
Revision A PRO 100 - 400 V2 Patient Monitor Service Manual
2009829-001
DINAMAP
®
PRO 100-400 Patient Monitor
Service Manual
This manual is for DINAMAP PRO Monitors 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
2
• PRO 400: BP, Pulse, Temp, and SpO
2
The model of the Monitor determines which parameters are in your monitor.
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
Technical Publications
4502 Woodland Corporate Boulevard
Tampa, FL 33614
1-877-274-8456
Part No. 2009829-001 A
The content of this document including all figures and drawings 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, Tampa, Florida.
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.
© GE Medical Systems Information Technologies 2002, TAMPA, FL 33614
Printed in the U.S.A. All rights reserved.
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