Critikon Dinamap Pro100-400 Service manual
PRO Series 100 - 400 V2
Service Manual
(Models 110 - 410)
DINAMAP® PRO Series 100-400V2
Monitor Service Manual
NOTE
The Model Numbers 100 through 400 are generic in nature and reflect the ran ge of product codes
available. Your product may be labeled with a specific product code such as DINAMAP
®
PRO Model 410.
“V2” refers to the second version of the product’s de sig n
2018553-001 Revision B
.
DINAMAP® PRO Series 100-400V2 Monitor Service Manual Revision B
2018553-001
DINAMAP® Series PRO 100-400V2 Monitor
Service Manual
This manual is for DINAMAP PRO Series Monitor models 100, 200, 300,
and 400, with or without printers.
• PRO 100: BP, Pulse
• PRO 200: BP, Pulse, and Temp
• PRO 300: BP, Pulse, and SpO
• PRO 400: BP, Pulse, Temp, and SpO
The model of the Monitor determines which parameters are in your mo nitor.
Please refer to applicable sections.
Reissues and Updates
Changes occurring between issues are addressed through Change
Information Sheets, Addendums, and replacement pages. If a Change
Information Sheet does not accompany this manual, it is correct as printed.
Errors and Omissions
If errors or omissions are found in this manual, please notify:
GE Medical Systems Information Technologies, Inc.
8200 West Tower Avenue
Milwaukee, WI 53223 USA
Tel: +414.355.5000
800.558.5120 (US only)
Fax:+414.355.3790
2
2
Part No. 2018553-001 B
The content of this document including all figures and dr awings is proprietary
information of GE Medical Systems Information Technologies, provided
solely for purposes of operation, maintenance or repair, and dissemination
for other purposes or copying thereof is prohibited without prior written
consent by GE Medical Systems Information Technologies.
Illustrations may show design models; production units may incorporate
changes.
Hierarchy of Warnings and Cautions
A general warning is a statement that alerts the user to the possibility of
injury, death, or other serious adverse reactions associated with the misuse
of the device. A warning relates to steps in a procedure.
A general caution is a statement that alerts the user to the possibility of a
problem with the device associated with its use or misuse. Such problems
include device malfunction, device failure, damage to the device or damage
to other property. A caution relates to steps in a procedure.
© Copyright 2004, GE Medical Systems Information Technologies. All rights
reserved.
Revision B DINAMAP® PRO Series 100-400V2 Monitor Service Manual
2018553-001
World Headquarters
GE Medical Systems Information Technologies, Inc.
8200 West Tower Avenue
Milwaukee, WI 53223 USA
Tel: +414.355.5000
800.558.5120 (US only)
Fax:+414.355.3790
European Representative
GE Medical Systems
Information Technologies GmbH
Munzinger Straße 3-5
D-79111 Freiburg
Germany
Tel: + 49 761 45 43 - 0
Fax: + 49 761 45 43 - 233
Asia Headquarters
GE Medical Systems
Information Technologies Asia; GE (China) Co., Ltd.
24th Floor, Shanghai MAXDO Center,
8 Xing Yi Road, Hong Qiao Development Zone
Shanghai 200336, P.R. China
Tel: + 86 21 5257 4650
Fax: + 86 21 5208 2008
DINAMAP® PRO Series 100-400V2 Monitor Service Manual Revision B
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TABLE OF CONTENTS
Section 1. INTRODUCTION
1.1 SCOPE OF MANUAL......................................................................... 1-3
1.2 ADDENDA ..........................................................................................1-4
1.3 TRADEMARKS AND TRADE NAMES ...............................................1-4
1.4 SERVICE POLICY ..............................................................................1-4
1.5 EXTENDED WARRANTIES ...............................................................1-4
1.6 ASSISTANCE .....................................................................................1-4
1.7 SERVICE ............................................................................................1-5
Table of Contents
1.7.1 Packing Instructions .............................................................1-5
1.7.2 Insurance .............................................................................1-5
1.7.3 Replacement Assemblies and Components ........................1-5
1.7.4 Replacement Accessories ...................................................1-6
1.8 INSTALLATION AND OPERATION ...................................................1-6
1.9 WARNINGS AND PRECAUTIONS ....................................................1-6
1.10 DISPOSAL OF PRODUCT WASTE .................................................1-6
1.10.1 Batteries .............................................................................1-6
1.10.2 Patient Applied Parts .........................................................1-7
1.10.3 Packaging Material ............................................................1-7
1.10.4 Monitor ...............................................................................1-7
1.11 SYMBOL DEFINITIONS ...................................................................1-8
1.12 GLOSSARY OF TERMS AND ABBREVIATIONS ............................1-9
Section 2. PRODUCT DESCRIPTION
2.1 INTRODUCTION ................................................................................2-3
2.2 PRODUCT CONFIGURATIONS ........................................................2-3
2.3 CONTROLS, INDICATORS, AND CONNECTORS ...........................2-3
3.1 PRO Series Monitor Rear Panel Connections ........................2-4
2.3.2 Front Panel Controls and Indicators ....................................2-5
2.4 HOST PORT CONNECTOR (REAR PANEL) ....................................2-7
2.5 REORDER PART NUMBERS ............................................................2-8
2.6 SPECIFICATIONS ............................................................................2-10
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Table of Contents
Section 3. THEORY OF OPERATION
3.1 INTRODUCTION ................................................................................3-3
3.2 OVERALL PRINCIPLES OF OPERATION ........................................3-3
3.2.1 Cuff Blood Pressure (BP) and Pulse ...................................3-3
3.2.2 Temperature (Model 200 and 400) ......................................3-4
3.2.3 SpO2 (Model 300 and 400) .................................................3-4
3.2.4 Host Communication Port ....................................................3-4
3.3 FUNCTIONAL DESCRIPTION ...........................................................3-5
3.3.1 PSU PWA ............................................................................3-5
3.3.2 PSU Module .........................................................................3-5
3.3.3 Main Board ..........................................................................3-5
3.3.4 SpO2 PWA (Optional) ..........................................................3-6
3.3.5 Pneumatic Control Device ...................................................3-7
3.3.6 LCD Assembly .....................................................................3-7
3.3.7 Printer PWA w/Printer ..........................................................3-7
Section 4. GENERAL MAINTENANCE
4.1 INTRODUCTION ................................................................................4-3
4.2 FUSES ................................................................................................4-3
4.3 PERIODIC MAINTENANCE ...............................................................4-3
4.3.1 Cleaning the Monitor ............................................................4-3
4.3.2 Power-Up Checks ................................................................4-4
4.3.3 External DC Supply and Battery ..........................................4-5
4.3.4 Care of the Storage Battery .................................................4-5
4.3.5 Checking Calibration ............................................................4-6
4.4 CLINICIAN MODE...............................................................................4-6
4.4.1 Accessing the Clinician Mode ..............................................4-6
4.4.2 Clinician Mode Main Menu ..................................................4-7
4.4.3 Clinician More... Menu .........................................................4-8
4.5 SERVICE MODE ..............................................................................4-10
4.5.1 Accessing the Service Mode .............................................4-10
4.5.2 Service Mode Main Menu ..................................................4-11
4.5.3 NIBP Menu ........................................................................4-12
4.5.4 System Menu .....................................................................4-14
DINAMAP® PRO Series 100-400V2 Monitor Service Manual Revision B
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Table of Contents
4.6 PRE-SERVICE TEST PROCEDURES .............................................4-16
4.6.1 SpO2 Checks (PRO 300 & 400) ........................................4-16
4.6.2 Leak Test ...........................................................................4-18
4.6.3 NIBP Calibration Check .....................................................4-19
4.6.4 Neonate Overpressure Check ...........................................4-20
4.6.5 Adult Overpressure Check .................................................4-20
4.6.6 Temperature System Check (PRO 200 & 400) .................4-21
4.6.7 Printer Test ........................................................................4-22
4.7 PRO MONITOR CALIBRATION PROCEDURES ............................4-22
4.7.1 Calibrating the NIBP Transducer .......................................4-22
4.7.2 Overpressure Adjustment of a Two-Pot System ................4-23
4.8 ELECTRICAL SYSTEM SAFETY CHECKS .....................................4-25
4.9 FEATURES SELECTION..................................................................4-25
4.10 TROUBLESHOOTING ....................................................................4-27
4.11 ERROR CODES..............................................................................4-29
Appendix A: Test Records
Appendix B: Field Replaceable Parts and Assembly
Drawings
Appendix C: Electromagnetic Compatibility
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Table of Contents
DINAMAP® PRO Series 100-400V2 Monitor Service Manual Revision B
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1 Introduction
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Introduction
Section 1. INTRODUCTION
1.1 SCOPE OF MANUAL
This service manual provides service, parts, and repair information
and functional descriptions for the DINAMAP
®
PRO Series Monitors,
Models 100, 200, 300, and 400. The model number identifies the vital
signs monitoring capabilities built into the unit.
PRO 100: BP, pulse
PRO 200: BP, pulse, temperature
PRO 300: BP, pulse, SpO
PRO 400: BP, pulse, temperature, SpO
2
2
This manual is intended for use by biomedical engineers and trained
service technicians who are familiar with electromechanical devices
and digital and analog circuit techniques.
WARNINGS:
T o reduce the risk of electric sh ock, do not open the case. No
user-serviceable parts are inside the case. Refer servicing to
qualified service personnel.
Trained service technicians should perform all unit repairs.
Voltages dangerous to life exist in this unit. Take care when
servicing power supply and display assembly.
For information about operating PRO Series Monitors in a clinical
environment, refer to the separate operation manual.
This service manual is composed of the following five sections:
Section 1 describes this manual and tells you how to use it. Information
is also provided about how to get assistance if the unit fails to function
properly.
Section 2 provides the physical and functional char ac te rist ics of the
PRO Series Monitor.
Section 3 explains the principles of operation for the PRO Series
Monitor, including an overall system description and principles of
operation at the PWA (printed wiring board) level.
Section 4 provides information about per iod ic an d corre ct i ve
maintenance of the PRO Series Monitor. Procedures include calibration
checks, recalibration, performance tests, and fault isolation.
Section 5 provides component information about the PRO Series
Monitor, including disassembly procedures, parts lists, assembly
diagrams, and electrical schematics.
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Introduction
1.2 ADDENDA
When this manual was published it included the most up-to-date
information and procedures available. However, the specifications,
design, assembly, or software controls may change. These changes
are incorporated into this manual by addenda.
1.3 TRADEMARKS AND TRADE NAMES
This document references terms that are proprietary, and may be
registered and protected by copyrights and other applicable laws and
agreements.
The first time trademarks and trade names are used in a section of
this document, they are followed by “*” or “**”. A footnote will identify
the owner of the trademark or trade name.
1.4 SERVICE POLICY
The warranty for this product is enclosed with the product in the
shipper carton. All repairs on products under warranty must be
performed or approved by Customer Support personnel.
Unauthorized repairs will void the warranty. Products not covered by
warranty should be repaired by qualified electronics service
personnel.
1.5 EXTENDED WARRANTIES
Extended warranties may be purchased on most products. Contact
your Sales Representative for details and pricing.
1.6 ASSISTANCE
If the product fails to function properly or if assistance, service, or
spare parts are required, contact Customer Support. Before
contacting Customer Support, it is helpful to attempt to duplicate the
problem and to check all accessories to ensure that they are not the
cause of the problem. If you are unable to resolve the problem after
checking these items, contact Customer Support. When you call,
please be prepared to provide:
Product name and model number
A complete description of the problem
If repair parts or service are necessary, you will also be asked to
provide:
The product serial number
The facility's complete name and address
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1.7 SERVICE
1.7.1 Packing Instructions
Introduction
A purchase order number if the product is to be sent for repairs or
you order spare parts
The facility's GE Medical Systems Information Technologies
account number, if possible
The part number for replacement assemblies or parts
If your product requires repair service, call Customer Support and a
representative will assist you. Prior to returning any product for repair,
you must request a Return Authorization number. Call GE Medical
Systems Information Technologies at: 1-877-274-8456 Monday
through Friday, 8:00 a.m. to 6:00 p.m. EST, excluding holidays.
Follow these recommended packing instructions.
Remove the battery and all hoses, cables, sensors, and power
cords from the PRO Series Monitor before packing.
Pack only the accessories you are requested to return. Place
them in a separate bag and insert the bag and the product inside
the shipping carton.
Use the original shipping carton and packing materials, if
available.
If the original shipping carton is not available, place the product in
a plastic bag and tie or tape the bag to prevent loose particles or
materials from entering openings such as the hose ports.
Use a sturdy corrugated container to ship the product; tape
securely to seal the container for shipping.
Pack with 4 in. to 6 in. of padding on all sides of the product.
1.7.2 Insurance
Insurance is at the customer's discretion. Claims for damage to the
product must be directed to the shipper.
1.7.3 Replacement Assemblies and Components
Assemblies and components can be ordered from GE Medical
Systems Information Technologies:
Via phone: 1-800-558-7044, Option #2
Via FAX: 1-800-232-2599
Information is also available on the World Wide Web at:
http://www.gemedical.com
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Introduction
All orders must include the following information:
Facility's complete name, address, and phone number
FAX number
Your purchase order number
Your GE Medical Systems Information Technologies account
number
Please allow one working day for confirmation of your order.
1.7.4 Replacement Accessories
Replacements such as hoses, sensors, etc. must be purchased from
GE Medical Systems Information Technologies at 1-800-558-5102
(fax 1-800-232-2599). Please have the Reorder/Product Code or part
number of the item you wish to order, and your purchase order and
account number available.
1.8 INSTALLATION AND OPERATION
For information on the installation and operation of the PRO Series
Monitor, refer to the separate operation manual. The PRO Series
Monitor should be operated and serviced by authorized personnel,
and only in accordance with the warnings and precautions given in
both the operation manual and this service manual.
1.9 WARNINGS AND PRECAUTIONS
Refer to the operating safety warnings and precautions detailed in the
separate operation manual.
1.10 DISPOSAL OF PRODUCT WASTE
As you use the PRO Monitor, you will accumulate solid wastes that
require proper disposal or recycling. These include batteries, patient
applied parts, and packaging material.
1.10.1 Batteries
Caution: Do not incinerate batteries.
The sealed, rechargeable backup battery contains lead and can be
recycled. The rechargeable memory battery is of the Nickel Metal
Hydride form. Discharge this battery prior to disposal. Place the
battery in packaging which electrically isolates its contents. Do not
puncture or place the battery in a trash compactor. Do not incinerate
the battery or expose it to fire or high temperatures. Dispose in
accordance with regional body controlled guideline.
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Introduction
1.10.2 Patient Applied Parts
Certain patient applied parts, such as those with adhesive
(disposable SpO
disposed of properly as medical waste in accordance with regional
body controlled guideline.
Other patient applied parts, such as blood pressure cuffs, should be
cleaned according to instructions. Inspect reusable applied parts for
wear, replace as necessary, and dispose of used product as medical
waste in accordance with regional body controlled guideline.
1.10.3 Packaging Material
Retain original packaging materials for future use in storing or
shipping the Monitor and accessories. This recommendation includes
corrugated shippers and inserts.
Whenever possible recycle the packaging of accessories and patient
applied parts.
sensors), are intended for single use and should be
2
1.10.4 Monitor
At the end of its service life, the product described in this manual, as
well as its accessories, must be disposed of in compliance with the
guidelines regulating the disposal of such products. If you have
questions concerning disposal of the product, please contact GE
Medical Systems Information Technologies or its representatives.
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1.11 SYMBOL DEFINITIONS
Introduction
Attention: consult accompanying documents
Power ON/OFF
SILENCE
START/STOP BP
AUTO BP
Mean Arterial Pressure (MAP)
External Communications Port Connector
Defibrillator-proof Type B.F. equipment
SpO
2
BPM
IPX1
Temperature
Beats Per Minute (BPM)
Battery Power
External AC or DC Power Indicator
External DC Power Input
External AC Power Input
SpO2 Motion Artifact (US)
SpO2 Motion Artifact (Europe)
Packaging label depicting the transportation and
storage atmospheric pressure range of 500 to
1060 hPa.
The DINAMAP
against vertically falling drops of water and
conforms with the IEC 529 standard at level of
IPX1. Vertically falling drops of water shall have
no harmful effects to the Monitor.
®
PRO Series Monitor is protected
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Introduction
1.12 GLOSSARY OF TERMS AND ABBREVIATIONS
AC Alternating Current
ADC Analog to Digital Convertor
ADU Analog to Digital Units: The Main Board has 65,536 steps which
equates to 5V full scale (76 µV/ADU) Secondary Processor ADC
has 256 steps which equates to 5V full scale (19.351 mV/ADU)
AM Amplitude Modulation
ASSY Assembly
BP Blood Pressure
BPM Beats Per Minute
DC Direct Current
DMM Digital Multimeter
FET Field Effect Transistor
GAL Gate Array logic
mb Millibar
mmHg Millimeters of Mercury
HCD Host Communications Device
Hz Hertz
LCD Liquid Crystal Display
LED Light Emitting Diode
MAP Mean Arterial Pressure
NIBP Non Invasive Blood Pressure
NiMh Nickel Metal Hydride
OSC Oscillatory
PSU Power Supply Unit
PWA Printed Wiring Assembly
SPI Serial Peripheral Interface
TTL Transistor to Transistor Logic
UUT Unit Under Test
VAC Volts Alternating Current
VDC Volts Direct Current
VFC Voltage to Frequency Convertor
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Introduction
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2 Product Description
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Product Description
SECTION 2. PRODUCT DESCRIPTION
2.1 INTRODUCTION
DINAMAP® PRO Series 100-400 Monitors provide non-invasive
determination of systolic blood pressure, diastolic blood pressure,
mean arterial pressure, pulse rate, temperature, and oxygen
saturation. These portable AC and DC operated monitors are
primarily intended for use in hospital acute care settings such as
outpatient surgery, accident and emergency, labor and delivery, GI/
endoscopy, and medical/surgical units.
2.2 PRODUCT CONFIGURATIONS
Each PRO Series Monitor is supplied with an accessory pack. The
contents of the pack vary according to model. Unpack the items
carefully, and check them against the contents checklist enclosed in
one of the accessory boxes. If there is a pr oblem or shortage, contact
GE Medical Systems Information Technologies.
It is recommended that all the packaging be retained, in case the
PRO Series Monitor must be returned for service in the future.
2.3 CONTROLS, INDICATORS, AND CONNECTORS
Descriptions of the items shown are listed on the pages that follow.
For symbol definitions, refer to Section 1 of this manual.
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Product Description
2.3.1 PRO Series Monitor Rear Panel Connections
1. Battery compartment cover: Retains and protects the internal
battery.
2. Mains input: Used to connect to AC power supply.
3. External power socket: To be used with approved AC-DC power
converter ONLY.
4. Inactive temperature cable storage: Inactive temperature probe
cable attaches here (Models 200 and 400).
5. Pole clamp: Used to clamp monitor to pole or stand.
6. Data interface connector: Host communications port (15 way Dtype RS-232 serial port) for use only with equipment conforming to
IEC 601-1. Refer to section 2.4 for connection details.
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Product Description
2.3.2 Front Panel Controls and Indicators
7. Systolic pressure display: 3-digit red LED indicates measured
systolic BP in mmHg.
8. Active temperature probe holster: Temperature probe that is being
used stored here (Models 200 and 400).
9. Diastolic pressure display: 3-digit red LED indicates measured
diastolic BP in mmHg.
10. Temperature probe cover storage: Box of probe covers stored
here (Models 200 and 400).
11. Inactive temperature probe holster: Extra temperature probe
stored here (Models 200 and 400).
12. Temperature display: 4-digit red LED indicates measured
temperature (Models 200 and 400).
13. °C °F display: Indicates whether temperature is being displayed in
degrees Celsius or Fahrenheit (Models 200 and 400).
14. External power indicator: Green LED indicates external power
status and battery charging status of PRO Series Monitor.
15. Temperature probe connector: Temperature probe cable a ttaches
here (Models 200 and 400).
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Product Description
16. ON/OFF switch: Controls on/off state of PRO Monitor; push for
power on and push again for power off.
17. Battery power indicator: Yellow LED indicates operation and
charge status of battery.
18. SpO
sensor connector: SpO2 sensor extension cable attaches
2
here (Models 300 and 400).
19. Mean arterial pressure display: 3-digit red LED indicates
measured MAP in mmHg and shows instantaneous cuff pressure
during BP determination.
20. SpO
pulse indicator: Yellow LED in heart symbol flashes to
2
indicate that real-time pulse rate measurements are being derived
from SpO
signals (Models 300 and 400).
2
21. Rotor: Used to highlight and select items in LCD menus; if monitor
is off, pressing rotor will switch monitor on.
22. Pulse BPM display: 3-digit yellow LED shows pulse rate in beats
per minute.
23. SpO
display: 3-digit red LED indicates oxygen saturation in %
2
(Models 300 and 400).
24. SpO
motion/artifact indicator LED: For NELLCOR, LED
2
Illuminates when motion artifact is detected (Models 300 and 400).
For Masimo, LED illuminates when low perfusion or low signal quality
is detected (Models 300 and 400).
25. LCD (liquid crystal display): Displays all alarms, user interface
messages, and configuration options.
26. Alarm silence switch: Alternately mutes and enables audible
alarms; when pushed once after alarm sounds (silence on), the
switch illuminates to indicate that audible alarms have been silenced
for 2 minutes.
27. AUTO BP key: Press to start Auto BP mode.
28. Light sensor: Automatically measures ambient light to set LED
display intensity.
29. START/STOP BP key: Press to start or stop a BP, Auto, Stat, or
Vitals determination.
30. Cuff connector: BP cuff hose attaches here.
Not Shown: The printer access door is located on the left side of the
monitor. Push the latch to open the door and access the paper supply
and print head.
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Product Description
2.4 HOST PORT CONNECTOR (REAR PANEL)
WARNING! Auxiliary equipment connected to
the DINAMAP
®
PRO Series Monitor will result in
the formation of an electromedical system and
thus, must comply with the requirements of EN
60601-1-1/ IEC 601-1. All host port signals are
NON-ISOLATED and should be connected to
equipment conforming to IEC-601-1, configured
to comply with IEC 601-1-1 ONLY. Where
isolation of data communication is required, GE Medical Systems
Information Technologies part number ILC1926 and 683235 (Cable
Assembly) should be used. If external alarm control is required, GE
Medical Systems Information Technologies part number 487208CR
(Isolated Remote Alarm Cable Assembly) should ALWAYS be used.
Please refer to the Information Sheet included with the isolated
remote alarm cable for details.
Note: When using remote alarm, the PRO Series Monitor should be
considered the primary alarm source. The secondary alarm is used
for secondary purposes only.
Pin Assignments
Pin Function
1 Ground
2 Inverted TTL Transmit Data
3 Inverted TTL Receive Data
4 Fused +5 Volts
5 No connection
6 No connection
7 Ground
8 Remote Alarm
9 RS232 Request to Send (RTS)
10 RS232 Clear to Send (CTS)
11 RS232 Transmit Data (TxD)
12 No connection
13 RS232 Receive Data (RxD)
14 No connection
15 No connection
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2.5 REORDER PART NUMBERS
Product Product Code
DINAMAP PRO Monitor Operations Manual-English 2018548-001
DINAMAP PRO Monitor Service Manual-English 2018553-001
Battery, 12V Lead Acid 633132
Printer Paper (box of 10) 089100
DINAMAP Rolling Stand 003215
NIBP:
Air Hose 12 ft Adult/Pediatric, Screw Connector 107365
Air Hose 24 ft Adult/Pediatric, Screw Connector 107366
Air Hose 12 ft Neonatal 107368
Air Hose 12 ft Adult/Pediatric, Quick Disconnect 88847
CUFF Assortment Packs:
CLASSIC-CUF
®
Assortment Pack:
Includes: 1 each: Infant, Child Small ADult, Adult, Large Adult, Thigh Cuff
CLASSIC-CUF
®
Assortment Pack, Neonate:
Includes: 2 Neo #1, 3 Neo #2, 5 Neo #3, 5 Neo #4, 5 Neo #5
SOFT-CUF
®
Assortment Pack:
Includes: 1 Infant, 1 Child, 2 Small Adult, 2 Adult, 2 Large Adult, 1 Thigh, 1 Adult Long
SOFT-CUF
®
Assortment, Neonate:
Includes: 2 Neo #1, 3 Neo #2, 5 Neo #3, 5 Neo #4, 5 Neo #5
DURA-CUF
®
Assortment Pack:
Includes: 1 each: Infant, Child, Small Adult, Adult, Large ADult, Thigh Cuff
DURA-CUF
®
Assortment Pack, Adult:
Includes: 1 each: Infant, Child, Small Adult, Adult, Large Adult, Thigh Cuff
SENSA-CUF
TM
Assortment Pack, 2-Tube Screw Connectors: 2697
2692
2693
2695
2694
2699
2698
Includes: 1 each: Small Adult, Adult, Large Adult,
NIBP Calibration Kit 320246
Additional Blood Pressure Cuff Codes are available through: http://www.gemedical.com
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Product Description
Product Product Code
TEMPERATURE
®
TURBO TEMP Kit (contains 615118 & 2008774-001)
IVAC
®
IVAC
TURBO TEMP Oral Temp Probe, Long Cord
®
IVAC
TURBO TEMP Rectal Temp Probe, Long Cord
®
Temperature Probe Covers
IVAC
IVAC is a trademark of ALARIS Medical Systems
2011530-001
2008774-001
2008775-001
088015
SpO2:
®
NELLCOR
:
Pulse Oximeter Cable DOC-10 2008773-001
DuraSensor Adult Oxygen Sensor 407705-006
NELLCOR is a trademark of Nellcor Puritan Bennett
Masimo®:
Masimo
®
SpO2 Kit (contains 2009745-001 & 2009743-001)
2011605-001
Adult Reusable Sensor, 1/BX (NR125) 2009745-001
Cable (PC08) 2009743-001
Masimo SET® is a trademark of Masimo Corporation
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Product Description
2.6 SPECIFICATIONS
This product conforms to the essential requirements of the
Medical Device Directive. Accessories without the CE Mark are
not guaranteed to meet the Essential requirements of the
Medical Device Directive.
The PRO Series Monitor is protected against vertically falling
drops of water and conforms to the IEC 529 standard at level of
IPX1
2.6.1 Power Requirements
Mains Protection against electrical shock - Class 1
AC Input Voltage 100/240 VAC, 50/60 Hz (nominal),
Protection against electrical shock Class 1
IPX1. Vertically falling drops of water shall have no harmful
effects to the Monitor
90~253 VAC, 47~63 Hz (range),
50 VA
.
DC Input Voltage 24 VDC (nominal), 12-30 VDC, 36 VA, supplied from a source
conforming to IEC 601-1.
External DC Input Fuse AC input is protected by two internal fuses, replaceable by
qualified service personnel only. DC input line is protected by
an internal auto-resetting fuse.
Battery 12 volt, 2.3 amp-hours protected by internal auto-resetting
fuse.
Minimum operation time: 2 hrs (5 min cycle with adult cuff at
25 °C with power save mode enabled) from full charge.
Time for full recharge: 1 hr 50 min from full discharge when
the Monitor is switched off and 8 hrs when the Monitor is
switched on.
2.6.2 Environmental
Operating Temperature +5° C to +40° C (+41° F to +104° F)
Operating Atmospheric Pressure 700 hPa to 1060 hPa
Storage Temperature -20° C to +50° C (-4° F to +122° F)
Storage/Transportation Atmospheric Pressure 500 hPa to 1060 hPa
Humidity Range 0% to 95%, noncondensing
Radio Frequency Complies with IEC Publication 601-1-2 (April 1993) Medical
Electrical Equipment, Electromagnetic Compatibility
Requirements and Tests and CISPR 11 (Group 1, Class A)
for radiated and conducted emissions.
2-10 DINAMAP® PRO Series 100-400V2 Monitor Service Manual Revision B
2018553-001
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