GE DINAMAP ProCare User manual

GE Healthcare
DINAMAP™ProCare Monitor
Service Manual
DINAMAP ProCare Monitor
English
2009381-001 C (paper)
© 2007 General Electric Company.
All Rights Reserved.

GE Healthcare
DINAMAP™ProCare Monitor
Service Manual
DINAMAP® ProCare Monitor Service
Manual
English
2009381-001 C (paper)
© 2007 General Electric Company.
All Rights Reserved.

T-2 DINAMAP® ProCare Monitor Service Manual 2009381-001C
February 2007
DINAMAP, CLASSIC-CUF, SOFT-CUF, AND SENSA-CUF are registered trademarks of GE Medical Systems Information
Technologies. GE is a registered trademark of General Electric Company. All other product and brand names are
trademarks or registered trademarks of their respective companies. ©2005, 2006 GE Medical Systems Information
Technologies. All rights reserved. No part of this manual may be reproduced without the permission of GE Medical
Systems Information Technologies.
GUARANTEE
All equipment sold by GE Medical Systems Information Technologies, is fully guaranteed as to
materials and workmanship for a specified period. Refer to your warranty for more
information. GE Medical Systems Information Technologies reserves the right to perform
guarantee service operations in its own factory, at an authorized repair station, or in the
customer’s installation.
Our obligation under this guarantee is limited to repairing, or, at our option, replacing any
defective parts of our equipment, except fuses or batteries, without charge, if such defects
occur in normal service.
Claims for damage in shipment should be filed promptly with the transportation company. All
correspondence covering the instrument should specify the model and serial numbers.
GE MEDICAL SYSTEMS Information Technologies
A GE Healthcare Company
NOTE: In addition to software version RAI, the information in this manual also applies to earlier DINAMAP® ProCare
Monitor Service Manual software versions. There are no user-apparent differences among these software versions.
Due to continuing product innovation, specifications in this manual are subject to change without notice.
GE Medical Systems Information Technologies will make available on request such circuit
diagrams, component diagrams, component parts lists, descriptions, calibration instructions,
or other information which will assist the users or appropriately qualified technical personnel
to repair those parts of the equipment which are classified by GE Medical Systems Information
Technologies as repairable.
CAUTION: In the United States of America, Federal Law restricts this
device to sale by or on the order of a physician.
MASIMO SET®is a trademark of Masimo Corporation. Possession or purchase of this device
does not convey any express or implied license to use the device with replacement parts which
would, alone, or in combination with this device, fall within the scope of one or more of the
patents relating to the device.
NELLCOR®, OxiMax®, OxiCliq®,and SatSeconds™ are trademarks of Nellcor Puritan Bennett.
IVAC®and TURBO
 TEMP®are trademarks of ALARIS Medical Systems

Revision C DINAMAP® ProCare Monitor Service Manual i
2009381-001
1Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1
Revision History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
Manual Purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
Ordering Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
Safety Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
Responsibility of the Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-4
General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-4
References to Persons, Places, and Institutions . . . . . . . . . . . . . . . . . . . . . .1-4
Warnings, Cautions, and Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-5
Product Specific Hazards . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-5
Warnings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-5
Cautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-6
Equipment Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
Service Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8
Equipment ID . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8
Intended Audience . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8
Intended Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-9
General Use . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-9
Related Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-9
Service Policy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-9
Service Contracts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-9
Assistance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-9
Service . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-10
Packing Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-10
Insurance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-10
Service No Charge Rental . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-10
Repair Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-11
Disposal of Product Waste . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-11
Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-11
Patient Applied Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-11
Packaging Material . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-12
Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-12
2Equipment Overview . . . . . . . . . . . . . . . . . . . . . . . . . 2-1
Equipment Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
Product Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3

ii DINAMAP® ProCare Monitor Service Manual Revision C
2009381-001
Basic Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-4
Front Panel Controls and Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-4
Buttons . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-4
Front Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-5
Product Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Theory of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8
Overall Principles of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
SpO2 (Model 300 and 400) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-9
Cuff Blood Pressure (BP) and Pulse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-9
Principles of Noninvasive Blood Pressure Determination . . . . . . . . .2-9
Systolic Search . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
Reference Used to Determine NIBP Accuracy . . . . . . . . . . . . . 2-11
DINAMAP®Monitors With Intra-Arterial Reference
(DINAMAP®Classic Technology) . . . . . . . . . . . . . . . . . . . . . . 2-11
DINAMAP®Monitors With Auscultatory Reference
(DINAMAP®Auscultatory Technology) . . . . . . . . . . . . . . . . 2-11
Temperature (Model 200 and 400) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
Host Communication Port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
Functional Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
Main Board PWA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
User Interface (UI) Board PWA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
SPO2PWA . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
Printer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
Pneumatic Valve/Manifold (PVM) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
Optical Switch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
3Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
Rear Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-3
Right-Side Panel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-3
Powering the Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-4
Power Sources . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-4
Battery Charging . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-4
Unpacking and Preparation for Installation . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Configuring Your ProCare Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
Operating Modes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-6
Clinical Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-6
Configuration Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-6
Configuration Mode Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
Setting the Date and Time . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-7

Revision C DINAMAP® ProCare Monitor Service Manual iii
2009381-001
Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-7
Inflation Pressure Default Setting . . . . . . . . . . . . . . . . . . . . . . .3-8
Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-8
Alarm Default Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-8
Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-8
SPO2 Configuration Settings . . . . . . . . . . . . . . . . . . . . . . . . . . .3-8
Procedure for units with Nellcor®Technology . . . . . . . . . . .3-8
Procedure for units with Masimo®Technology . .3-9
Advanced Configuration Mode . . . . . . . . . . . . . . . . .3-9
Service Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-11
Host Communications Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13
DB15 Connector Pin Assignments . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13
Connection Details . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13
Host Port Connector (rear panel) . . . . . . . . . . . . . . . . . . . . . . . . . . 3-13
4Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1
Preventative Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-3
Integrity of Hoses and Cuffs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-3
Visual Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
Cleaning the Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-4
Cleaning Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-4
Monitor Exterior . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-4
Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-5
Cuffs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-5
General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Materials . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Temperature Devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-6
SpO2Sensors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-6
Long-Term Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
Battery Care . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-7
Replacing the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-8
Fuses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-9
Parameter Level Functional Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9
BP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-9
Temperature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-9
Nellcor SpO2 Technology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-9
Masimo SpO2 Technology . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-9
Calibration Procedures and Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Annual Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10

iv DINAMAP® ProCare Monitor Service Manual Revision C
2009381-001
Parameter Test Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Leakage Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
Pressure Transducer Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12
Pressure Transducer Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12
Overpressure Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-13
Button Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-13
LED Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-13
External DC Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-14
BP Determination . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-14
BP Overpressure Verification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-14
Temperature (Perform if equipped with Temp module) . . . . . . . . . 4-14
SpO2 (Perform only if equipped with SpO2 module) . . . . . . . . . . . . 4-16
Printer Output Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-16
Temp Circuit Leakage Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-16
SpO2 Circuit Leakage Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-16
Test Results Form . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-17
5Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1
Alarm Code Interpretation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
System Failures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-3
Alarm Conditions and Error Codes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-3
Error Log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-3
Procedure to View and Print Error Code History Log: . . . . . . . . . . . . .5-3
6Parts List, Drawings, and Replacement . . . . . . . . . 6-1
Ordering Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3
Service Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3
Compatible Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-3
Field-Replaceable Units (FRUs) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-6
FRU List . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-6
FRU Main Reference Guide Drawing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-16
Assembly/Disassembly of FRUs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-17
Monitor Disassembly Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-17
Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-17
Rear Case . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-17
Printer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-18
SpO2 Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-20
Main Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-20
Display Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-21

Revision C DINAMAP® ProCare Monitor Service Manual v
2009381-001
ATechnical Specifications . . . . . . . . . . . . . . . . . . . . . . A-1
Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-3
Mechanical . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-3
Power Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-3
Environmental . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-4
BP . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-4
Factory Default Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-4
Critikon US Patents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-5
European Patents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-5
Nellcor SpO2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-5
Measurement Range . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-5
Accuracy and Motion Tolerance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-5
Saturation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-5
Pulse Rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-5
NELLCOR®Sensor Accuracy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-6
OxiMax®. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-6
OxiCliq®. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-6
Reusable Sensor Models . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-6
Neonatal Sensor Accuracy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-6
Sensor Light Source . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-6
Factory Default Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-7
NELLCOR®Patents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-7
Masimo SpO2. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-7
Measurement Range . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-7
Accuracy and Motion Tolerance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-7
Saturation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-7
Pulse Rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-7
Masimo® Sensor Accuracy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-8
Resolution . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-8
Low Perfusion Performance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-8
Interfering Substances . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-8
Sensor Light Source . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-8
Factory Default Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-8
Masimo Patents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-8
Temperature . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-9
Factory Default Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-9
IVAC®Patents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-9
Pulse Rate . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-9
Factory Default Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-9

vi DINAMAP® ProCare Monitor Service Manual Revision C
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BAppropriate Use of NIBP Simulators . . . . . . . . . . . . B-1
Appropriate Use of NIBP Simulators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-3
NIBP Accuracy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-3
Clinical vs. Simulator Readings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-3
What Do Simulator Manufactures Say? . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-4
Why Use Simulators? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-5
Summary . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-5
CElectromagnetic Compatibility (EMC) . . . . . . . . . . . C-1
Electromagnetic Compatibility (EMC): ProCare Monitor . . . . . . . . . . . . . . C-3
Guidance and Manufacturer’s Declaration –
Electromagnetic Emissions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-3
Guidance and Manufacturer’s Declaration –
Electromagnetic Immunity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-4
Recommended Separation Distances . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-6
Compliant Cables and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-7
Electromagnetic Compatibility (EMC): ILC-1926 . . . . . . . . . . . . . . . . . . . . . C-8
Guidance and Manufacturer’s Declaration –
Electromagnetic Emissions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-8
Guidance and Manufacturer’s Declaration –
Electromagnetic Immunity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-9
Recommended Separation Distances . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-11
Compliant Cables and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-12
Electromagnetic Compatibility (EMC): ILC-1931 . . . . . . . . . . . . . . . . . . . . C-13
Guidance and Manufacturer’s Declaration –
Electromagnetic Emissions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-13
Guidance and Manufacturer’s Declaration –
Electromagnetic Immunity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-14
Recommended Separation Distances . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-16
Compliant Cables and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-17

Revision C DINAMAP® ProCare Monitor Service Manual 1-1
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1Introduction

1-2 DINAMAP® ProCare Monitor Service Manual Revision C
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For your notes

Revision C DINAMAP® ProCare Monitor Service Manual 1-3
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Introduction: Revision History
Revision History
Each page of this manual has a revision letter located at the bottom of the page.
This letter identifies the revision level of the entire manual. This may be important
if you have different manuals and you do not know which is the most current.
For the initial release, all pages have the revision letter A. For the second update,
all pages receive the revision letter B. The latest letter of the alphabet added to
the table below corresponds to the most current revision.
Manual Purpose
This manual supplies technical information for service representatives and
technical personnel so they can maintain the equipment to the assembly level.
Use it as a guide for maintenance and electrical repairs considered field
repairable. Where necessary the manual identifies additional sources of relevant
information and technical assistance. See the operator's manual for the
instructions necessary to operate the equipment safely in accordance with its
function and intended use.
Ordering Manuals
A paper copy of this manual will be provided upon request. Contact your local GE
representative and request the part number on the first page of the manual.
Safety Information
The information presented in this section is important for the safety of both the
patient and operator. This chapter describes how the terms Danger, Warning,
Caution, Important, and Note are used throughout the manual. In addition,
standard equipment symbols are defined.
Revision Date Comment
A30-April-2002 Initial Release
B01-October-2004 Add EMC Compliance Testing Tables
C05-February-2007 Update specifications, tests, FRU
drawings, FRU lists, format, and add
error log feature info.

1-4 DINAMAP® ProCare Monitor Service Manual Revision C
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Introduction: Safety Information
Responsibility of the Manufacturer
GE is responsible for the effects on safety, reliability, and performance only if:
assembly operations, extensions, readjustments, modifications, or repairs
are carried out by persons authorized by GE;
the electrical installation of the relevant room complies with the
requirements of appropriate regulations; and
the monitor is used in accordance with the instructions of use.
General
This device is intended for use under the direct supervision of a licensed health
care practitioner.
This device is not intended for home use. Federal law restricts this device to be
sold by or on the order of a physician.
Contact GE for information before connecting any devices to the equipment that
are not recommended in this manual.
Parts and accessories used must meet the requirements of the applicable IEC/
EN 60601 series safety standards, and/or the system configuration must meet
the requirements of the IEC 60601-1-1 medical electrical systems standard.
Periodically, and whenever the integrity of the device is in doubt, test all
functions.
The use of ACCESSORY equipment not complying with the equivalent safety
requirements of this equipment may lead to a reduced level of safety of the
resulting system. Consideration relating to the choice shall include:
use of the accessory in the PATIENT VICINITY; and
evidence that the safety certification of the ACCESSORY has been performed
in accordance to the appropriate IEC 60601-1 and/or IEC 60601-1-1
harmonized national standard.
If the installation of the equipment, in the USA, will use 240V rather than 120V,
the source must be a center-tapped, 240V, single-phase circuit.
References to Persons, Places, and Institutions
References to persons, places, and institutions used within this manual are solely
intended to facilitate user comprehension of the ProCare Monitor Monitor’s use
and functions. Extreme care has been taken to use fictitious names and related
information in the examples and illustrations provided herein. Any similarity of
this data to persons either living or dead and to either current or previously
existing medical institutions should be regarded as coincidental.

Revision C DINAMAP® ProCare Monitor Service Manual 1-5
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Introduction: Safety Information
Warnings, Cautions, and Notes
The terms danger, warning, and caution are used throughout this manual to
point out hazards and to designate a degree or level or seriousness. Familiarize
yourself with their definitions and significance. Hazard is defined as a source of
potential injury to a person.
DANGER indicates an imminent hazard which, if not avoided, will result in death
or serious injury.
WARNING indicates a potential hazard or unsafe practice which, if not avoided,
could result in death or serious injury.
CAUTION indicates a potential hazard or unsafe practice which, if not avoided,
could result in minor personal injury or product/property damage.
NOTE provides application tips or other useful information to assure that you get
the most from your equipment.
Product Specific Hazards
Warnings
Do not use the ProCare Monitor in the presence of magnetic resonance
imaging (MRI) devices. There have been reports of sensors causing patient
burns when operating in an MRI environment.
Do not use the Monitor in the presence of flammable anesthetics.
To help prevent unintended current return paths with the use of high
frequency (HF) surgical equipment, ensure that the HF surgical neutral
electrode is properly connected.
 To avoid personal injury, do not perform any servicing unless qualified to do so.
WARNING: These Monitors should not be used on patients who are
connected to cardiopulmonary bypass machines.
If powering the Monitor from an external power adapter or converter, use
only GE Medical Systems Information Technologies-approved power
adapters and converters.
The Monitor does not include any user-replaceable fuses. Refer servicing to
qualified service personnel.
To reduce the risk of electric shock, do not remove the cover or the back.
Refer servicing to a qualified service person.
If the accuracy of any determination reading is questionable, first check the
patient’s vital signs by alternate means and then check the ProCare Monitor
for proper functioning.
Use of portable phones or other radio frequency (RF) emitting equipment
near the system may cause unexpected or adverse operation.
The equipment or system should not be used adjacent to, or stacked with,
other equipment. If adjacent or stacked use is necessary, the equipment or
system should be tested to verify normal operation in the configuration in
which it is being used.
The use of accessories, transducers and cables other than those specified
may result in increased emissions or decreased immunity performance of
the equipment or system.

1-6 DINAMAP® ProCare Monitor Service Manual Revision C
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Introduction: Equipment Symbols
Cautions
Do not use replacement batteries other than the type supplied with the
Monitor. Replacement batteries are available from GE Medical Systems -
Accessories and Supplies.
The ProCare Monitor is designed to conform to Electromagnetic
Compatibility (EMC) standard IEC 601-1-2, 1993 and will operate accurately
in conjunction with other medical equipment which also meets this
requirement. To avoid interference problems affecting the Monitor, do not
use the Monitor in the presence of equipment which does not conform to
these specifications.
Place the ProCare Monitor on a rigid, secure surface. Monitor must only be
used with mounting hardware, poles, and stands recommended by GE
Medical Systems Information Technologies.
The weight of the accessory basket contents should not exceed 5 lb (2.7kg).
Arrange the external AC/DC power converter, air hoses, and all cables
carefully so they do not constitute a hazard.
Verify calibration of BP parameter (temp and pulse oximeter do not require
calibration). Ensure that the display is functioning properly before operating
the ProCare Monitor.
Do not immerse the Monitor in water. If the Monitor is splashed with water or
becomes wet, wipe it immediately with a dry cloth.
Do not gas sterilize or autoclave.
The ProCare Monitor, when used with GE Medical Systems Information
Technologies-approved applied parts and accessories, is protected against
defibrillator damage.
NOTE: The electromagnetic compatibility profile of the ProCare Monitor may
change if accessories other than those specified for use with the
ProCare Monitor are used.
Equipment Symbols
The following symbols are associated with the ProCare Monitor. Some of the
symbols may not appear on all equipment.
NOTE: The model of the Monitor determines which symbols appear on it.
Attention, consult accompanying documents
Silence
Alarms
+ / -
Menu

Revision C DINAMAP® ProCare Monitor Service Manual 1-7
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Introduction: Equipment Symbols
Inflate/Stop
Cycle
History
Print
On/Off
Battery Power
External Communications Port Connector
Charging
Defibrillator-proof type BF equipment
External AC or DC power indicator
Class II equipment according to IEC 60536
Packaging label depicting the transportation and storage
atmospheric pressure range of 500 to 1060 hPa.
WASTE OF ELECTRICAL AND ELECTRONIC EQUIPMENT
(WEEE): This symbol indicates that the waste of
electrical and electronic equipment must not be
disposed as unsorted municipal waste and must be
collected separately. Please contact an authorized
representative of the manufacturer for information
concerning the decommissioning of your equipment.
The DINAMAP®ProCare Monitor is protected against
vertically falling drops of water and conforms with the
IEC 529 standard at level of IPX1. Vertically falling drops
shall have no harmful effects to the Monitor.
IPX1

1-8 DINAMAP® ProCare Monitor Service Manual Revision C
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Introduction: Service Requirements
Service Requirements
Follow the service requirements listed below.
Refer equipment servicing to GE Medical Systems Information Technologies
authorized service personnel only.
Any unauthorized attempt to repair equipment under warranty voids that
warranty.
It is the user’s responsibility to report the need for service to GE Medical
Systems Information Technologies or to one of GE’s authorized agents.
Failure on the part of the responsible individual, hospital or institution using
this equipment to implement a satisfactory maintenance schedule may
cause undue equipment failure and possible health hazards.
Regular maintenance, irrespective of usage, is essential to ensure that the
equipment will always be functional when required.
Equipment ID
The following graphic illustrates the components of the monitor’s serial number.
Intended Audience
This manual is intended for service representatives and technical personnel who
maintain, troubleshoot, or repair this equipment.
GEMS IT Global Serial Number Format
13- Digit
# # # # # # # # # # # # #
3-character product code
Year
Fiscal week
Sequential serial number (up to 9999)
Manufacturing site
Misc. : Prototype, refurbish, etc.

Revision C DINAMAP® ProCare Monitor Service Manual 1-9
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Introduction: Service Policy
Intended Use
General Use
The ProCare Monitor is intended to monitor one patient at a time in a clinical
setting.
Federal law (U.S.A.) restricts this device to sale by or on the order of a
physician.
To ensure patient safety, use only parts and accessories manufactured or
recommended by GE Medical Systems Information Technologies. Parts and
accessories used shall meet the requirements of EN60601.1.1.
Disposable devices are intended for single use only. They should not be
reused.
Periodically, and whenever the integrity of the monitor is in doubt, test all
functions.
Related Manuals
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
Product Service personnel. Unauthorized repairs will void the warranty. Only
qualified electronics service personnel should repair products not covered by
warranty.
Service Contracts
Extended warranties can be purchased on most products. Contact your Sales
Representative for details and pricing.
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 GE Medical Systems Information
Technologies. Prior to calling, please be prepared to provide:
product name, model number, and serial number
a complete description of the problem
Manual Title
2009360-001 DINAMAP ProCare Operation Manual

1-10 DINAMAP® ProCare Monitor Service Manual Revision C
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Introduction: Service Policy
If repair parts or service are necessary, you will also be asked to provide:
the product serial number
the facility's complete name, address, and account number
a purchase order number if the product is to need of repair or when you
order spare parts
the facility's GE Medical Systems Information Technologies account number,
if possible
the appropriate part number for spare or replacement parts
Service
If your product requires warranty, extended warranty or non-warranty repair
service, call Customer Support and a representative will assist you. To facilitate
prompt service in cases where the product has external chassis or case
damage, please advise the Customer Support representative when you call.
The Customer Support representative will record all necessary information and
will provide you with a Return Merchandise Authorization Number (RMA). Prior to
returning any product for repair, you must have a RMA number. Contact GE
Medical Systems Information Technologies at 1-800-558-7044.
Monday through Friday, 8:00 a.m. to 6:00 p.m. EST, excluding holidays.
Packing Instructions
Follow these recommended packing instructions.
Remove all hoses, cables, sensors, and power cords from the 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 hose ports.
Use a sturdy corrugated container to ship the product; tape securely to seal
the container for shipping.
Pack with 4 to 6 in. of padding on all sides of the product.
Insurance
Insurance is at the customer's discretion. The shipper must initiate claims for
damage to the product.
Service No Charge Rental
A no charge rental unit is provided at no charge during the warranty period of
the product when we perform the repair service.
GE Medical Systems Information Technologies pays the shipping charges for
a loaner sent to the customer for product repairs under the warranty.