not specified RS232 Wireless communication between RS232 (for printing out event logs
pumps with or without docking only)
station
EVENT LOG Yes Yes Yes Yes

Printout Not specified No Yes Yes
Number of events Not specified 0 1,500 2,000
Events stored Not specified Not specified Settings, alarms, system errors Yes
POWER SOURCE
Line power, VAC (Hz) 100-240 (50/60) 115-230 (50/60) 110-230 (50/60) 200-240 (50/60)
Battery 11.1 V Ni-MH Ni-MH Ni-Cd
Life, hr @ flow (mL/hr) 4 6 @ 25 6 @ 100 3 @ 1,000; 9 @ 25
Recharge time, hr 8 6 8 24
H x W x D, cm (in) 18.8 x 19.8 x 28.8 (7.4 x 7.8 x 10 x 19 x 25 (3.9 x 7.5 x 9.8) 24.5 x 9 x 18 (9.6 x 3.5 x 7) 23 x 14 x 23 (9 x 5.5 x 9)
11.3)
WEIGHT, kg (lb) 2.2 (4.9) 3.5 (7.7) 2.4 (5.2) 3.6 (8)
PURCHASE INFORMATION
List price Not specified $520 Not specified Not specified
Warranty 1 year 2 years 2 years 2 years
Year first sold Not specified 2004 Not specified 2008

Fiscal year Not specified Not specified Not specified January to December

AM-601A
OTHER SPECIFICATIONS None specified. Open system for all kinds of IV- None specified. User-selectable drug names;
sets; numerical keypad; FND and programmable ward names;
color LCD display; purge rate of password protection. Meets
1-1,000 mL/hr. requirements of IEC 601-1 and
ISO 9001.
UMDNS CODE(S) 27889, 28057 27889, 28057 27889, 28057, 28063 27889, 28057
LAST UPDATED December 2017 January 2018 January 2018 December 2017
Supplier Footnotes
Model Footnotes
Data Footnotes <1>Africa, Asia, Australia, Central

America, Europe, Mexico, Middle
East, South America.
Manufacturer B Braun Medical Inc A B Braun B Braun Medical Inc A B Braun B Braun Medical Inc A B Braun B Braun Medical Inc A B Braun
Group Co Group Co Group Co Group Co
Infusomat compactplus Infusomat Space Infusomat Space 2nd Generation Outlook 100 ES
WHERE MARKETED Worldwide, with exceptions Worldwide Worldwide Canada, USA
FDA CLEARANCE Not specified Yes Yes Yes

CE MARK (MDD) Not specified Yes Yes No
CONFIGURATION
Max units per pole ≤18 with B Braun Station ≤16 with B Braun Space pole ≤16 with B Braun Space pole Depends on pole
compact plus
DISPLAY
Data displayed Drug/solution name, rate, dose, Drug/solution name, rate, dose, Drug/solution name, rate, dose, Drug/solution name, rate, dose,
battery life indicator, infusion within or outside soft limits, no within or outside soft limits, no VTBI, care area, location, time
running, drug concentration, limits assigned, battery life limits assigned, battery life remaining, bolusing, indicator bar
volume, dose and time since indicator, infusion pressure, indicator, infusion pressure, with current dose/rate marker and
infusion started infusion running, drug infusion running, drug associated soft and/or hard
concentration, volume, dose and concentration, volume, dose and DoseGuard/RateGuard limit
time since infusion started, care time since infusion started, care values
unit, therapy mode, wireless unit, therapy mode, wireless
status status
PUMP CAPABILITIES
Flow range, mL/hr 0.1-1,200 0.1-1,200 0.1-1,200 0.1-999.9; 0.1-99.9 (micro)
Increments, mL Not specified 0.01 (<99.99 mL/hr), 0.1 (100- 0.01 (<99.99 mL/hr), 0.1 (100- 0.1
999.9 mL/hr), 1 (1,000-1,200 999.9 mL/hr), 1 (1,000-1,200
mL/hr) mL/hr)
KVO rate, mL/hr Not specified Configurable (limits) Configurable (limits) 0.1-3
Accuracy, % 5 5 5 5
VTBI, mL Not specified 0.1-9,999.9 0.1-9,999.9 0.1-9,999.9
Automatic piggybacking Yes Yes Yes Yes

Bolus mode Yes Yes Yes Not specified
Syringe delivery Not specified No (Perfusor Space syringe No (Perfusor Space Syringe Yes
module available) module available)
MRI conditional Not specified With MRI Station With MRI Station<1> No
Fluid resistant IP34 IP22 Yes Yes

Front-panel lockout Not specified Yes Yes Yes
IV SET
Free-flow protection Not specified Yes Yes Yes
Air-trapping capability, Not specified Single bubble alarm: 0.02-0.3 Single bubble alarm: 0.02-0.3 2-3 mL
volume mL/hr; cumulatove air alarm: 0.5- mL/hr; cumulative air alarm: 0.5-
3.8 mL/hr 3.8 mL/hr
ALARMS & INDICATORS
Occlusion upstream Not specified Yes, optional drop sensor Yes, optional drop sensor Yes
Occlusion downstream Not specified Yes Yes Yes
Detection mechanism Not specified Selectable Selectable Selectable
Pressure, psi Not specified Max 15.4 (1,060 mbar) Max 15.4 (1,060 mbar) 1.5-15
Real-time display Not specified Yes Yes Trends

Air in line Not specified Yes Yes Yes
System malfunction Not specified Yes Yes Yes
Set loaded improperly Not specified Yes Yes Yes
Door open Not specified Yes Yes Yes
Infusion complete Not specified Yes Yes Yes
Low battery Not specified Yes Yes Yes
Depleted battery Not specified Pump will run on AC power Pump will run on AC power Yes, pump will run on AC power
with depleted battery
Clinical advisory messages Not specified Yes Yes Yes
AUDIBLE ALARM

Volume control Not specified Yes Yes Yes
Momentary silence Not specified No Yes Yes

DOSE ERROR REDUCTION DoseGuard Online Suite DoseGuard, powered by First DoseGuard, RateGuard
SYSTEM (smart technology) Data Bank
Defaults to DERS on startup Not specified Yes Yes Yes
Library size 3,000 ≤1,200 drugs divided in ≤30 drug ≤1,200 drugs divided in ≤30 drug 9,000 drugs, 750 solutions
categories 16 patient condition categories 16 patient condition
profiles; ≤10 concentrations for profiles; ≤10 concentrations for
long drug name long drug name
No. of care areas ≥30 15 50 15
No. of drug entities per Not specified ≤1,200 ≤1,200 600 drugs, 50 solutions
care area
Wireless connectivity With data module Yes Yes No
Autodocumentation Not specified Yes Yes No
Autoprogramming Not specified Yes Yes No
Log-analysis software Not specified Space DoseTrac provides real Space DoseTrac provides real DoseTrac with RealTime views
time views and retrospective time views and retrospective
reporting reporting
DATA PORT Ethernet, USB, Wi-Fi, HDMI, Mini Ethernet, RS232, USB, Ethernet, RS232, USB, Nurse call interface, Ethernet
DIN 9 with Data module compact master/slave, wireless LAN, PS/2 master/slave, wireless LAN, PS/2 (configuration and download)
plus with SpaceStation and with SpaceStation and
SpaceCom SpaceCom
EVENT LOG Not specified Yes Yes Yes
Printout Not specified Yes Yes Yes
Number of events Not specified 3,000 3,000 3,024
Events stored Not specified All keystrokes/inputs and infusion All keystrokes/inputs and infusion Settings, alarms, system errors,
data data all changes, drug menu, dose
limit warning
POWER SOURCE
Line power, VAC (Hz) Not specified 100-240 (50/60) 100-240 (50/60) 120-240 (50/60)
Battery Lithium ion Ni-MH, lithium ion (Wi-Fi) Ni-MH, lithium ion (Wi-Fi) Ni-MH
Life, hr @ flow (mL/hr) 6 @ 25 12 @ 100 (Ni-MH, lithium ion), 4 12 @ 100 (Ni-MH, lithium ion), 4 7 @ 25
@ 100 (lithium ion wireless) @ 100 (lithium ion wireless)
Recharge time, hr 3 6 6 100% @ 10
H x W x D, cm (in) 9.8 x 22.9 x 22 (3.9 x 9 x 8.7) 6.8 x 21.4 x 12.4 (2.7 x 8.4 x 4.9) 6.8 x 21.4 x 12.4 (2.7 x 8.4 x 4.9) 11.4 x 30.5 x 22.2 (4.5 x 12 x 8.7)
WEIGHT, kg (lb) 1.9 (4.2) 1.4 (3.1) 1.4 (3.1) 5 (11)
List price Not specified $2,550 $2,550 $3,000
Warranty Not specified 1 year 1 year 1 year
Year first sold Not specified 2004 2004 2008

Fiscal year January to December January to December January to December January to December

OTHER SPECIFICATIONS None specified. KeyGuard non-numeric keypad KeyGuard non-numeric keypad IV Safety System; color screen
eliminates zero vs. decimal eliminates zero vs. decimal with real-time display of dose/rate
programming errors; programming errors; limits; fully customizable
SpaceStation allows ≤16 Space SpaceStation allows ≤16 Space drug/solution libraries with
pumps to be housed vertically in pumps to be housed vertically in loading dose and on-demand
a single station on a single IV a single station on a single IV bolus capabilities. Meets
pole with centralized audio and pole with centralized audio and requirements of CSA and UL
visual alarms and all powered by visual alarms and all powered by 2601-1; ISO 9001 certified.
a single power cord; change care a single power cord; change care
units without stopping infusion or units without stopping infusion or
power cycling pump; battery power cycling pump; battery
maintenance mode; battery maintenance mode; battery
check; rate calculation; data lock. check; rate calculation; data lock.
Meets requirements of CSA, IEC Meets requirements of CSA, IEC
601-1, IEC 601-2-24, and UL. 601-1, IEC 601-2-24, and UL.
UMDNS CODE(S) 27889, 28057 13215, 28057 27889, 28057 27889, 28057
LAST UPDATED March 2019<1> August 2018 August 2018 November 2017
Supplier Footnotes
Model Footnotes
Data Footnotes <1>Specifications for this model <1>Not available in USA.

have been obtained from
manufacturer’s website. As a
reference to our readers, we are
including these preliminary
specifications.
Outlook 200 ES Outlook 300 ES Outlook 400 ES Vista Basic
WHERE MARKETED Canada, USA Canada, USA Canada, USA Canada, USA
FDA CLEARANCE Yes Yes Yes Yes

CE MARK (MDD) No No No Yes
CONFIGURATION
Max units per pole Depends on pole Depends on pole Depends on pole Depends on pole
DISPLAY
Data displayed Drug/solution name, rate, dose, Drug/solution name, rate, dose, Drug/solution name, rate, dose, Mode, rate, VTBI, time, KVO rate,
VTBI, care area, location, time VTBI, care area, location, time VTBI, care area, location, time total infusion time, battery left,
remaining, bolusing, indicator bar remaining, bolusing, indicator bar remaining, bolusing, indicator bar total operation time
with current dose/rate marker and with current dose/rate marker and with current dose/rate marker and
associated soft and/or hard associated soft and/or hard associated soft and/or hard
DoseGuard/RateGuard limit DoseGuard/RateGuard limit DoseGuard/RateGuard limit
values values values
PUMP CAPABILITIES
Flow range, mL/hr 0.1-999.9; 0.1-99.9 (micro) 0.1-999.9; 0.1-99.9 (micro) 0.1-999.9; 0.1-99.9 (micro) 0.1-800
Increments, mL 0.1 0.1 0.1 0.1
KVO rate, mL/hr 0.1-3 0.1-3 0.1-3 0.1-1
Accuracy, % 5 5 5 5
VTBI, mL 0.1-9,999.9 0.1-9,999.9 0.1-9,999.9 0.1-9,999.9

Bolus mode Not specified Not specified Not specified NA
Syringe delivery Yes Yes Yes No
MRI conditional No No No No
Fluid resistant Yes Yes Yes Yes

Front-panel lockout Yes Yes Yes Yes
IV SET
Free-flow protection Yes Yes Yes Yes
Air-trapping capability, 2-3 mL 2-3 mL 2-3 mL NA
volume
Needleless IV connection Yes Yes Yes Yes

ALARMS & INDICATORS
Occlusion upstream Yes Yes Yes Yes, with drop sensor
Occlusion downstream Yes Yes Yes Yes
Detection mechanism Selectable Selectable Selectable Selectable
Pressure, psi 1.5-15 1.5-15 1.5-15 8-17
Real-time display Trends Trends Trends No

Depleted battery Yes, pump will run on AC power Yes, pump will run on AC power Yes, pump will run on AC power Yes, pump will run on AC power
with depleted battery with depleted battery with depleted battery with depleted battery
Clinical advisory messages Yes Yes Yes Yes
AUDIBLE ALARM

Momentary silence Yes Yes Yes Yes

DOSE ERROR REDUCTION DoseGuard, RateGuard, DoseGuard, RateGuard, DoseGuard, RateGuard, No
SYSTEM (smart technology) DoseScan DoseScan, DoseCom DoseScan, DoseCom
Defaults to DERS on startup Yes Yes Yes NA
Library size 9,000 drugs, 750 solutions 9,000 drugs, 750 solutions 9,000 drugs, 750 solutions NA
No. of care areas 15 15 15 NA

No. of drug entities per 600 drugs, 50 solutions 600 drugs, 50 solutions 600 drugs, 50 solutions NA
care area
Wireless connectivity No Yes Yes NA
Autodocumentation No Yes Yes NA
Autoprogramming No No Yes NA
Log-analysis software DoseTrac with log analysis DoseTrac with Analytic Services DoseTrac Analytic Services with NA
with RealTime views RealTime views
DATA PORT Nurse call interface, Ethernet Nurse call interface, Ethernet Nurse call interface, Ethernet MFC plug
(configuration and download) (configuration and download), (configuration and download),
wireless COM ports wireless COM ports
EVENT LOG Yes Yes Operation, alarms, DERS No

Printout Yes Yes Yes NA
Number of events 3,024 3,024 3,024 NA
Events stored Settings, alarms, system errors, Settings, alarms, system errors, Settings, alarms, system errors, NA
all changes, drug menu, dose all changes, drug menu, dose all changes, drug menu, dose
limit warning, all scanned limit warning, all scanned limit warning, all scanned
information information information
POWER SOURCE
Line power, VAC (Hz) 120-240 (50/60) 120-240 (50/60) 120-240 (50/60) 110-120 (50/60)
Battery Ni-MH Ni-MH Ni-MH Ni-Cd
Life, hr @ flow (mL/hr) 7 @ 25 5 @ 25 5 @ 25 3.5 @ 125
Recharge time, hr 100% @ 10 100% @ 10 100% @ 10 80% @ 10-12
H x W x D, cm (in) 11.4 x 30.5 x 22.2 (4.5 x 12 x 8.7) 11.4 x 30.5 x 22.2 (4.5 x 12 x 8.7) 11.4 x 30.5 x 22.2 (4.5 x 12 x 8.7) 24 x 14 x 20 (9.4 x 5.5 x 7.8)
WEIGHT, kg (lb) 5 (11) 5 (11) 5 (11) 3.1 (6.8)
List price $3,500 $4,000 $4,500 $2,895
Warranty 1 year 1 year 1 year 1 year
Year first sold 2008 2008 2008 2003


OTHER SPECIFICATIONS IV Safety System; color screen IV Safety System; color screen IV Safety System; color screen Continuous and piggyback
with real-time display of dose/rate with real-time display of dose/rate with real-time display of dose/rate modes, program mode for
limits; fully customizable limits; fully customizable limits; fully customizable variable infusions (9 steps),
drug/solution libraries with drug/solution libraries with drug/solution libraries with ramp/taper mode for TPN, delay
loading dose and on-demand loading dose and on-demand loading dose and on-demand mode; configurable menus allow
bolus capabilities; DoseScan bar bolus capabilities; DoseCom bolus capabilities; DoseCom features to be enabled/disabled;
coding for patient matching, wireless communication; wireless communication; integral bag stand.
programming, and infusion DoseScan bar coding for patient DoseScan bar coding for patient
authorization. Meets matching, programming, and matching, programming, and
requirements of CSA and UL infusion authorization. Meets infusion authorization. Meets
2601-1; ISO 9001 certified. requirements of CSA and UL requirements of CSA and UL
2601-1; ISO 9001 certified. 2601-1; ISO 9001 certified.
UMDNS CODE(S) 27889, 28057 27889, 28057 27889, 28057 27889, 28057
LAST UPDATED November 2017 November 2017 November 2017 November 2017
Supplier Footnotes
Model Footnotes
Data Footnotes
Manufacturer Baxter Healthcare Corp Baxter Healthcare Corp BD BD
Medication Delivery Medication Delivery Alaris GP Plus Alaris Pump Module
SIGMA Spectrum Version 8 Spectrum IQ
WHERE MARKETED Canada, Puerto Rico, USA USA Asia Pacific, Canada, Europe, Worldwide
Latin America
FDA CLEARANCE Yes Yes No Yes
CE MARK (MDD) No No Yes Yes
CONFIGURATION
Number of channels 1 1 1 ≤4
Max units per pole 8 Not specified 4 Depends on IV pole
DISPLAY
Data displayed Care area, drug name, dose rate, Care area, drug name, dose rate, Infusion status, drug name, Infusion status, drug name, dose,
rate (mL/hr), time remaining, rate (mL/hr), time remaining, profile name, primary or concentration, primary or
audio level indicator, volume audio level indicator, volume secondary, infusion rate, dose secondary, infusion rate, VTBI,
remaining, indicator for primary or remaining, indicator for primary or rate, VTBI, volume infused, time patient weight (if used), volume
secondary, alarms, network secondary, alarms, network remaining, downstream occlusion infused, profile name, dataset
status, battery level status, battery level name, channel indicator, patient
ID, dynamic pressure display,
alarm information
PUMP CAPABILITIES
Flow range, mL/hr 0.5-999 0.5-999 0.1-1,200 0.1-999
Increments, mL 0.1 (0.5-99.9 mL/hr), 1 (>99.9 0.1 (0.5-99.9 mL/hr), 1 (>99.9 0.1 (0.1-99.9 mL/hr), 1 (100-999 0.1 (0.1-99.9 mL/hr), 1 (10-999
mL/hr) mL/hr) mL/hr), 10 (1,000-1,200 mL/hr) mL/hr)
KVO rate, mL/hr Defined in drug library Defined in drug library; 1 default 0.1-20 0.1-20 (0.1 mL increments)
Accuracy, % 5 5 5 @ 1-1,200 mL/hr, 10 @ 0.1-0.9 5.5 @ ≤1 mL/hr, 5 @ >1-999.9

mL/hr mL/hr
VTBI, mL 0.1-9,999 0.1-9,999 1-9,999 0.1-9.99 (0.001 increments), 10-
999.9 (0.1 increments), 1,000-
9,999 (1 increments)
Automatic piggybacking Yes Not specified Yes Yes
Bolus mode Yes Yes Yes Yes
Syringe delivery No No No Yes
Fluid resistant Yes IPX2 IPX3 IPX1

Front-panel lockout Keypad lock Keypad lock Yes Yes
IV SET
Free-flow protection Set-based NA Yes Yes
Air-trapping capability, NA NA No No
volume

ALARMS & INDICATORS
Occlusion upstream Yes Yes Yes Yes
Detection mechanism Ultrasonic, pressure transducer, Ultrasonic, pressure transducer, Downstream sensor Selectable
relative pressure relative
Pressure, psi 6 ±4, 13 ±6, 19 ±9 6 ±4, 13 ±6, 19 ±9 1-18.36 0.5-10.2
Real-time display Yes Yes Yes Yes

Set loaded improperly Yes Yes Yes Yes

AUDIBLE ALARM

Volume control Yes Yes Low, medium, high Level 1-5
Momentary silence 2 min Not specified Yes Yes

DOSE ERROR REDUCTION Includes titration error prevention Yes Guardrails Guardrails Suite MX
Defaults to DERS on startup Yes Yes Yes No default mode, clinician to

choose
Library size 5,000 5,000 3,000 protocols 10,000 drugs and fluids
No. of care areas 32 32 30 30

No. of drug entities per Not specified Not specified 100 1,500
care area
Wireless connectivity Yes Yes Via Alaris Gateway Workstation Yes
(AGW)
Autodocumentation Yes Yes Via Alaris Gateway Workstation Yes
(AGW)
Autoprogramming No Yes No Yes
Log-analysis software Via wireless Yes Yes Yes
DATA PORT RS232, IrDA IrDA RS232, IrDA RS232 (RJ45), wireless

Printout Via computer Not specified Yes Yes
Number of events ≥4,500 4,500 (minimum) 135,000 ≥10,000
Events stored Parameter settings, alarms, Time stamp, system errors, drug All All, including Guardrails alerts
power source, time stamp, IV set limit violations, others with subsequent programming
events, pump events, drug errors,
others
POWER SOURCE
Line power, VAC (Hz) 100-240 (50/60) 100-240 (50/60) 100-230 (50/60) 100-240 (50/60)
Battery Lithium ion, standard and Lithium ion Ni-MH Ni-MH

wireless
Life, hr @ flow (mL/hr) 8 @ 125 (at highest backlight 4 @ 125 (at highest backlight 5.5 @ 25 6 @ 25 (1 channel)
setting, new battery) setting, new battery)
Recharge time, hr 12 16 2.5 @ 95% 4 @ 95%
H x W x D, cm (in) 14.7 x 10.6 x 6.4 (5.8 x 4.2 x 2.5) 19.1 x 19.7 x 14 (7.5 x 7.8 x 5.5) 22.5 x 14.8 x 14.8 (8.8 x 5.8 x 22.6 x 8.4 x 14 (8.9 x 3.3 x 5.5)
5.8) pump module; 22.4 x 17.5 x 22.9
(8.8 x 6.9 x 9) PC unit
WEIGHT, kg (lb) 0.95 (2.1) 1.5 (3.2) 2.5 (5.5) 1.2 (2.6) pump module; 3.3 (7.2)
PC unit
List price $3,200 Not specified Not specified $3,000
Warranty 1 year Not specified 2 years 1 year
Year first sold 2015 2018 2006 2001

Fiscal year Not specified Not specified October to September October to September

OTHER SPECIFICATIONS Drug library/DERS prevents None specified. None specified. Includes Guardrails Suite MX
potential programming errors Software; Alaris EtCO2 Module,
before infusion begins; titration Alaris PCA Module, Alaris
error prevention system catches Syringe Module, Alaris Auto-ID
potential programming errors Module (bar-code reader) and
within the soft limits; 27 Alaris Systems Manager.
continuous dose modes (+1 for
cyclic) plus 18 amount/time dose
modes; uses standard IV sets
(Baxter); human-factors
engineered, field upgradable.
UMDNS CODE(S) 27889, 28057 13215, 27889, 28057 27889, 28057 17634, 28057
LAST UPDATED December 2017 August 2018 December 2017 December 2017
Supplier Footnotes
Model Footnotes <1>Model 8100. Formerly
marketed as Medley Medication
System.
Data Footnotes
Manufacturer BD CODAN ARGUS AG CODAN ARGUS AG Daiwha Corp Ltd
Alaris VP Plus ARGUS 717 V ARGUS 718 V Medifusion DI-2000
WHERE MARKETED Canada, Europe, South America Worldwide, except Canada and Worldwide, except Canada and Worldwide, with exceptions
USA USA
CONFIGURATION
Max units per pole 4 User-configurable User-configurable 4
DISPLAY
Data displayed Infusion status, drug name, Infusion rate, infused volume, Infusion rate, infused volume, Infusion rate, infusion volume,
profile name, primary or VTBI, infusion time, remaining VTBI, infusion time, remaining time
secondary, infusion rate, dose time, remaining battery capacity, time, remaining battery capacity,
rate, VTBI, volume infused, time increasing pressure level, text increasing pressure level, text
remaining, line pressure, and symbol for alarm and pre- and symbol for alarm and pre-
downstream occlusion alarm situations, medication set- alarm situations, medication set-
up, other up, other
PUMP CAPABILITIES
Flow range, mL/hr 0.1-1,200 0.1-1,200 0.1-1,200 0.1-99.9, 100-1,200
Increments, mL 0.1 (0.1-99.9 mL/hr), 1 (100-999 0.1 0.1 0.1 (0.1-99.9 mL/hr), 1 (100-
mL/hr), 10 (1,000-1,200 mL/hr) 1,200 mL/hr)
KVO rate, mL/hr 0.1-20 0 or 0.1-10 1 or 0.1-10 1-9 or 0.1
Accuracy, % 5 @ 1-1,200 mL/hr, 10 @ 0.1-0.9 5 5 5

mL/hr
VTBI, mL 1-9,999 0.1-999.9 0.1-999.9 0-9,999
Automatic piggybacking Yes No No No

Syringe delivery No No No No
Fluid resistant IPX3 Yes Yes Yes

IV SET
Free-flow protection Yes Yes Integral set-based Yes
Air-trapping capability, No 0.05-1 mL, single bubble and/or 0.05-1 mL, single bubble and/or Not specified
volume accumulation over time (8-64 accumulation over time (8-64
min) min)
Needleless IV connection Yes Yes Yes Not specified
ALARMS & INDICATORS
Detection mechanism In-line pressure monitoring Selectable, 10 levels Selectable, 10 levels Selectable
Pressure, psi 0.02-18.36 1.4-14.5, adjustable 1.4-14.5, adjustable 2.1-18.4 (110-950 mm Hg)


AUDIBLE ALARM

Volume control Configurable (ramping, low, Yes Yes Yes

medium, high)
Momentary silence Yes 1 min to 99 hr 59 min 1 min to 99 hr 59 min Yes
DOSE ERROR REDUCTION Guardrails ARGUSmedDB ARGUSmedDB No
Defaults to DERS on startup Yes No No NA
Library size 3,000 drug protocols 256 drugs 256 drugs NA
No. of care areas 30 8 8 NA

No. of drug entities per 100 ≤256 256 NA
care area
Wireless connectivity Via Alaris Gateway Workstation NA NA NA
(AGW)
Autodocumentation Via Alaris Gateway Workstation Not specified Not specified NA
(AGW)
Autoprogramming No Not specified Not specified NA
Log-analysis software Yes Yes Yes NA
DATA PORT RS232, IrDA RS232 RS232 RS485, USB

Printout Yes Yes Yes No
Number of events 135,000 1,000 1,000 2,000
Events stored All Settings, alarms, system errors, Settings, alarms, system errors, Yes
rate changes, configuration, rate changes, configuration,
others others
POWER SOURCE
Line power, VAC (Hz) 100-230 (50/60) 115/230 (50/60) 115/230 (50/60) 100-240 (50/60)
Battery Ni-MH Ni-MH Ni-MH Ni-MH
Life, hr @ flow (mL/hr) 5.5 @ 25 6 @ 25 6 @ 25 4 @ 100
Recharge time, hr 2.5 @ 95% 9 9 10
H x W x D, cm (in) 22.5 x 14.8 x 15.8 (8.8 x 5.8 x 16 x 19 x 13 (6.3 x 7.4 x 5.1) 16 x 19 x 13 (6.3 x 7.4 x 5.1) 12 x 13 x 20.6 (4.7 x 5.1 x 8.1)
6.2)
WEIGHT, kg (lb) 2.6 (5.7) 2 (4.4) 2 (4.4) 1.7 (3.7)
List price Not specified Not specified Not specified Not specified
Warranty 2 years 2 years 2 years 1 year
Year first sold 2013 2013 2013 Not specified

Fiscal year October to September Not specified Not specified Not specified

OTHER SPECIFICATIONS None specified. Uses standard IV sets; 4 certified Uses dedicated IV sets from None specified.
sets configurable; IV-pole, rail CODAN with patented set
mounting, or tabletop operation; integrated anti-free-flow clamp;
ARGUS 60 and 100 docking IV-pole, rail mounting, or tabletop
station compatible; LCD-display operation; ARGUS 60 and 100
for easy access to pump docking station compatible; LCD-
information, menu- and sub-menu display for easy access to pump
format, bar graph indicates line information, menu- and sub-menu
pressure; auto pressure release format, bar graph indicates line
on occlusion alarm; auto rate pressure; auto pressure release
calculation; 20 VDC supply; on occlusion alarm; auto rate
selectable options for customized calculation; 20 VDC supply;
operation; remote selectable options for customized
monitoring/computer control; operation; remote
manual/auto bolus; neonatal monitoring/computer control;
mode; flash memory for fast manual/auto bolus; neonatal
firmware updates; Windows- mode; flash memory for fast
based ARGUSservice tool; firmware updates; Windows-
continuous software upgrades. based ARGUSservice tool;
continuous software upgrades.
UMDNS CODE(S) 27889, 28057 27889, 28057 27889, 28057 27889, 28057
LAST UPDATED December 2017 January 2018<1> January 2018<1> January 2018<1>
Supplier Footnotes
Model Footnotes
Data Footnotes <1>Specifications updated using <1>Specifications updated using <1>Specifications for this model
manufacturer's website. manufacturer's website. have been obtained from
manufacturer's website. As a
reference for our readers, we are
specifications.
Manufacturer Daiwha Corp Ltd Fresenius Kabi AG Fresenius Kabi AG Fresenius Kabi AG
Medifusion DI-2200 Agilia VP Agilia VP MC WiFi Module MVP MS
WHERE MARKETED Worldwide, with exceptions Worldwide, except North America Worldwide, except North America Worldwide, except North America
CONFIGURATION
Number of channels 2 1-8 1-8 1-8
Max units per pole 4 8 8 8
DISPLAY
Data displayed Infusion rate, infusion volume, Volumetric rate, volume infused, Volumetric rate, dose rate, Rate, volume infused, VTBI,
time VTBI, pressure, drug name, volume infused, VTBI, pressure, pressure, drug name, alarm
alarm message, battery charge drug name, alarm message, message, battery charge level
level, user prompt, data log, ward battery charge level, user prompt,
name data log, ward name
PUMP CAPABILITIES
Flow range, mL/hr 0.1-1,200 0.1-1,200 0.1-1,500 0.1-1,000
Increments, mL 0.1 (0.1-99.9 mL/hr), 1 (100- 0.1 0.1 0.1 in micro mode,1 in normal
1,200 mL/hr) mode
KVO rate, mL/hr 1-9 or 0.1 3 3 3
Accuracy, % 5 5 5 5
VTBI, mL 0-9,999 1-9,999 1-9,999 1-9,999
Automatic piggybacking No No Yes Yes

Syringe delivery No In set In set In set
MRI conditional No With MRI Guard Agilia With MRI Guard Agilia No

IV SET
Air-trapping capability, Not specified NA NA NA
volume

ALARMS & INDICATORS
Occlusion upstream No Yes Yes Yes
Detection mechanism Not specified Upstream/downstream pressure Upstream/downstream pressure Upstream/downstream pressure
sensors sensors sensors
Pressure, psi Not specified 1-14.5 1-14.5 1.9-17.4


AUDIBLE ALARM

Volume control Not specified Yes Yes Yes

DOSE ERROR REDUCTION No No Yes No
Defaults to DERS on startup NA Programmable Programmable NA
Library size NA 600 600 NA
No. of care areas NA 20 20 NA

No. of drug entities per NA 200 200 NA
care area
Wireless connectivity NA No Yes No
Autodocumentation NA Yes Yes No
Autoprogramming NA No No No
Log-analysis software NA Yes Yes Yes
DATA PORT USB USB, RS232, IrDA USB, RS232, IrDA RS232

Printout No Yes Yes Yes
Number of events 2,000 1,500 1,500 768
Events stored Yes Settings alarms, system errors, Settings alarms, system errors, Settings alarms, system errors,
keys pressed keys pressed keys pressed
POWER SOURCE
Line power, VAC (Hz) 100-240 (50/60) 100-240 (50/60) 100-240 (50/60) 230 (50/60)
Battery Ni-MH Lithium-ion Lithium ion Lead
Life, hr @ flow (mL/hr) 4 @ 100 >8 @ 25 >8 @ 25 2 @ 125
H x W x D, cm (in) 12 x 21.5 x 20.6 (4.7 x 8.5 x 8.1) 14.5 x 13 x 13.5 (5.7 x 5.1 x 5.3) 14.5 x 13 x 13.5 (5.7 x 5.1 x 5.3) 10.5 x 31.5 x 13 (4.1 x 12.4 x 5.1)
WEIGHT, kg (lb) 3 (6.6) 2 (4.4) 2 (4.4) 2.4 (5.3)
Warranty 1 year 2 years 2 years 2 years
Year first sold Not specified 2015 2015 1999

Fiscal year Not specified January to December January to December January to December

OTHER SPECIFICATIONS None specified. Occlusion check system; Occlusion check system; Occlusion check system;
automatic volume/time automatic volume/time volume/time function; antibolus at
calculation; antibolus at occlusion calculation; antibolus at occlusion occlusion release; pressure-
release; pressure-increase release; pressure-increase increase warning; line-
warning; line-disconnection warning; line-disconnection disconnection warning; end-of-
warning; end-of-infusion warning; end-of-infusion infusion prealarm; bolus function;
prealarm; dose rate function, prealarm; dose rate function, macro/micro; ramp up/ramp
dose time function, drop/min dose time function, drop/min down; sequential; induction
function; bolus function; function; bolus function; loading dose; drug library.
macro/micro; ramp up/ramp macro/micro; ramp up/ramp
down; sequential; induction down; sequential; induction
loading dose; drug library; loading dose; drug library;
priming function; night mode; priming function; night mode;
extended battery life mode. extended battery life mode.
UMDNS CODE(S) 17634, 28057 17634, 28057, 28063, 27889 17634, 28057, 28063, 27889 17634, 28057, 27889
LAST UPDATED January 2018<1> January 2018 January 2018 January 2018
Supplier Footnotes
Model Footnotes
Data Footnotes <1>Specifications for this model

have been obtained from
manufacturer's website. As a
reference for our readers, we are
specifications.
Manufacturer Fresenius Kabi AG ICU Medical Inc ICU Medical Inc IRadimed Corp
Volumat MC Agilia Plum 360 Plum A+ MRidium 3860+ MRI
WHERE MARKETED North America Worldwide Worldwide Worldwide
FDA CLEARANCE Yes Yes Yes Yes

CE MARK (MDD) Yes Yes No<1> Yes
CONFIGURATION
Number of channels 1-8 1 line (2 concurrent delivery, 1 line (2 concurrent delivery, 2 with optional MRidium 3861
direct connection of secondary to direct connection of secondary to side car
cassette) cassette)
Max units per pole 8 Depends on hospital Depends on hospital 2
DISPLAY
Data displayed Volumetric rate, dose rate, Program dependent Program dependent Battery level, wireless strength,
volume infused, VTBI, pressure, channel number, time; basic
drug name, alarm message, mode: mL/hr, VTBI, VI; DERS:
battery charge level, user prompt, drug name, dose, concentration,
data log, ward name rate, infusion time remaining,
VTBI, VI, bolus; optional: SpO2%,
BPM, PI graph
PUMP CAPABILITIES
Flow range, mL/hr 0.1-1,500 0.1 to 999 0.1 to 999 0.1-1,400
Increments, mL 0.1 in micro mode,1 in normal 0.1 (0.1-99.9 mL/hr), 1 (100-999 0.1 (0.1-99.9 mL/hr), 1 (100-999 0.1 (0.1-99.9mL/hr), 1 (100-1,400
mode mL/hr) mL/hr) mL/hr)
KVO rate, mL/hr 3 1, or the last delivery rate on the 1 or continue current rate Adjustable, 0-5
associated line (whichever is
less)
Accuracy, % 5 5 (1-999 mL/hr), 10 (0.1-0.9 5 (1-1-999 mL/hr), 10 (0.1-0.9 5 (1-1,400 mL/hr), 10 (0.1-0.9
mL/hr) mL/hr) mL/hr)
VTBI, mL 1-9,999 0.1-9,999 0.1-9,999 0.1-999

Bolus mode Yes Yes No Yes
Syringe delivery In set Yes Yes Yes
MRI conditional No No No 0.2 to 3 T (≤10,000 Gauss line)
Fluid resistant Yes IPX2 IPX1 Yes

IV SET
Air-trapping capability, NA 2 mL 2 mL No
volume

ALARMS & INDICATORS
Detection mechanism Upstream/downstream pressure Selectable Selectable Integrated pressure sensors
sensors
Pressure, psi 1-14.5 1-15 1-15 1-10

Clinical advisory messages Yes No No Yes

AUDIBLE ALARM


DOSE ERROR REDUCTION Yes ICU Medical MedNet ICU Medical MedNet Yes
Defaults to DERS on startup Programmable Yes No Yes
Library size 600 2,500 (medications used in 2,700 drugs 50 entries

multiple clinical care areas and
count as a single entry)
No. of care areas 20 40 18 1 (MRI ward)

No. of drug entities per 120 400 150 50
care area
Wireless connectivity No Yes Yes Yes to remote control unit
Autodocumentation No Yes Yes No
Autoprogramming No Yes Yes No
Log-analysis software Yes Yes Yes Yes
DATA PORT USB, RS232, IrDA Yes Yes Custom RS232

Printout Yes Yes Yes Yes
Number of events 1,500 ~1 year ~1 year ≥5,000
Events stored Settings alarms, system errors, Settings, alarms, alerts, system Settings, alarms, alerts, system Memory retains each operating
keys pressed errors, hard and soft limits errors, hard and soft limits step and alarm
POWER SOURCE
Line power, VAC (Hz) 100-240 (50/60) 120 (50/60), 50 VA 120 V (50/60), 50 VA 100-240 (50/60)
Battery Lithium ion Internal sealed lead-acid Internal sealed lead-acid Rechargeable lithium polymer
rechargeable 6 V rechargeable 6 V pack, 14.8 V @ 5.8 Ah
Life, hr @ flow (mL/hr) >8 @ 125 >6 @ 125 3 @ 125, or delivers 250 mL total >12 @ 125; 4 @ 999
volume if pumping at a rate of
≥126 mL/hr
Recharge time, hr 6 ≤8 hours operating at 125 mL/hr ~6 hours with the device <9 to 95%
on one line operating at 125 mL/hr on one
line
H x W x D, cm (in) 14.5 x 13 x 13.5 (5.7 x 5.1 x 5.3) 20 x 20 x 15 (8 x 8 x 6) 20.3 x 20.3 x 15.2 (8 x 8 x 6) 15.2 x 20.3 x 22.8 (6 x 8 x 9)
WEIGHT, kg (lb) 2 (4.4) 4.5 (10) with battery 4.3 (9.5) 4.5 (9.9), 5.2 (11.4) with battery
List price Not specified $5,500 $5,095 $18,900<1>
Warranty 2 years 1 year 1 year 1 year, 1-3 years extended
available
Year first sold 2013 2015 2000 2009

OTHER SPECIFICATIONS Occlusion check system; Customizable, hospital-specific Customizable, hospital-specific Optional wireless remote for
automatic volume/time drug library; Hospira MedNet drug library; Hospira MedNet monitoring and titrating
calculation; antibolus at occlusion software provides hospital- software provides hospital- medications from the MRI control
release; pressure-increase defined best practice guidance defined best practice guidance room, DERS, sidecar; optional
warning; line-disconnection and safety rule sets supporting a and safety rule sets supporting a SpO2 monitoring available
warning; end-of-infusion hospital's drug delivery and hospital's drug delivery and utilizing Masimo technology and
prealarm; dose rate function, standardization of practices; standardization of practices; fiber optic SpO2 cable; world's
dose time function, drop/min enables delivery of concurrent enables delivery of concurrent only non-magnetic MRI infusion
function; bolus function; secondary infusion without secondary infusion without pump; Smart Pump Technology,
macro/micro; ramp up/ramp changing head height of primary changing head height of primary 0.2 to 3 T magnets, delivery via
down; sequential; induction container; enables automated container; enables automated bag, bottle or syringe, 12 battery
loading dose; drug library; backpriming to remove backpriming to remove at 125 mL/hr, optional remote
priming function; night mode; accumulated air without accumulated air without control for pump observation and
extended battery life mode. disconnecting patient line; data disconnecting patient line; data infusion titration without
transfer between MedNet server transfer between MedNet server interrupting the MRI scan.
and pump facilitated by a/b/g/n and pump facilitated by a/b/g/n
wireless functionality; the infuser wireless functionality.
has an intelligent alarm system
that handles more than one alarm
at a time; different indicators for
high, medium, and low priority
alarms; ICU Medical MedNet 6.21
forwards alarm messages to third
party alarm notification systems.
UMDNS CODE(S) 17634, 28057, 27889 17634, 28057 17634, 28057 17634, 28057, 28063
LAST UPDATED January 2018 December 2017 December 2017 December 2017
Supplier Footnotes
Model Footnotes
Data Footnotes <1>Dedicated sets only. <1>Pricing information derived

from ECRI Institute's PricePaid
database.
Manufacturer JMS North America Corp JMS North America Corp Medcaptain Medical Medcaptain Medical
OT-701 OT-711 Technology Co Ltd Technology Co Ltd
HP-60 MP-60
WHERE MARKETED Worldwide, except Europe and Worldwide, except Europe and Worldwide Worldwide
USA USA
CE MARK (MDD) No No Yes Yes
CONFIGURATION
Number of channels 1 1 1-16 1-15
Max units per pole No limit No limit 16 15
DISPLAY
Data displayed Flow status, IV set type, flow rate Flow status, IV set type, flow rate Alarm, battery symbol, dose Alarm, battery symbol, dose
setting, volume infused/volume setting, volume infused/volume concentration, drug name, flow concentration, drug name, flow
limit, alarms limit, alarms, pressure level rate, IV set brand, pressure, rate, IV set brand, pressure,
VTBI, volume infused, remaining VTBI, volume infused, remaining
infusion time, current infusion infusion time, network connection
mode, bed number, network status, relay sequence, screen
connection status, relay lock status
sequence, screen lock status
PUMP CAPABILITIES
Flow range, mL/hr 1-450 1-999 0.1-2,000 0.1-1,200
Increments, mL 1 0.1 0.01 (0.1-99.99 mL/hr), 0.1 (100- 0.01 (0.1-99.99 mL/hr), 0.1 (100-
999.9 mL/hr), 1 (1,000-2,000 999.9 mL/hr), 1 (1,000-1,200
mL/hr) mL/hr)
KVO rate, mL/hr 1 1 0.1-5 0.1-5
Accuracy, % 10, with adjusting function 5 5 5
VTBI, mL 0-9,999 0-9,999 0.1-9,999 0.1-9,999
Automatic piggybacking No Not specified No No

Bolus mode NA 0-20 mL Yes Yes
Fluid resistant IPX3 IPX3 IP23 IPX2

Front-panel lockout No No Touchscreen lockout Touchscreen lockout
IV SET
Free-flow protection Not specified Not specified Yes No
Air-trapping capability, Not specified Not specified 15 µL 25 µL
volume
Needleless IV connection Not specified Not specified Yes Yes

ALARMS & INDICATORS
Detection mechanism Magnet sensor Magnet sensor Yes Yes
Pressure, psi 8.7-20.3 8.7-20.3 2.9-18.9 4.4-18.9
Real-time display No Yes Yes Yes

Clinical advisory messages No No Yes No

AUDIBLE ALARM

HP-60 MP-60

DOSE ERROR REDUCTION No No Yes Yes
Defaults to DERS on startup NA NA Yes Yes
Library size NA NA 1,500 default, ≤5,000 1,500 default, ≤2,000
No. of care areas NA NA Configurable Configurable

No. of drug entities per NA NA Configurable Configurable
care area
Wireless connectivity NA NA Yes Yes
Autodocumentation NA NA Yes Yes
Autoprogramming NA NA Yes Yes
Log-analysis software NA NA Yes Yes
DATA PORT No No RS232, RS485, USB 2.0, USB RS485, USB

3.0, RJ45
EVENT LOG No No Yes Yes

Printout NA NA Through PC Through PC
Number of events NA NA 2,000 2,000
Events stored NA NA 2,000 2,000
POWER SOURCE
Line power, VAC (Hz) 85-264 (50/60) 85-264 (50/60) 100-240 (50/60), DC 12 V, 1 A 100-240 (50/60), DC 12 V, 1 A
Battery Ni-Cd Ni-Cd Lithium Lithium
Life, hr @ flow (mL/hr) 4 @125 4 @ 125 10 @ 25 5 @ 25
H x W x D, cm (in) 21 x 10.8 x 14.8 (8.3 x 4.3 x 5.8) 21 x 10.8 x 14.8 (8.3 x 4.3 x 5.8) 7.5 x 21.4 x 14.2 (2.9 x 8.4 x 5.6) 7.4 x 20.2 x 13.3 (2.9 x 7.9 x 5.2)
WEIGHT, kg (lb) 2.3 (5.1) 2.3 (5.1) 1.6 (3.5) 1.2 (2.6)
List price Not specified Not specified $650-800 $500-600
Warranty 1.5 years 1.5 years 18 or 24 months 18 or 24 months
Year first sold 2000 2000 2017 2013

Fiscal year April to March April to March Not specified Not specified

HP-60 MP-60
OTHER SPECIFICATIONS Continuous infusion, Continuous infusion, 11 occlusion levels; modular; 11 occlusion levels; modular;
chemotherapy, TPN, enteral chemotherapy, TPN, enteral supported by HP-80 infusion supported by MP-80 infusion
nutrition applications; standard nutrition applications; drug/dose workstation; automatic, manual, workstation; automatic, manual,
PVC IV set (OD within 3.4-4.5 calculator; JMS special infusion and rapid quantitative bolus and rapid quantitative bolus
mm and distance between ID and set (15.6 drops/mL); meets mode; stackable with syringe mode; stackable with syringe
OD within 1.25-1.35 mm) can be requirements of Class II, Type pump; automatic door; connects pump; automatic door; connects
used; meets requirements of CF. to central monitoring system; to central monitoring system;
Class II, Type CF. night mode; supports bar-code night mode; supports bar-code
scanner; automatic anti-freeflow scanner; patented design pump
clamp; float type peristaltic pump; finger; relays infusion data
patented design pump finger; between different infusion pumps
relays infusion data between using MP-80 infusion workstation.
different infusion pumps using
HP-80 infusion workstation.
UMDNS CODE(S) 27889, 28057 27889, 28057 17634, 28057 17634, 28057
LAST UPDATED November 2017 November 2017 January 2018 January 2018
Supplier Footnotes
Model Footnotes
Data Footnotes
Manufacturer Medcaptain Medical Medical Technology Products Medima Ltd Medima Ltd
Technology Co Ltd Inc P100 P200
SYS-6010 MTP
WHERE MARKETED Worldwide Worldwide Worldwide, except North America Worldwide, except North America
FDA CLEARANCE No Yes No No

CE MARK (MDD) Yes Submitted Yes Yes
CONFIGURATION
Number of channels 1, 2, 4 1 1 1
DISPLAY
Data displayed Alarm, battery symbol, dose Not specified Flow rate, bolus rate and its Flow/dose rate, bolus rate and its
concentration, drug name, flow volume, VTBI, volume, dose volume/dose, VTBI, volume/dose,
rate, IV set brand, pressure, done, ETTA, infusion pressure, dose done, ETTA, concentration,
VTBI, volume infused, remaining occlusion level, owner, battery infusion pressure, occlusion level,
infusion time, network connection status, alarms, infusion history owner, battery status, alarms,
status, screen lock status infusion history
PUMP CAPABILITIES
Flow range, mL/hr 0.1-1,200 1-499.9 0.1-1,200 0.1-1,200
Increments, mL 0.01 (0.1-99.99 mL/hr), 0.1 (100- Not specified 0.01 0.01
999.9 mL/hr), 1 (1,000-1,200
mL/hr)
KVO rate, mL/hr 0.1-5 0.5-1 0-20 0-20
Accuracy, % 5 5 5 5
VTBI, mL 0.1-9,999 1-999 or 1-9,999 0.1-20,000 0.1-20,000
Automatic piggybacking No No No No
Bolus mode Yes Not specified Yes Yes
Syringe delivery No Optional No No
MRI conditional No Not specified No No
Fluid resistant IPX2 Yes IP22 IP22

Front-panel lockout Touchscreen lockout Yes Yes Yes
IV SET
Free-flow protection No No Yes Yes
Air-trapping capability, 25 µL No 50 µL 50 µL
volume
Needleless IV connection Yes No Yes Yes

ALARMS & INDICATORS
Occlusion upstream No Yes Yes Yes
Detection mechanism Yes Configurable Yes Yes
Pressure, psi 4.4-18.9 8-12 1.45-17.4 1.45-17.4

Clinical advisory messages No Not specified Yes Yes

AUDIBLE ALARM

SYS-6010 MTP
Momentary silence Yes 1 min Yes Yes

DOSE ERROR REDUCTION No No No No
Defaults to DERS on startup NA NA NA NA
Library size 1,500 default, ≤2,000 NA NA NA
No. of care areas NA NA NA NA

No. of drug entities per NA NA NA NA
care area
Wireless connectivity Yes NA No No
Autodocumentation Yes NA No No
Autoprogramming Yes NA No No
Log-analysis software Yes NA Yes Yes
DATA PORT RS485, USB No Opto isolated and RS232C Opto isolated and RS232C
EVENT LOG Yes No Yes Yes

Printout Through PC NA No No
Number of events 2,000 NA 2,000 2,000
Events stored 2,000 NA Infusion parameters, user activity, Infusion parameters, user activity,
alarms with time and date alarms with time and date
POWER SOURCE
Line power, VAC (Hz) 100-240 (50/60), DC 12 V, 1 A 120/220 (60) 100-240 (50/60) 100-240 (50/60)
Battery Lithium Yes Ni-Mh Ni-Mh
Life, hr @ flow (mL/hr) 5 @ 25 10-12 @ 499.9 15 @ 25 15 @ 25
Recharge time, hr 10 Not specified 5 5
H x W x D, cm (in) 23 x 10 x 19 (9.1 x 3.9 x 7.5) 10.2 x 10.2 x 17.8 (4 x 4 x 7) 11.2 x 27.4 x 16.1 (4.41 x 10.79 x 11.2 x 27.4 x 16.1 (4.41 x 10.79 x
6.34) 6.34)
WEIGHT, kg (lb) 1.4 (3.1) 2 (4.5) 2.3 (5.1) 2.3 (5.1)
List price $400-450 $2,175 Not specified Not specified
Warranty 18 or 24 months 1 year 2 years 2 years
Year first sold 2013 Not specified 2017 2017

Fiscal year Not specified Not specified January to December January to December

SYS-6010 MTP
OTHER SPECIFICATIONS 11 occlusion levels; automatic, Designed for use during Automatic IV set installation and Automatic IV set installation and
manual, and rapid quantitative transport; accuracy not affected correct IV set installation control; correct IV set installation control;
bolus mode; automatic door; by motion, position, altitude, or high/medium/low priority alarms; high/medium/low priority alarms;
connects to central monitoring temperature changes; tamper programmable volume and programmable volume/dose and
system; night mode; supports alarm; upgradable software. rate/time; security; MedimaNet rate/time; security; MedimaNet
barcode scanner; patented LAN system allows monitoring of LAN system allows review of
design pump finger. pump state, firmware and pump pump state, transmission of
configuration, presents alarms, firmware and pump configuration,
history of infusion, patient data presents alarms, history of
and report printing (≤500 pumps infusion, patient data and report
per software system). printing (≤500 pumps per
software system).
UMDNS CODE(S) 17634, 27889, 28057 27889, 28057 27889, 28057 27889, 28057
LAST UPDATED January 2018 January 2018 December 2017 December 2017
Supplier Footnotes
Model Footnotes
Data Footnotes
Manufacturer Medima Ltd Mindray Mindray Mindray
P300 BeneFusion VP1 BeneFusion VP3 BeneFusion VP5
WHERE MARKETED Worldwide, except North America Worldwide, except Canada and Worldwide, except Canada and Worldwide, except Canada and
USA USA USA
CONFIGURATION
Max units per pole 8 Depends on pole Depends on pole Depends on pole
DISPLAY
Data displayed Flow/dose rate, rate limits, bolus Alarms, battery capacity, current Alarms, battery capacity, current Alarms, battery capacity, current
rate and its volume/dose, VTBI, infusion, drug name, flow rate, IV infusion, drug name, flow rate, IV infusion, drug name, flow rate, IV
volume/dose, dose done, ETTA, set brand, pressure limit, set brand, pressure limit, set brand, pressure limit,
infusion pressure, occlusion level, remaining time, total volume, remaining time, total volume, remaining time, total volume,
drug name, concentration, owner VTBI VTBI VTBI
or CCA name, battery status,
alarms, infusion history
PUMP CAPABILITIES
Flow range, mL/hr 0.1-1,200 0.1-600 0.1-1,500 0.1-2,000
Increments, mL 0.01 0.1 0.1 0.01 (0.1-99.99 mL/hr), 0.1 (100-
999.9 mL/hr), 1 (1,000-2,000
mL/hr)
KVO rate, mL/hr 0-20 0.5 0.1-5 0.1-5
Accuracy, % 5 5 5 5
VTBI, mL 0.1-20,000 0.1-9,999 0.1-9,999 0.1-9,999
Automatic piggybacking No No Yes Yes

Fluid resistant IP22 IP34 IP34 IP23

Front-panel lockout Yes Yes No Yes
IV SET
Free-flow protection Yes No Yes Yes
Air-trapping capability, 50 µL Not specified Not specified Not specified
volume

ALARMS & INDICATORS
Occlusion upstream Yes No No Yes
Detection mechanism Yes Yes Yes Yes
Pressure, psi 1.45-17.4 Low: 2.9 ±2.2 (2 kPa), medium: Low: 2.9 ±2.2 (20 kPa), medium: 1.5-18.89
10.2 ±2.2 (70 kPa), high: 17.4 10.2 ±2.2 (70 kPa), high: 17.4
±3.5 (120 kPa) ±3.5 (kPa)
Set loaded improperly Yes No No No
Clinical advisory messages Yes Not specified Not specified Not specified
AUDIBLE ALARM


DOSE ERROR REDUCTION Yes No No No
Defaults to DERS on startup No NA NA NA
Library size ≤5,000 NA NA NA
No. of care areas ≤40 NA NA NA

No. of drug entities per ≤500 NA NA NA
care area
Wireless connectivity No Yes Yes Yes
Autodocumentation No Not specified Not specified Not specified
Autoprogramming No Not specified Not specified Not specified
Log-analysis software Yes No Yes No
DATA PORT Opto isolated and RS232C RS232, nurse call RS232, nurse call RS232, nurse call

Printout No Transmit to PC and print Transmit to PC and print Transmit to PC and print
Number of events 2,000 None 1,500 2,000
Events stored Infusion parameters, user activity, None Alarm, bolus, drug information, Alarms, drug information, infusion
alarms with time and date on/off, parameter changing, data, inputs and changes
silence, start/stop infusion
POWER SOURCE
Line power, VAC (Hz) 100-240 (50/60) 100-240 (50/60) 100-240 (50/60) 100-240 (50/60)
Battery Ni-Mh Lithium Lithium Lithium
Life, hr @ flow (mL/hr) 15 @ 25 4 @ 25, optional 8 @ 25 4 @ 25, optional 8 @ 25 >9 @ 25
Recharge time, hr 5 ≤6 ≤6 ≤6
H x W x D, cm (in) 11.2 x 27.4 x 16.1 (4.41 x 10.79 x 25 x 9 x 15 (9.8 x 3.5 x 5.9) 25 x 9 x 15 (9.8 x 3.5 x 5.9) 8.7 x 17.4 x 24.5 (3.4 x 6.9 x 9.6)
6.34)
WEIGHT, kg (lb) 2.3 (5.1) <1.5 (3.2) <1.5 (3.2) <2.5 (5.5)
Warranty 2 years Not specified Not specified Not specified
Year first sold 2017 2013 2016 2013


OTHER SPECIFICATIONS Automatic IV set installation and 2.4 in LCD monochrome screen; 3 in LCD monochrome screen; 3 3 in TFT color screen; 3 basic
correct IV set installation control; general, dedicated silicone basic and 2 programmable and 3 programmable infusion
high/medium/low priority alarms; segment, and PVC IV sets; infusion modes; general, modes; general, dedicated
programmable volume/dose and dynamic pressure system. dedicated silicone segment, and silicone segment, and PVC IV
rate/time; security; MedimaNet PVC IV sets; operation guidance; sets; operation guidance;
LAN system allows review of dynamic pressure system. dynamic pressure system.
pump state, transmission of drug
libraries, firmware and pump
configuration, presents alarms,
history of infusion, patient data
and report printing (≤500 pumps
per software system).
UMDNS CODE(S) 27889, 28057 27889, 28057 27889, 28057 27889, 28057
LAST UPDATED December 2017 October 2016 October 2016 October 2016
Supplier Footnotes
Model Footnotes
Data Footnotes
Manufacturer Moog Medical Devices Group Q Core Medical Ltd Q Core Medical Ltd Samtronic Industria e
Inc Div Moog Inc Sapphire H100 SapphirePlus Comercio Ltda
AITECS 3017 ICATU
WHERE MARKETED Worldwide, except USA Chile, France, Spain, United Canada, USA Worldwide, except Canada and
Kingdom USA
FDA CLEARANCE No No Yes No
CE MARK (MDD) Yes Yes No Yes
CONFIGURATION
Max units per pole Dependent on type and stability Depends on hospital Depends on hospital 6
of pole
DISPLAY
Data displayed Infusion mode, drug name, Screen title (start up, running, Screen title (start up, running, Flow rate, time remaining, VTBI,
infusion rate, dose rate, volume paused), running icon, infusion paused), running icon, infusion dose, concentration, drug library,
infused, VTBI, time remaining to mode, battery status, infusion mode, battery status, infusion elapsed time
end of VTBI, selected occlusion parameters, pump settings parameters, pump settings,
alarm level, actual infusion wireless connection status
pressure, battery charge level,
infusion status, icons, other
infusion information
PUMP CAPABILITIES
Flow range, mL/hr 0.1-1,500 0.1-999 0.1-999 0.1-1,200 macro, 0.1-150 micro
Increments, mL 0.001 0.1 (0.1-100 mL/hr), 1 (100-999 0.1 (0.1-100 mL/hr), 1 (100-999 0.1
mL/hr) mL/hr)
KVO rate, mL/hr 0.1-20 0-20 0-20 0.1-5
Accuracy, % 5 2.5<1> 2.5<1> 5
VTBI, mL 0.1-9,999 0.1-9,999 0.1-9,999 0.1-9,999.9
Automatic piggybacking Yes Yes Yes No

Bolus mode Yes 2 modes: simple with predefined 2 modes: simple with predefined Not specified
rate or advanced with user rate or advanced with user
entered rate/time/volume entered rate/time/volume
Syringe delivery No Can pump from syringe using a Can pump from syringe using a No
vented adaptor vented adaptor
Fluid resistant IP43 IP24 IP24 Yes

IV SET
Free-flow protection INFULOCK Yes Yes No
Air-trapping capability, Pump has air-in-line detector No No NA
volume

ALARMS & INDICATORS
Occlusion upstream Yes Yes Yes With drop sensor
Detection mechanism Yes Selectable Selectable Pressure sensor (downstream)
Pressure, psi 18.4 1.5-17.4 1.5-17.4 2.9-17.4, adjustable
Real-time display Yes Yes for pressure bar No Yes

Clinical advisory messages Yes No No Yes

AUDIBLE ALARM

AITECS 3017 ICATU

DOSE ERROR REDUCTION Yes Sapphire Drug Library Editor Hospira MedNet No
Defaults to DERS on startup Yes Yes Yes NA
Library size 1,500 drug protocols ≥11,000 ≥11,000 NA
No. of care areas ≤30 40 40 NA

No. of drug entities per Configurable 1,000 3,400 NA
care area
Wireless connectivity No No Yes NA
Autodocumentation No With third party Yes Not specified
Autoprogramming Not specified With third party Yes Not specified
Log-analysis software Yes No Yes NA
DATA PORT USB; IrDA Yes Yes USB

Printout Yes Yes Yes Via computer
Number of events 2 >8,000 access through a serial >8,000 access through ICU 3,500
protocol cable from the pump to a Medical MedNet or through a
computer serial protocol cable from the
pump to a computer
Events stored Alarms, settings, configuration, Settings, infusion parameters, Settings, alarms, infusion Alarms, flow rate modification,
event time stamp, errors, rate alarms, alerts, system errors, soft parameters, alerts, system errors, start/end bolus, interrupted
data, volume data (e.g., limits hard and soft limits infusion, infusion in progress, end
delivered, VTBI), others of infusion, time/date, flow rate
POWER SOURCE
Line power, VAC (Hz) 100-240 AC adaptor 10 VDC/1.8 A AC adaptor 10 VDC/1.8 A 110-230 (50/60)
Battery Lithium ion Rechargeable lithium ion battery Rechargeable lithium ion battery Ni-MH
7.4 V, 1,960 mA/h 7.4 V, 1,960 mA/h
Life, hr @ flow (mL/hr) 10 @ 25 24 @ 125 24 @ 125 (with Wi-Fi 5 @ 125) 5 @ 25
Recharge time, hr 5 to 75% >6 >6 10
H x W x D, cm (in) 12 x 34.6 x 14 (4.7 x 13.6 x 5.5) 14.3 x 9.6 x 4.9 (5.6 x 3.8 x 1.9) 14.3 x 9.6 x 4.9 (5.6 x 3.8 x 1.9) 17 x 19.5 x 21.5 (6.7 x 7.7 x 8.5)
WEIGHT, kg (lb) 2.3 (5.1) 0.42 (0.9) 0.43 (1) 1.8 (4)
List price Not specified $3,074 (€2,500) $7,000 Not specified
Year first sold 2014 2015 2015 2016

Fiscal year October to September January to December January to December January to December

AITECS 3017 ICATU
OTHER SPECIFICATIONS Drug/dose calculator; interactive Single-platform device, Single-platform device, Purge; programmable drug library
menu; keypad lockout; preventive touchscreen user interface with 4 touchscreen user interface with 2 contains 15 drug labels;
maintenance reminder; optional modes of delivery: continuous modes of delivery: continuous adjustable bolus and KVO rate;
12 VDC power supply, mounts on with secondary and multi-step; with secondary and multi-step; titration; memory of last infusion;
Infusion Docking Station (IDS-03, TPN, intermittent, priming priming alternatives; quick clear volume feature; occlusion
IDS-04, IDS-06, IDS-08). Meets alternatives; repeat last infusion, infusion titration; resume infusion adjust; fluid balance feature; air-
requirements of IEC/EN 60601-1, preset programs, accumulated VI, after pump shut down; lock bubble size adjust; keyboard lock;
IEC/EN 60601-1-2, IEC/EN resume infusion after pump shut screen; patient lockout; accepts standard IV sets; 3
60601-1-6, IEC/EN 60601-1-8, down; lock screen; patient accumulated VI, authorization programming methods; external
IEC/EN 60601-2-24, IEC/EN lockout; authorization lock level; lock level; range parameter safety DC power supply connector, LCD
62304, IEC/EN 62366, ISO range parameter safety check; check; customizable hospital contrast/backlight adjust. Meets
14971, ISO 15223-1, EN 980, EN customizable hospital specific specific drug library; requirements of EN 60601-1, EN
1041 and TUV. drug library; immediate taper SapphirePlus with Hospira 60601-1-2, EN 60601-2-24, and
down, extensive oncology sets MedNet software provides GMP.
offering with ICU Clave hospital-defined best practice
Needleless connectors; non guidance and safety rule sets.
DEHP tubing.
UMDNS CODE(S) 27889, 28057 27889, 28057 27889, 28057 27889, 28057
LAST UPDATED April 2018 December 2017 December 2017 May 2016
Supplier Footnotes
Model Footnotes
Data Footnotes <1>Subject to external conditions <1>Subject to external conditions

such as tubing, pressure, such as tubing, pressure,
container position relative to the container position relative to the
pump, barometric pressure, pump, barometric pressure,
humidity and temperature. humidity and temperature.
Manufacturer Samtronic Industria e Samtronic Industria e Samtronic Industria e Samtronic Industria e
Comercio Ltda Comercio Ltda Comercio Ltda Comercio Ltda
ICATU S ST 1000 ST 1000 SET ST 550T2
WHERE MARKETED Worldwide, except Canada and Worldwide, except Canada and Worldwide, except Canada and Worldwide, except Canada and
USA USA USA USA
CE MARK (MDD) Yes No No No
CONFIGURATION
DISPLAY
Data displayed Flow rate, time remaining, VTBI, Flow rate, time remaining, VTBI, Flow rate, time remaining, VTBI, Flow rate, time remaining, VTBI,
dose, concentration, drug library, dose, concentration, elapsed time dose, concentration, drug library, elapsed time
elapsed time elapsed time
PUMP CAPABILITIES
Flow range, mL/hr 0.1-1,200 0.1-999.9 macro, 0.1-150 micro 0.1-999.9 0.1-999.9
KVO rate, mL/hr 0.1-5 0.1-3 0.1-3 1
Accuracy, % 5 5 5 5
VTBI, mL 0.1-9,999.9 0.1-9,999.9 0.1-9,999.9 0.1-9,999
Automatic piggybacking No No No No
Bolus mode Not specified Not specified Not specified Not specified

Front-panel lockout Yes No Yes No
IV SET
Free-flow protection Yes No No No
Air-trapping capability, NA NA NA NA
volume

ALARMS & INDICATORS
Occlusion upstream With drop sensor With drop sensor With drop sensor With drop sensor
Occlusion downstream Yes Yes Yes With drop sensor
Detection mechanism Pressure sensor (downstream) Pressure sensor (downstream) Pressure sensor (downstream) NA
Pressure, psi 2.9-17.4, adjustable 2.9-17.4, adjustable 2.9-17.4, adjustable NA
Real-time display Yes Yes Yes NA

Door open Yes Yes Yes NA

AUDIBLE ALARM


Library size NA NA NA NA

care area
Wireless connectivity NA NA NA NA
Autodocumentation Not specified Not specified Not specified NA
Autoprogramming Not specified Not specified Not specified NA
Log-analysis software NA NA NA NA
DATA PORT USB No No No
EVENT LOG Yes No No No

Printout Via computer NA NA NA
Number of events 3,500 NA NA NA
Events stored Alarms, flow rate modification, NA NA NA

start/end bolus, interrupted
infusion, infusion in progress, end
of infusion, time/date, flow rate
POWER SOURCE
Line power, VAC (Hz) 110-230 (50/60) 110-230 (50/60) 110-240 (50/60) 110-230 (50/60)
Battery Ni-MH Ni-MH Ni-MH Ni-MH
Life, hr @ flow (mL/hr) 5 @ 25 6 @ 25 6 @ 25 4 @ 25
H x W x D, cm (in) 17 x 19.5 x 21.5 (6.7 x 7.7 x 8.5) 21 x 16 x 23 (8.3 x 6.3 x 9.1) 21 x 16 x 23 (8.3 x 6.3 x 9.1) 20 x 16 x 20 (7.9 x 6.3 x 7.9)
WEIGHT, kg (lb) 1.8 (4) 2.3 (5.1) 2.3 (5.1) 1.5 (3.3)
Year first sold 2016 2000 2011 1996


OTHER SPECIFICATIONS Purge; programmable drug library Purge; adjustable bolus and KVO Purge; programmable drug library Simple and fast programming;
contains 15 drug labels; rate; titration; memory of last contains 10 drug labels; compact and light; purge; titration
adjustable bolus and KVO rate; infusion; clear volume feature; adjustable bolus and KVO rate; feature; memory of last infusion;
titration; memory of last infusion; occlusion adjust; fluid balance titration; memory of last infusion; clear volume feature; 2
clear volume feature; occlusion feature; accepts standard IV sets; clear volume feature; occlusion programming functions. Meets
adjust; fluid balance feature; air- 3 programming methods. Meets adjust; fluid balance feature; requirements of EN 60601-1, EN
bubble size adjust; keyboard lock; requirements of EN 60601-1, EN keyboard lock; adult/pediatric 60601-1-2, EN 60601-2-24, and
accepts standard IV sets; 3 60601-1-2, EN 60601-2-24, and modes; 3 programming methods. GMP.
programming methods; external GMP. Meets requirements of EN 60601-
DC power supply connector, LCD 1, EN 60601-1-2, EN 60601-2-24,
contrast/backlight adjust. Meets and GMP.
requirements of EN 60601-1, EN
60601-1-2, EN 60601-2-24, and
GMP.
UMDNS CODE(S) 27889, 28057 27889, 28057 27889, 28057 27889, 28057
LAST UPDATED May 2016 May 2016 May 2016 May 2016
Supplier Footnotes
Model Footnotes
Data Footnotes
Manufacturer Samtronic Industria e Shanghai LEIEN Medical Shenzhen Osen Technology Co Sino Medical Device
Comercio Ltda Equipment Co Ltd Ltd Technology Co Ltd
ST 550T2 Plus Enteral LINS-7 OIP-900 SN-1500H
WHERE MARKETED Worldwide, except Canada and Worldwide, except Canada and Worldwide, except Canada Worldwide
USA USA
FDA CLEARANCE No No No Not specified
CE MARK (MDD) No Yes Yes Yes
CONFIGURATION
Max units per pole 6 User-configurable Not specified Not specified
DISPLAY
Data displayed Flow rate, time remaining, VTBI, Infusion rate, infused volume, Infusion rate, infused volume, Not specified
elapsed time time SpO2, NIBP, battery level
indicator
PUMP CAPABILITIES
Flow range, mL/hr 0.1-999.9 0.1-1,200 1-1,200 0.1-1,500
KVO rate, mL/hr 1 1 or 3 1-300 0.1-5
Accuracy, % 5 5 3 5 (3 after calibration)
VTBI, mL 0.1-9,999 0.1-9,999.9 1-9,999.9 0.1-9,999
Automatic piggybacking No No Not specified Not specified

Bolus mode Not specified No Yes Not specified
Syringe delivery No No No Not specified
MRI conditional No No No Not specified
Fluid resistant Yes IPX1 Not specified IPX4

Front-panel lockout No Yes Yes Not specified
IV SET
Free-flow protection No Yes Yes Not specified
Air-trapping capability, NA No Not specified Not specified
volume
Needleless IV connection Yes Not specified Yes Not specified

ALARMS & INDICATORS
Occlusion upstream With drop sensor Yes Yes Yes
Occlusion downstream With drop sensor Yes Yes Yes
Detection mechanism NA Not specified Not specified Ultrasonic
Pressure, psi NA 8.7, 11.6, 16 Not specified 1.9, 9.7, 17.5
Real-time display NA Yes Yes Not specified

Set loaded improperly No Yes Yes Not specified
Door open NA Yes Yes Yes
Clinical advisory messages Yes Yes Yes Not specified

AUDIBLE ALARM

Volume control Yes Yes Yes Not specified
Momentary silence Yes 2 min Yes Not specified

DOSE ERROR REDUCTION No No Yes Not specified
Defaults to DERS on startup NA NA No Not specified
Library size NA NA 210 Not specified
No. of care areas NA NA Not specified Not specified

No. of drug entities per NA NA 210 Not specified
care area
Wireless connectivity NA NA NA No
Autodocumentation NA NA NA Not specified
Autoprogramming NA NA NA Not specified
Log-analysis software NA NA Yes Not specified
DATA PORT No NA Yes RS232
EVENT LOG No No Yes Yes

Printout NA NA Not specified Not specified
Number of events NA NA 1,500 1,500
Events stored NA NA Not specified Not specified
POWER SOURCE
Line power, VAC (Hz) 110-240 (50/60) 100-240 (50/60) Not specified 110-230 (50/60 Hz)
Battery Ni-MH Ni-MH Lithium ion DC12 V, 2,300 mAH
Life, hr @ flow (mL/hr) 4 @ 25 6 6 5 @ 25 mL/hr
Recharge time, hr 10 Not specified Not specified Not specified
H x W x D, cm (in) 18 x 17 x 18 (7.1 x 6.7 x 7.1) 22 x 16 x 14 (8.7 x 6.3 x 5.5) 18.8 x 19.8 x 22.8 (74 x 7.8 x 9) 14 x 30.8 x 14.4 (5.5 x 12.1 x 5.7)
WEIGHT, kg (lb) 1.4 (3.2) 2.2 (4.9) 2.5 (5.5) 2.5 (5.5)
List price Not specified Not specified $500 Not specified
Warranty 1 year Not specified Not specified Not specified
Year first sold 2016 Not specified 2011 Not specified

Fiscal year January to December February to January January to December Not specified

OTHER SPECIFICATIONS Simple and fast programming; None specified. Heating function, SpO2 and NIBP None specified.
compact and light; purge; titration vital sign parameters.
feature; memory of last infusion;
clear volume feature; 2
programming functions. Meets
requirements of EN 60601-1, EN
60601-1-2, EN 60601-2-24, and
GMP.
UMDNS CODE(S) 27889, 28057 27889, 28057 27889, 28057 13215, 27889, 28057
LAST UPDATED May 2016 January 2018 December 2017 August 2018
Supplier Footnotes
Model Footnotes
Data Footnotes
Manufacturer Sino Medical Device Sino Medical Device Sino Medical Device Sino Medical Device
Technology Co Ltd Technology Co Ltd Technology Co Ltd Technology Co Ltd
SN-1500HR SN-1600V SN-1600VR SN-1800V
WHERE MARKETED Worldwide Worldwide Worldwide Worldwide
FDA CLEARANCE Not specified Not specified Not specified Not specified
CONFIGURATION
Max units per pole Not specified Not specified Not specified Not specified
DISPLAY
Data displayed Not specified Not specified Not specified Not specified
PUMP CAPABILITIES
Flow range, mL/hr 0.1-1,500 1-1,500 1-1,500 1-1,500
KVO rate, mL/hr 0.1-5 1-5 1-5 1-5
Accuracy, % 5 (3 after calibration) 5 5 5
VTBI, mL 0.1-9,999 0.1-9,999 0.1-9,999 0.1-9,999
Automatic piggybacking Not specified Not specified Not specified Not specified
Syringe delivery Not specified Not specified Not specified Not specified
MRI conditional Not specified Not specified Not specified Not specified
Fluid resistant IPX4 IPX4 IPX4 IPX4

Front-panel lockout Not specified Not specified Not specified Not specified
IV SET
Free-flow protection Not specified Not specified Not specified Not specified
Air-trapping capability, Not specified Not specified Not specified Not specified
volume
Needleless IV connection Not specified Not specified Not specified Not specified
ALARMS & INDICATORS
Detection mechanism Ultrasonic Ultrasonic Ultrasonic Ultrasonic
Pressure, psi 1.9, 9.7, 17.5 1.9-17.4 (10 levels) 1.9-17.4 (10 levels) 1.9-17.4 (10 levels)
Real-time display Not specified Not specified Not specified Not specified
Set loaded improperly Not specified Not specified Not specified Not specified
Clinical advisory messages Not specified Not specified Not specified Not specified
AUDIBLE ALARM

SN-1500HR SN-1600V SN-1600VR SN-1800V
Volume control Not specified Not specified Not specified Not specified
Momentary silence Not specified Not specified Not specified Not specified
DOSE ERROR REDUCTION Not specified Not specified Not specified Not specified
Defaults to DERS on startup Not specified Not specified Not specified Not specified
Library size Not specified Not specified Not specified Not specified
No. of care areas Not specified Not specified Not specified Not specified
No. of drug entities per Not specified Not specified Not specified Not specified
care area
Wireless connectivity Yes No Yes No
Autodocumentation Not specified Not specified Not specified Not specified
Autoprogramming Not specified Not specified Not specified Not specified
Log-analysis software Not specified Not specified Not specified Not specified
DATA PORT RS232 RS232 RS232 RS232

Printout Not specified Not specified Not specified Not specified
Number of events 1,500 1,500 1,500 1,500
Events stored Not specified Not specified Not specified Not specified
POWER SOURCE
Line power, VAC (Hz) 110-230 (50/60 Hz) 110-240 (50/60 Hz) 110-240 (50/60 Hz) 110-240 (50/60 Hz)
Battery DC12 V, 2,300 mAH DC12 V, 2,300 mAH DC12 V, 2,300 mAH DC12 V, 2,300 mAH
Life, hr @ flow (mL/hr) 5 @ 25 mL/hr 8 @ 25 mL/hr 8 @ 25 mL/hr 8 @ 25 mL/hr
Recharge time, hr Not specified Not specified Not specified Not specified
H x W x D, cm (in) 14 x 30.8 x 14.4 (5.5 x 12.1 x 5.7) 13 x 12.9 x 21.5 (5.1 x 5.1 x 8.5) 13 x 12.9 x 21.5 (5.1 x 5.1 x 8.5) 13 x 12.9 x 21.5 (5.1 x 5.1 x 8.5)
WEIGHT, kg (lb) 2.5 (5.5) 1.8 (4) 1.8 (4) 1.8 (4)
Warranty Not specified Not specified Not specified Not specified
Year first sold Not specified Not specified Not specified Not specified
Fiscal year Not specified Not specified Not specified Not specified

SN-1500HR SN-1600V SN-1600VR SN-1800V
OTHER SPECIFICATIONS None specified. None specified. None specified. Supports speed, drip, body
weight, time and infusion plan
modes.
UMDNS CODE(S) 13215, 27889, 28057 13215, 27889, 28057 13215, 27889, 28057 13215, 27889, 28057
LAST UPDATED August 2018 August 2018 August 2018 August 2018
Supplier Footnotes
Model Footnotes
Data Footnotes
Manufacturer Sino Medical Device Sino Medical Device Sino Medical Device Smiths Medical
Technology Co Ltd Technology Co Ltd Technology Co Ltd Graseby 1200
SN-1800VR SN-2000V SN-2000VR
WHERE MARKETED Worldwide Worldwide Worldwide Worldwide, except USA
FDA CLEARANCE Not specified Not specified Not specified No

CONFIGURATION
Max units per pole Not specified Not specified Not specified Not specified
DISPLAY
Data displayed Not specified Not specified Not specified Time, volume, pressure indicator,
battery indicator, Infusion rate
unit, infusion rate value, infusion
time left
PUMP CAPABILITIES
Flow range, mL/hr 1-1,500 1-1,200 1-1,200 1-1,200
KVO rate, mL/hr 1-5 1-5 1-5 0-5
Accuracy, % 5 5 5 5
VTBI, mL 0.1-9,999 0.1-9,999 0.1-9,999 0-9,999
Automatic piggybacking Not specified Not specified Not specified Yes

Syringe delivery Not specified Not specified Not specified No
MRI conditional Not specified Not specified Not specified Not specified
Fluid resistant IPX4 IPX4 IPX4 Not specified

Front-panel lockout Not specified Not specified Not specified Not specified
IV SET
Free-flow protection Not specified Not specified Not specified Yes
Air-trapping capability, Not specified Not specified Not specified Not specified
volume
Needleless IV connection Not specified Not specified Not specified Not specified
ALARMS & INDICATORS
Detection mechanism Ultrasonic Ultrasonic Ultrasonic Not specified
Pressure, psi 1.9-17.4 (10 levels) 1.9-17.4 (10 levels) 1.9-17.4 (10 levels) Not specified
Real-time display Not specified Not specified Not specified Yes

System malfunction Yes Yes Yes Not specified
Set loaded improperly Not specified Not specified Not specified Not specified
Clinical advisory messages Not specified Not specified Not specified Not specified
AUDIBLE ALARM

SN-1800VR SN-2000V SN-2000VR
Volume control Not specified Not specified Not specified Not specified
Momentary silence Not specified Not specified Not specified Not specified
DOSE ERROR REDUCTION Not specified Not specified Not specified Not specified
Defaults to DERS on startup Not specified Not specified Not specified Not specified
Library size Not specified Not specified Not specified Not specified
No. of care areas Not specified Not specified Not specified Not specified
No. of drug entities per Not specified Not specified Not specified Not specified
care area
Wireless connectivity Yes No Yes Not specified
Autodocumentation Not specified Not specified Not specified Not specified
Autoprogramming Not specified Not specified Not specified Not specified
Log-analysis software Not specified Not specified Not specified Not specified
DATA PORT RS232 RS232 RS232 RS232
EVENT LOG Yes Yes Yes Not specified

Printout Not specified Not specified Not specified Not specified
Number of events 1,500 1,500 1,500 1,500
Events stored Not specified Not specified Not specified Not specified
POWER SOURCE
Line power, VAC (Hz) 110-240 (50/60 Hz) 110-240 (50/60 Hz) 110-240 (50/60 Hz) 110-230, 50/60 Hz
Battery DC12 V, 2,300 mAH DC12 V, 2,300 mAH DC12 V, 2,300 mAH Lithium ion
Life, hr @ flow (mL/hr) 8 @ 25 mL/hr 8 @ 25 mL/hr 8 @ 25 mL/hr 5.5 @ 25
Recharge time, hr Not specified Not specified Not specified 16
H x W x D, cm (in) 13 x 12.9 x 21.5 (5.1 x 5.1 x 8.5) 12.5 x 12.9 x 21.5 (4.9 x 5.1 x 12.5 x 12.9 x 21.5 (4.9 x 5.1 x 12 x 17 x 28.2 (4.7 x 6.7 x 11.1)
8.5) 8.5)
WEIGHT, kg (lb) 1.8 (4) 1.8 (4) 1.8 (4) 2 (4.4)
Warranty Not specified Not specified Not specified Not specified
Year first sold Not specified Not specified Not specified Not specified
Fiscal year Not specified Not specified Not specified Not specified

SN-1800VR SN-2000V SN-2000VR
OTHER SPECIFICATIONS Supports speed, drip, body Supports speed, drip, body Supports speed, drip, body None specified.
weight, time and infusion plan weight, time and infusion plan weight, time and infusion plan
modes. modes; approved for blood modes; approved for blood
infusions. infusions.
UMDNS CODE(S) 13215, 27889, 28057 13215, 27889, 28057 13215, 27889, 28057 27889, 28057
LAST UPDATED August 2018 August 2018 August 2018 July 2018
Supplier Footnotes
Model Footnotes
Data Footnotes
Manufacturer Suzhou Uniontech Import & Suzhou Uniontech Import & Terumo Corp (Japan) Terumo Corp (Japan)
Export Co Ltd Export Co Ltd Terufusion TE-171 Terufusion TE-172
M-IP1100 M-IP1200
WHERE MARKETED Worldwide, except USA Worldwide, except USA Asia, Europe, Japan, South Asia, Europe, Japan, South
America America
CONFIGURATION
Max units per pole Not specified Not specified 1 1
DISPLAY
Data displayed Infusion rate, infused volume, AC power connection, power, Flow rate, VTBI, other Flow rate, VTBI, other
VTBI, air in line, occlusion, over, volume, door open, tube,
AC/battery symbol, low battery, occlusion level, air in line,
error, door open, tube, occlusion occlusion level, low battery, over,
level error, infusion time, infusion rate,
VTBI, volume infused
PUMP CAPABILITIES
Flow range, mL/hr 0-3,600 0-3,600 0.1-1,200 0.1-1,200
Increments, mL 1 (1-600 mL/hr) 0.1 (0.1-99.9 mL/hr),1 (1-1,200 0.1 (0.1-99.9 mL/hr), 1 (100- 0.1 (0.1-99.9 mL/hr), 1 (100-
mL/hr) 1,200 mL/hr) 1,200 mL/hr)
KVO rate, mL/hr 6 1-8 1, <1 same as flow rate 1, <1 same as flow rate
Accuracy, % 2 2 3 3
VTBI, mL 1-9,999 1-9,999 0-9,999 0-9,999
Automatic piggybacking Yes Yes No No

Bolus mode Yes Yes NA NA
Syringe delivery Not specified Not specified No No
MRI conditional Not specified Not specified No No
Fluid resistant IPX3 IPX3 Yes IPX2

Front-panel lockout Not specified Not specified No No
IV SET
Free-flow protection Yes Yes No No
Air-trapping capability, Not specified Not specified ~0.04 mL ~0.04 mL
volume

ALARMS & INDICATORS
Detection mechanism Ultrasound Ultrasound Benchmarking Benchmarking
Pressure, psi Not specified Not specified 1.9-19.3 1.9-19.3
Real-time display Not specified Yes No No

Set loaded improperly Not specified Not specified Yes Yes
Clinical advisory messages Not specified Not specified Yes Yes

AUDIBLE ALARM

M-IP1100 M-IP1200


care area
Autodocumentation NA NA NA NA
Autoprogramming NA NA NA NA
DATA PORT RS485, USB, RJ45 RS485, USB, RJ45 No RS232C, RS485

Printout No Through PC No No
Number of events No 2,000 500 500
Events stored Not specified Not specified Flow rate, VTBI at time of Flow rate, VTBI at time of
start/stop, alarm occurrence start/stop, alarm occurrence
POWER SOURCE
Line power, VAC (Hz) 100-240 (50/60); 7.4 V, 1,600 100-240 (50/60); 7.4 V, 2,400 100-240 (50) 100-240 (50)
mAh mAh
Battery Lithium Lithium Ni-Cd Ni-Cd
Life, hr @ flow (mL/hr) >4 @ 25 >4 @ 25 3 @ 25 3 @ 25
Recharge time, hr 10 with power on; 3 with power 10 with power on; 3 with power 15 15
off off
H x W x D, cm (in) 13 x 13 x 8 (5.1 x 5.1 x 3.1) 13.5 x 13.5 x 9 (5.3 x 5.3 x 3.5) 21.5 x 10 x 20.8 (8.5 x 3.9 x 8.2) 21.5 x 10 x 20.8 (8.5 x 3.9 x 8.2)
WEIGHT, kg (lb) 1.3 (2.9) 1.4 (3.1) 3.6 (8) 3.7 (8.2)
List price $240-300 $260-350 $1,200 $1,200
Year first sold 2014 2014 1997 1997

Fiscal year Not specified Not specified April to March April to March

M-IP1100 M-IP1200
OTHER SPECIFICATIONS Stop error power off; air-in-line Stop error power off; 4 levels of Memory function; volume- Memory function; volume-
alarm adjustable; 3 adjustable air-in-line alarm adjustable; 3 delivered clear function. delivered clear function.
occlusion pressure settings; anti- adjustable occlusion pressure
reverse rotation detection; screen setting; anti-reverse rotation
display and output to the detection; 2,000 history records;
computer; rate mode, drip mode. screen display and output to the
computer; rate mode, drip mode,
time mode, micro mode;
adjustable buzzer volume; large,
HD LCD display; heating function;
double CPU.
UMDNS CODE(S) 27889, 28057 27889, 28057 27889, 28057 27889, 28057
LAST UPDATED February 2018 February 2018 January 2018<1> January 2018<1>
Supplier Footnotes
Model Footnotes
Data Footnotes <1>Specifications updated using <1>Specifications updated using

manufacturer's website. manufacturer's website.
Manufacturer Terumo Corp (Japan) Terumo Corp (Japan) Terumo Corp (Japan) Terumo Corp (Japan)
Terufusion TE-LF600 Terufusion TE-LF602 Terufusion TE-LM700 Terufusion TE-LM702
WHERE MARKETED Asia, Europe, Japan, Middle Asia, Europe, Japan, Middle Asia, Europe, Japan, Middle Asia, Europe, Japan, Middle
East, South America East, South America East, South America East, South America
CONFIGURATION
Max units per pole Not specified Not specified 9 9
DISPLAY
Data displayed Flow rate, VTBI, others Flow rate, VTBI, others Flow rate, VTBI, others Flow rate, VTBI, patient
information, others
PUMP CAPABILITIES
Flow range, mL/hr 0.1-999 0.1-999 0.1-1,200 0.1-1,200
Increments, mL 0.01 (0.01-10 mL/hr), 0.1 (10-100 0.01 (0.01-10 mL/hr), 0.1 (10-100 0.1 (0.1-100 mL/hr), 1 (100-1,200 0.1 (0.1-100 mL/hr), 1 (100-1,200
mL/hr), 1 (100-999 mL/hr) mL/hr), 1 (100-999 mL/hr) mL/hr) mL/hr)
KVO rate, mL/hr 3 (20 drops/mL), 1-3 (60 3 (20 drops/mL), 1-3 (60 0.1-3, <1 same as flow rate 0.1-3, <1 same as flow rate
drops/mL) drops/mL)
Accuracy, % ±10 ±10 3 3
VTBI, mL Not specified Not specified 0.1-9,999 0.1-9,999
Automatic piggybacking Not specified Not specified No No

Bolus mode Not specified Not specified Yes Yes
Fluid resistant IP22 IP22 IP22 IP22

IV SET
Air-trapping capability, Not specified Not specified ~0.05 mL ~0.05 mL
volume

ALARMS & INDICATORS
Detection mechanism Not specified Not specified Benchmarking Benchmarking
Pressure, psi 4.4-17.4 4.4-17.4 4.35-17.4 4.35-17.4
Real-time display Not specified Not specified Yes Yes

Set loaded improperly Not specified Not specified Yes Yes
Clinical advisory messages Not specified Not specified Yes Yes

AUDIBLE ALARM

Volume control Not specified Not specified Yes Yes
Momentary silence Not specified Not specified Yes Yes


care area
Autodocumentation NA NA NA NA
Autoprogramming NA NA NA NA
DATA PORT Not specified RS232C Not specified RS232C
EVENT LOG Not specified Not specified Yes Yes

Printout Not specified Not specified No No
Number of events Not specified Not specified 10,000 10,000
Events stored Not specified Not specified Flow rate, VTBI at time of Flow rate, VTBI at time of
start/stop, alarm occurrence, start/stop, alarm occurrence,
other other
POWER SOURCE
Line power, VAC (Hz) 100-240 100-240 100-120, 100-240 (50/60) 100-120, 100-240 (50/60)
Battery Lithium-ion Lithium-ion Lithium-ion Lithium-ion
Life, hr @ flow (mL/hr) 5 @ 25 5 @ 25 5 @ 25 5 @ 25
Recharge time, hr ≥8 ≥8 9 9
H x W x D, cm (in) 12 x 25.3 x 10.2 (4.7 x 10 x 4) 12 x 25.3 x 12.1 (4.7 x 10 x 4.8) 12 x 25.3 x 10.2 (4.7 x 10 x 4) 12 x 25.3 x 10.2 (4.7 x 10 x 4)
WEIGHT, kg (lb) 2 (4.4) 2 (4.4) 2 (4.4) 2 (4.4)
List price Not specified Not specified $1,600 $1,600
Warranty Not specified Not specified 1 year 1 year
Year first sold Not specified Not specified 2012 2012

Fiscal year April to March April to March April to March April to March

OTHER SPECIFICATIONS None specified. None specified. 4.3" full-color LCD display; flow 4.3" full-color LCD display; flow
rate/VTBI volume limit alarm; dial rate/VTBI volume limit alarm; dial
setting; setting step 100 times; setting; setting step 100 times;
shortcut call; power off alert; message function; shortcut call;
optional one-touch pole clamp; power off alert; optional one-
optional rack system; Class I touch pole clamp; optional rack
equipment and internally powered system; Class I equipment and
equipment, type CF. internally powered equipment,
type CF.
UMDNS CODE(S) 27889, 28057 27889, 28057 27889, 28057 27889, 28057
LAST UPDATED March 2019<1> March 2019<1> January 2018<1> January 2018<1>
Supplier Footnotes
Model Footnotes
Data Footnotes <1>Specifications for this model <1>Specifications for this model <1>Specifications updated using <1>Specifications updated using
have been obtained from have been obtained from manufacturer's website. manufacturer's website.
manufacturer’s website. As a manufacturer’s website. As a
reference to our readers, we are reference to our readers, we are
including these preliminary including these preliminary
specifications. specifications.
Manufacturer Terumo Corp (Japan) Zyno Medical Zyno Medical
Terufusion TE-LM800 Z-800F Z-800WF
WHERE MARKETED Asia, Europe, Japan, Middle USA USA

East, South America
FDA CLEARANCE No Yes Yes
CE MARK (MDD) Yes No No
CONFIGURATION
Number of channels 1 1 1
Max units per pole 9 6 6
DISPLAY
Data displayed Flow rate, patient information, Drug, rate, time, VTBI, volume Drug, rate, time, VTBI, volume
VTBI, others infused, battery strength infused, battery strength, wireless
signal strength, access point
connected
PUMP CAPABILITIES
Flow range, mL/hr 0.1-1,200 1-1,200 1-1,200
Increments, mL 0.1 (0.1-100 mL/hr), 1 (100-1,200 1 1
mL/hr)
KVO rate, mL/hr 0.1-3, <1 same as flow rate 1-5 1-5
Accuracy, % 3 5 5
VTBI, mL 0.1-9,999 1-9,999 1-9,999
Automatic piggybacking Yes Yes Yes

Bolus mode Yes No No
Syringe delivery No No No
MRI conditional No No No
Fluid resistant IP22 Yes Yes

Front-panel lockout Yes Yes Yes
IV SET
Free-flow protection Yes Yes Yes
Air-trapping capability, ~0.05 mL 10-140 µL 10-140 µL
volume
Needleless IV connection Yes Yes Yes

ALARMS & INDICATORS
Occlusion upstream Yes With drop sensor With drop sensor
Occlusion downstream Yes Yes Yes
Detection mechanism Benchmarking Built-in, adjustable air detector, Built-in, adjustable air detector,
pressure gauge pressure gauge
Pressure, psi 4.35-17.4 4-30, adjustable 4-30, adjustable
Real-time display Yes Yes Yes

Air in line Yes Yes Yes
System malfunction Yes Yes Yes
Set loaded improperly Yes Yes Yes
Door open Yes Yes Yes
Infusion complete Yes Yes Yes
Low battery Yes Yes, battery strength icon on Yes, battery strength icon on
display display
Depleted battery Yes Yes Yes
Clinical advisory messages Yes Yes Yes

AUDIBLE ALARM

Volume control Yes Yes Yes
Momentary silence Yes Yes Yes

DOSE ERROR REDUCTION Yes No ZynoFlo Integrated Infusion
SYSTEM (smart technology) System utilizes patient-specific
orders, pre-set drug infusion
parameters, and protocols
Defaults to DERS on startup Yes NA No
Library size 3,000 drugs NA Configurable when using ZynoFlo
No. of care areas 30 NA Configurable when using ZynoFlo

No. of drug entities per 100 NA Configurable when using ZynoFlo
care area
Wireless connectivity Yes NA Yes
Autodocumentation Not specified NA Yes
Autoprogramming Not specified With onboard protocol Yes

customization
Log-analysis software Yes NA Yes
DATA PORT Wi-Fi, IrDA RS232 RS232
EVENT LOG Yes Yes Yes

Printout No Laptop access With Gateway
Number of events 10,000 500 Unlimited
Events stored Flow rate, VTBI at time of Error codes, alarms, user keypad Error codes, alarms, user keypad
start/stop, alarm occurrence, actions, VTBI, VINF, flow rate, actions, VTBI, VINF, flow rate,
other infusion mode infusion mode
POWER SOURCE
Line power, VAC (Hz) 100-120, 100-240 (50/60) 100/240 (50/60) 100/240 (50/60)
Battery Lithium-ion 12 V 12 V
Life, hr @ flow (mL/hr) 5 @ 25 8 @ 125 8 @ 125
Recharge time, hr 8 5 5
H x W x D, cm (in) 12 x 25.3 x 10.2 (4.7 x 10 x 4) 21.8 x 14.4 x 13.4 (8.6 x 5.7 x 21.8 x 14.4 x 13.4 (8.6 x 5.7 x
5.3) 5.3)
WEIGHT, kg (lb) 2 (4.4) 3.2 (7) 3.2 (7)
List price $1,800 $2,475 $2,899
Warranty 1 year 1 year 1 year
Year first sold 2012 2007 2012

Fiscal year April to March January to December January to December

OTHER SPECIFICATIONS 4.3" full-color LCD display; flow Upgradable software; 45 degree Wireless pump; upgradable
rate/VTBI limit alert; link tilt mount; alarm light extension; software; 45° tilt mount; alarm
interruption alarm; dial setting; protocol feature; configurable UI; light extension; protocol feature;
shortcut call; power off alert; dose durable aluminum casing. configurable UI; durable
mode select; intermittent dose; aluminum casing; Z-800WF
multi-step dose; delayed start wireless gateway supports
dose; optional one-touch pole 802.11 b/g to enable information
clamp; optional rack system; transfer between Z-800WF
Class I equipment and internally pumps, IVSafe applications,
powered equipment, type CF. EMRs, and medication
dispensing and billing systems.
UMDNS CODE(S) 27889, 28057 27889, 28057 27889, 28057

LAST UPDATED January 2018<1> December 2017 December 2017
Supplier Footnotes
Model Footnotes
Data Footnotes <1>Specifications updated using

manufacturer's website.

Infusion Pumps, Large-Volume - 040719081048

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Comparative Data

Infusion Pumps, Multitherapy, Large Volume [28-057]

Scope of this Product Comparison

Request for Proposal Template

Infusion Pumps, Ambulatory

TOPICS AND METADATA

Max units per pole Not specified User-configurable 8 Not specified

KVO rate, mL/hr 1 or 3 1-10 Configurable 1-5

VTBI, mL 0-9,999 0.1-9,999 1-9,999 0.1-9,999

Automatic piggybacking Not specified No Yes No

Syringe delivery Not specified No No No

MRI conditional Not specified No Full protection with No

Real-time display Not specified Yes Yes No

Depleted battery Yes Yes Yes Yes

Clinical advisory messages Not specified Yes Yes Yes

Displaying page 1 of 3 for current model (#1-4) above.

Momentary silence Not specified 1 min to 99 hr 59 min Configurable Yes

Defaults to DERS on startup NA No Yes NA

Library size NA 10 drugs Configurable NA

No. of care areas NA 8 Configurable NA

Autodocumentation Not specified NA With bedside module Not specified

Log-analysis software Not specified No Yes NA

EVENT LOG Yes Yes Yes Yes

Battery 11.1 V Ni-MH Ni-MH Ni-Cd

Life, hr @ flow (mL/hr) 4 6 @ 25 6 @ 100 3 @ 1,000; 9 @ 25

Year first sold Not specified 2004 Not specified 2008

Displaying page 2 of 3 for current model (#1-4) above.

Data Footnotes <1>Africa, Asia, Australia, Central

FDA CLEARANCE Not specified Yes Yes Yes

VTBI, mL Not specified 0.1-9,999.9 0.1-9,999.9 0.1-9,999.9

Automatic piggybacking Yes Yes Yes Yes

Fluid resistant IP34 IP22 Yes Yes

Real-time display Not specified Yes Yes Trends

Displaying page 1 of 3 for current model (#5-8) above.

Momentary silence Not specified No Yes Yes

Defaults to DERS on startup Not specified Yes Yes Yes

Autodocumentation Not specified Yes Yes No

Autoprogramming Not specified Yes Yes No

Recharge time, hr 3 6 6 100% @ 10

WEIGHT, kg (lb) 1.9 (4.2) 1.4 (3.1) 1.4 (3.1) 5 (11)

Year first sold Not specified 2004 2004 2008

Displaying page 2 of 3 for current model (#5-8) above.

Data Footnotes <1>Specifications for this model <1>Not available in USA.

FDA CLEARANCE Yes Yes Yes Yes

KVO rate, mL/hr 0.1-3 0.1-3 0.1-3 0.1-1

VTBI, mL 0.1-9,999.9 0.1-9,999.9 0.1-9,999.9 0.1-9,999.9

Automatic piggybacking Yes Yes Yes Yes

Syringe delivery Yes Yes Yes No

Fluid resistant Yes Yes Yes Yes

Needleless IV connection Yes Yes Yes Yes

Pressure, psi 1.5-15 1.5-15 1.5-15 8-17

Real-time display Trends Trends Trends No

Displaying page 1 of 3 for current model (#9-12) above.

Momentary silence Yes Yes Yes Yes

Defaults to DERS on startup Yes Yes Yes NA

No. of care areas 15 15 15 NA

Autodocumentation No Yes Yes NA

EVENT LOG Yes Yes Operation, alarms, DERS No

Battery Ni-MH Ni-MH Ni-MH Ni-Cd

Life, hr @ flow (mL/hr) 7 @ 25 5 @ 25 5 @ 25 3.5 @ 125

Recharge time, hr 100% @ 10 100% @ 10 100% @ 10 80% @ 10-12

WEIGHT, kg (lb) 5 (11) 5 (11) 5 (11) 3.1 (6.8)