GE Dash 2500

GE Healthcare
Dash 2500 Patient Monitor

Service Manual

English
2042481-001 C (paper)
2042482-001 C (CD)
2009 General Electric Company.
All Rights Reserved.
GE Healthcare

Service Manual

English
2042481-001 C (paper)
2042482-001 C (CD)
2009 General Electric Company.
All Rights Reserved.
NOTE: In addition to software version RAJ, the information in this manual also applies to the old Dash 2500 Patient
Monitor software version . 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.
NOTE: For technical documentation purposes, the abbreviation GE is used for the legal entity name, GE Medical
Systems Information Technologies.
Listed below are GE Medical Systems Information Technologies trademarks. All other trademarks contained herein are the
property of their respective owners.
Ohmeda Oximetry and other trademarks (OxyTip+, PIr, TruSat, TruSignal, TruTrak+) are the property of GE Medical Systems
Information Technologies, a division of General Electric Corporation. All other product and company names are the
property of their respective owners.
Alaris Turbo Temp is a trademark of ALARIS Medical Systems.
SuperSTAT, Trim Knob and EK-Pro are registered trademarks of GE Medical Systems Information Technologies.
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, C-LOCK and SatSeconds are trademarks of Nellcor Puritan Bennett.
T-2
2042481-001 C
Jan. 2009
Contents
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1
Manual Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
Revision History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
Manual Purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
Intended Audience . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
Ordering Manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
Illustrations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-4
Safety Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4
Responsibility of the Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-4
General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-4
Warnings, Cautions, and Notes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-5
Equipment Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-6
Service Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-8
Service Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-8
Equipment Identification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-8
Equipment Overview . . . . . . . . . . . . . . . . . . . . . . . . . 2-1

Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
Equipment Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3
Configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3
Controls and Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-4
Theory Of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
NELLCOR SpO2 and MASIMO SET SpO2 . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6
DINAMAP Blood Pressure and Pulse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7
Alaris Oral and Rectal TURBO TEMP Thermometry . . . . . . . . . . . . . . . . .2-7
ECG with Heart Rate and Respiration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7
Host Communication Port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8
Communication Adaptor Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8
DB15 / DB9 Connector Pin Assignments . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-9
Functional Description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
System Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-16
3
Revision C
Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3
Dash 2500 Patient Monitor Service Manual

2042481-001
Rear Panel Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-3

Power Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-3
Set Up/Configure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Setting up the Dash 2500 Monitor for the First Time . . . . . . . . . . . . . . . . . .3-4
Configure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-5
Mounting Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-5
Software Upgrade . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-5
Network set up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-5
Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1
Maintenance Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Manufacturer Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-3
Manufacturer Responsibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-3
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-4
Periodic Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
Integrity of Hoses and Cuffs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-6
Long-Term Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-6
Periodic Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-6
Care of Storage Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-7
Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-8
General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-8
Test Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-8
Safety Resistance Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-8
Patient (Source) Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Patient (Sink) Leakage Current Testing
(Mains Voltage on the Applied Part) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12
Checkout Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Parameter Level Functional Testing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Service Mode Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Service Mode Exit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
4-13
4-13
4-14
4-31
Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1
Required Service Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
General Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Parameter Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-5
Error Codes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-6
Alarm Code Interpretation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-6
System Failures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-6
ii

2042481-001
Revision C
Field Replaceable Units . . . . . . . . . . . . . . . . . . . . . . . 6-1

Ordering Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3
Parts . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-4
Assembly Drawings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-6
Disassembly Guidelines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Tools Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Before Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Hardware Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Electrostatic Discharge (ESD) Precautions . . . . . . . . . . . . . . . . . . . . . . . . .
6-14
6-14
6-14
6-15
6-15
Remove/Replace Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-16

Replace Plastic Front Case . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-17
Replace Main Board Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-18
Replace DAS Board Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-19
Replace DC2DC Board Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-20
Replace AC2DC Board Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-21
Replace Keyboard and Trim Knob . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-22
Replace the Invert Board . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-23
Replace the AC Inlet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-24
Replace the Speaker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-25
Replace the printer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-25
Replace the Pneumatic Pump . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-26
Replace the Check Valve . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-26
Replace the Fan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-27
Assemble Network Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-28
After Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-29
Technical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . .A-1

Technical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-3
General Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A-3
NIBP Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A-5
GE Healthcare Patents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A-5
NELLCOR Puritan Bennett, Inc. Patents . . . . . . . . . . . . . . . . . . . . . . . . . . . .A-7
MASIMO SET SpO2 Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A-8
MASIMO Patents . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A-9
ECG Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-10
Revision C

2042481-001
iii
RESP Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-11

HR/Pulse Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-12
TURBO TEMP Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-13
B
C
Test Record . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .B-1
Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .C-1
Monitor Configuration Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Enter Configuration Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Configure Default Changes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
Exit Configuration Mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .
C-3
C-3
C-3
C-4
Auxiliary Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-1

Auxiliary Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . D-3
EMC Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .E-1

Electromagnetic Compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . E-3
Guidance and Manufacturers Declaration
Electromagnetic Emissions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .E-3
Electromagnetic Immunity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .E-4
Electromagnetic Immunity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .E-5
Recommended Separation Distances . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .E-6
Compliant Cables and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .E-7
Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-1
Technical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-3
Product Compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .F-3
External Connectors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-4
Ethernet Port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .F-4
iv

2042481-001
Revision C
Service Port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .F-5

LEDs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .F-6
Communication Adaptor Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-7
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-8
Installation Configuration Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-8
Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .F-8
Boot Service Menus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-11
Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-11
Using the Boot Service Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-12
Service Menus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-14
Preparation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-14
Using the Service Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . F-15
Revision C

2042481-001
vi

2042481-001
Revision C
Revision C
Introduction

2042481-001
1-1
For your notes
1-2

2042481-001
Revision C
Introduction: Manual Information
Manual Information
Revision History
Each page of this manual has the document part number and revision letter at
the bottom of the page. The revision letter identifies the documents update
level. The revision history of this document is summarized below.
Revision
Comment
Initial release of the manual
ECO release
ECO release
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 operators manual for the instructions necessary to operate the
equipment safely in accordance with its function and intended use.
Intended Audience
This manual is intended for service representatives and technical personnel who
maintain, troubleshoot, or repair this equipment.
Ordering Manuals
To order additional copies of this manual, call Accessories and Supplies and
request part number 2042481-001 for a paper copy, and 2042482-001 for a CD
copy. Refer to the How To Reach Us page for Accessories and Supplies contact
information.
WARNING
This Service Manual is available in English only except as
otherwise expressly required by local law or agreed to at a
local level.
If a customers service provider requires a language other
than English, it is the customers responsibility to provide
translation services.
Do not attempt to service the equipment unless this
Service Manual has been consulted and is understood.
Failure to heed this Warning may result in injury to the
Revision C

2042481-001
1-3
Introduction: Safety Information

service provider, operator or patient from electric shock,
mechanical or other hazards
Illustrations
All illustrations in this manual are only examples, and may not necessarily
reflect your system settings or data displayed in your system. If a particular
selection is not available in your system, the selection is shown grayed in the
menu.
Safety Information
Responsibility of the Manufacturer
GE is responsible for the effects of 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 the appropriate regulations.
The equipment is used in accordance with the instructions for 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
601 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 606011-1 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.
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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 imminently hazardous situation, which, if not avoided, will
result in death or serious injury. Methods to avoid the hazard should be included.
This signal word is to be limited to the most extreme situation. This signal word
shall not be used to indicate incidents resulting in property damage only.
WARNING indicates a potentially hazardous situation, which, if not avoided,
could result in death or serious injury. This includes serious adverse reactions, or
limitations in use. Steps that should be taken to avoid or minimize the hazard
should be included.
This signal word is not to be used to indicate incidents resulting in property
damage only.
CAUTION indicates a potentially hazardous situation, which, if not avoided, may
result in minor or moderate injury.
It may also be used to alert against unsafe practices or to describe
recommended. This signal word may be used to indicate incidents resulting in
potential property damage only. Practices for the safe and effective use of the
device.
NOTE shall be used for informational messages that do not pertain to a hazard.
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Introduction: Equipment Symbols
Equipment Symbols
NOTE: Some symbols may not appear on all equipment.
ATTENTION: Consult accompanying documents before using the equipment.
Defibrillator-proof type CF equipment; type CF equipment is specifically

designed for applications where a conductive connection directly to the heart
is established. The paddles indicate the equipment is defibrillator proof.
Defibrillator-proof type BF equipment; type BF equipment is suitable for
intentional external and internal application to the patient, excluding direct
cardiac application. Type BF equipment is type B equipment with an F-type
isolated (floating) part. The paddles indicate the equipment is defibrillator
proof.
Temperature
Potential Equalization Terminal: Terminal for providing a connection

between the equipment and the potential equalization busbar of the
electrical installation.
Alternating current (AC)
Battery in use
Storage temperature
Packaging label depicting the transportation and storage atmospheric

pressure range of 500 to 1060 hPa.
This side up
Keep dry
Fragile, handle with care
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Introduction: Equipment Symbols
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 separate collection symbol is affixed to a battery, or its packaging, to
advise you that the battery must be recycled or disposed of in accordance
with local or country laws. To minimize potential effects on the
environment and human health, it is important that all marked batteries
that you remove from the product are properly recycled or disposed. For
information on how the battery may be safely removed from the device,
please consult the service manual or equipment instructions. Information
on the potential effects on the environment and human health of the
substances used in batteries is available at this url:
http://www.gehealthcare.com/euen/weee-recycling/index.html
Manufacturer: This symbol is acompanied by the name and the address of the
manufactuer.
Manufacturing Date: This symbol is acompanied by the date of the

manufacturing.
This product consists of devices that may contain mercury, which must be
recycled or disposed of in accordance with local, state, or country laws. (Within
this system, the backlight lamps in the monitor display contain mercury.)
This product get an Nationally Recognzied Testing Laboratory (NRTL) approve
based on United States standard UL 60601-1:2003 and Canada standard CAN/
CSA-C22.2 No. 601.1-M90.
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Introduction: Service Information
Service Information
Service Requirements
Follow the service requirements listed below.
Refer equipment servicing to GE-authorized service personnel only.
Any unauthorized attempt to repair equipment under warranty voids that

warranty.
It is the users responsibility to report the need for service to GE or to one of

their 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 Identification
Every GE device has a unique serial number for identification. A sample of the
information found on a serial number label is shown below.
### ## ## #### # #
Description
A
product code1
year manufactured
fiscal week manufactured
production sequence number
manufacturing site
miscellaneous characteristic
1. Current Dash monitor product code SCG
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Equipment Overview

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For your notes
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Equipment Overview: Components
Components
Equipment Description
The Dash 2500 patient monitor is intended to monitor and measure oscillometric
noninvasive blood pressure (systolic, diastolic, and mean blood pressure), heart
rate/pulse, respiration rate, ECG with lethal arrhythmia (VTACH, VFIB/VTACH, and
asystole), oxygen saturation (SpO2) by noninvasive pulse oximetry, and
predictive temperature with an electronic thermometer for adult, pediatric and
neonatal patients. The Dash 2500 Monitor also detects alarm limit conditions
and is capable of recording up to two waveforms. Using this Monitor, a clinician
can view, record, and recall clinical data derived from each parameter.
The Dash 2500 can be configured with or without a printer and/or temperature
module. Also, the units are ordered with either Masimo or Nellcor SpO2.
The network function is optional for Dash 2500.
Configurations
Each 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
checklists enclosed within the accessory boxes. If an accessory is missing or if
an item is in a nonworking condition, contact GE Medical Systems Information
Technologies immediately.
NOTE: Perform regular functional testing of each of the parameters, using the
accessories supplied with the Dash 2500 Monitor.
It is recommended that all the packaging be retained, in case the Monitor must
be returned for service in the future.
Controls and Indicators

Descriptions of the items shown are listed on the pages that follow. Refer to
Chapter 1 Introduction for symbol definitions.
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Equipment Overview: Controls and Indicators
Monitor
AC Power Indicator
The indicator lights green when AC mains power is applied to the Monitor. The
indicator does not illuminate when the Monitor has no AC mains power.
Battery Power Indicator

The indicator lights yellow when the Monitor is operating on battery power. The
indicator does not illuminate when the Monitor has no battery power. The
battery indicator is in the front panel of the Monitor.
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Equipment Overview: Controls and Indicators
Front Panel Controls

NIBP Go/Stop - starts and stops any determination of noninvasive blood
pressure.
NIBP Auto - is a dual-function hardkey. Starts auto BP determinations by a
single-press and gives you access to change the NIBP cycle time.Starts stat
determinations pressing and holding the key down (5 minutes of continuous
NIBP cycles).
Zero - zeros the IBP determination.This hardkey is available only for use when
IBP is configured.IBP is not configured in Dash 2500.
Silence Alarm - temporarily silences alarms; acknowledges alarming crisis

conditions.
Power - turns Monitor off and on.
Print - prints a snapshot (timed recording) with a single-press. Pressing and

holding the key down allows for a continuous recording of the chosen
waveforms.
Freeze - captures up to 16.8 seconds of waveforms on the screen. The number
of seconds varies depending on the selected sweep speed.
Trend - enters and exits trends (view patient trends data). This hardkey can be
configured through the configuration mode to display two different views: mini
trends or full trends.
Standby - enters and exits standby mode.
Main - closes the menu system and takes you back to the main screen.
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Equipment Overview: Theory Of Operation
Theory Of Operation
The Monitor is a portable unit that receives input power from an external AC
source, or internal rechargeable battery.
When the Power button is pressed, the Main Board is brought out of a sleep
mode and turns on the power regulators. The power regulators provide
conditioned power from one of the two input power sources:
AC Mains
Internal battery
Once the Monitor is energized, a self-test is performed. The self-test

automatically tests the main functions of the Monitor. Failure of the self-test sets
the Monitor into a fail-safe mode with an audio alarm. Under normal operating
condition, the Monitor is ready to monitor the patient's vital signs using four
external attachments:
Temperature probe for either rectal or oral use
SpO2 sensor
ECG leads
Cuff
Interface with a central station or other device is accomplished through the 9pin host communication port or the 15-pin wireless communication port on the
back of the Monitor.
NELLCOR SpO2 and MASIMO SET SpO2

When the SpO2 sensor is attached to the SpO2 connector and to the patient, it
senses both the pulse rate and oxygen saturation. These analog signals are
routed to and analyzed by the SpO2 PWA. The results are digitized and sent to
the DAS Board, and DAS repacks and sends them to Main Board through the
opto couplers. The couplers provide for patient isolation as well as serial data
interface. The Main Board routes the data to the appropriate screen displays
and/or printer.
A reset signal to the SpO2 PWA is also provided for power up sequencing.
NELLCOR IS TRADEMARK OF NELLCOR PURITAN BENNETT INC.

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.
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DINAMAP Blood Pressure and Pulse

When the cuff and hose are attached to the Monitor and Non-Invasive Blood
Pressure (NIBP) determination is initiated, the pump inflates the cuff. The
pressure transducers (PT1 and PT2) monitor pressure information. The
pneumatic manifold has two valves, which are used to deflate the cuff. Valve
control is through the Main Board. Determinations are made for the systolic BP,
diastolic BP, pulse rate, and Mean Arterial Pressure (MAP). The results are
displayed on the Monitor's front panel Liquid Crystal Display (LCD) screen.
If an over-inflation condition occurs, it is detected by PT2, resulting in assertion
of OVERPRESSURE. The OVERPRESSURE signal is routed to the PVM to release the
air pressure. The Main Board generates an alarm condition with the speaker
sounding and a message in the LCD.
Alaris Oral and Rectal TURBO TEMP Thermometry

The Monitor has one temperature channel for oral or rectal determinations.
When a temperature probe is attached to the temperature connector and to the
patient, TEMP input is routed to the DAS Board. This input represents the
temperature to be measured. The DAS Board converts the TEMP signal to a
digital signal and sends to Main Board. During the conversion, the Main Board
determines the patient temperature using either a predictive or monitor mode
algorithm depending on the user's setup. The patient temperature is distributed
as a digital signal to the LCD display or to the printer.
The Monitor has a probe check feature to determine if a probe is connected to
the Monitor and whether it is an oral or rectal probe.
ECG with Heart Rate and Respiration

The ECG parameter provides an electro-cardiographic waveform in 3-electrode
or 5-electrode configuration. The 3-electrode configuration derives a waveform
from Lead I, II, III and displays this waveform as the primary lead. The 5electrode configuration derives waveforms from Lead I, II, III, aVR, aVL, aVF, VA,
and displays this waveform as the primary lead. In 5-electrode configuration,
another waveform can be displayed as the secondary lead.
Breath rate is calculated by measuring the thoracic impedance between two
electrodes. As the patient breathes, the movement of the chest changes the
measured impedance to produce the respiration rate.
In the ECG menu for the monitor, the pacer detection option enables/disables
the pacemaker detection algorithm. It must be used whenever the monitored
patient has a pacemaker. Pace detection choices are PACE 1, PACE 2, and OFF.
DINAMAP
IS A TRADEMARK OF GE MEDICAL SYSTEMS INFORMATION TECHNOLOGIES.
Alaris Turbo Temp IS A TRADEMARK OF ALARIS MEDICAL SYSTEMS.
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Host Communication Port

An isolated host communication port provided on the back panel of the monitor.
The DB9 connector provides a channel of RS232 compatible communication.
NOTE: The DB9 connector should be used with approved interface devices
ONLY.
Communication Adaptor Connector

The nonisolated DB15 connector provides +5 V (500 mA Max), +12 V (250 mA
Max), Remote Alarm Signal, and two TTL communication channels. The
communication adaptor connector is used to interface the Monitor with other
electronic devices. (a central nurse's station or remote alarm device). Signals can
be sent to the monitor to initiate blood pressure determinations and other
functions. Patient data can also be retrieved through this port.
NOTES:
When the network module is connected, remote alarm is not available. The
alarms will response on CIC directly.
When using the remote alarm, the monitor alarm should be considered the
primary alarm source. The remote alarm is used for secondary
consideration only.
WARNING
Auxiliary equipment connected to the Dash 2500 Patient
Monitor will result in the formation of an electromedical
system, and thus must comply with the requirements of EN
60601-1-1/ IEC 60101-1. All Communication Adaptor
Connectors are NON-ISOLATED and should be connected to
equipment conforming to respective IEC or ISO standards (e.g.
IEC60950 for data processing equipment), configured to
comply with IEC 60101-1-1 ONLY.
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DB15 / DB9 Connector Pin Assignments

Pins are numbered from right to left, top to bottom.
DB9 Connector Pins
DB15 Connector Pins

Pin
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Function
Pin
Function
Ground
DCD
TX2_Inverted TTL Transmit Data
TX2_RS232
RX2_Inverted TTL Receive Data
RX2_RS232
Fused +5 volts
DTR
Fused +12 volts
GND
No connection
DSR
Ground
RTS
Remote Alarm (open collector, 75mA Max Sink)
CTS
No Connection
No Connection
10
No Connection
11
TX1 Inverted TTL Transmit Data
12
Port Enable Control <low=port 2>

(When in use, DB9 4 & 5 disabled)
13
RX1 Inverted TTL Receive Data
14
No connection
15
No connection

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Functional Description
The following section provides the functional interface relationship. The Monitor
contains a number of electrical and electro-mechanical assemblies. These
assemblies are:
PSU Module
DC2DC PWA
Main Board
UI PWAs
DAS PWA
SpO2 PWA
Interface PWA
CCFL inverter PWA
Pneumatic control device
Liquid Crystal Display (LCD) Assembly
Printer (optional)
TURBO TEMPerature (optional)
NiMH Battery
PSU Module
The PSU module is an AC Mains to DC converter. The module receives AC power
from the mains input connector. When AC INPUT is applied to the module, the
module AC/DC Converter changes the AC INPUT supply via rectifier circuit to a
high voltage DC. The DC power is then routed through a high frequency
switching converter and regulated to 12 VDC. This supply is connected to the
DC2DC PWA for further regulation.
DC2DC PWA
The PSU supplies regulated DC power to Monitor. The DC2DC PWA is designed to
operate from the output of the AC MAINS PSU module
(+12 VDC), or from an internal NiMH rechargeable battery (+8.4 VDC). The PSU
automatically selects the power source based on the following priority:
Valid AC MAINS input
Valid NiMH battery
The DC2DC PWA converts the selected power source into the following main
voltages:
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VRAW1 (7 V-12 V DC)
+5V
+12V
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The +12 V printer supply voltage and AUX +12 V are up converted from VRAW1
and maintained by a boost regulator to +12 V.
VBAT is the battery voltage protected by a 100 mA auto-reset fuse. It is also
used to power the fail-safe alarm circuits on the Main Board.
The DC2DC PWA contains firmware that reports the charge status of the battery
to the secondary processor on the Main Board. The secondary processor
charges the battery at the fastest rate allowable while keeping the Monitor
power consumption under 60 W.
The host communication port control circuitry selects whether Channel 2 is
routed to the Comms connector (DB-9) or the wireless connector (DB-15). If
Channel 2 is routed to the Comms connector, it is configured for RS-232 signals.
Channel 1 and Channel 2 on the wireless connector are only available as
inverted TTL.
Main Board
The Main Board is configured with Flash ROM, EEPROM, RAM, Primary Processor,
Secondary Processor, and NIBP. The Primary Processor operates from a 4.9152
MHz crystal stepped up to 49.152 MHz. The Primary Processor services and
controls the RAM, Flash ROM, EEPROM, the physiological interface modular
devices and display backlighting. The Secondary Processor monitors the power
supply circuit and signals within the NIBP circuits, controls the power-on/off
sequences, and performs watchdog tasks on it and the Primary Processor
monitors. The Secondary Processor monitors the power supply circuit and
controls the battery back up enable when no external sources are present and
shuts down the unit when the battery is exhausted. It enables the battery
charging circuit based on the battery charge status, unit power consumption,
and the availability of an external power source.
The Random Access Memory (RAM) is composed of a SRAM chip and two SDRAM
chips. The 512 Kbytes of battery-backed SRAM is provided to store trend data
and to provide space for working algorithms and is accessed on bits D[0:15] of
the data bus. The two 64-Mbit SDRAM chips are set up to form a 32-bit data bus
on bits D[31:0] that is used for running the program and working memory. This
gives 16 Mbytes of memory with an access time of less that 20 ns. The program
is loaded (including the boot code) from the 16-bit FLASH Read Only Memory
(ROM). The Electronically Erasable Programmable Read Only Memory (EEPROM)
is an 8-bit chip that is used to store the calibration and other "setting" variables
that have to be maintained in the event of a complete power failure.
If a hardware or software error causes a malfunction, its watchdog will provide
an internal and external RESET (L) signal. The FAILSAFE controller causes the
FAILSAFE (L) signal to go low. This signal passes to the Secondary Processor,
which disables the Primary Processor's power supplies, thus turning it off.
FAILSAFE (L) also passes to the control logic, which dumps the cuff pressure. The
system is left in a safe state but remains ON to enable the Secondary Alarm to
stay active. The Primary Processor monitors the activity of the secondary via its
handshaking communications. If the Secondary fails, the Primary can assert the
FAILSAFE line by overriding the FAILSAFE controller. The Secondary Alarm is a
hardwired alarm that will sound in the event of a FAILSAFE condition. Pressing
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the OFF-key can immediately reset this alarm although it times-out after about
10 minutes.
SpO2 PWA
The Monitor can be configured with either NELLCOR or MASIMO SET SpO2
hardware in config manager menu. When the Monitor is configured with
NELLCOR hardware, only NELLCOR config manager menu is available; when
the Monitor is configured with MASIMO SET hardware, MASIMO SET config
manager menu is available.
The SpO2 processor monitors the pulse oximetry signal. The processor takes the
signals and derives the oxygen saturation and heart rate data and converts
them into serial data. The serial data from the SpO2 processor is repacked by
DAS board and sent across an isolation barrier (opto couplers) and passed to the
Primary Processor via a dual-channel UART.
UI PWAs
The UI PWAs provide access to the basic functions of the Monitor. The buttons
that control each function are integrated to form a touch pad front panel. The
AC LED is continuously green when an external power source is present or
flashing green when the unit does not recognize the battery. The battery LED is
continuously yellow when the unit is running on battery and flashes yellow
when the battery is low.
DAS PWA
The DAS PWA is composed of ECG and MPDAS. Both ECG and MPDAS are
isolated to earth, and isolated from each other.
ECG accepts signals from a 3-electrode cable or a 5-electrode cable for
processing. The 3-electrode cable provides a single lead configuration with Lead
I, Lead II, or Lead III available. The 5-electrode cable provides a configuration
with Lead I, II, III, aVR, aVL, aVF, VA and displays this waveform as the primary
lead. In 5-electrode configuration, another waveform can be displayed as the
secondary lead.
A hybrid on the PWA provides lead-to-lead defibrillator protection. In addition, a
passive R/C network located on this PWA provides the first stage of high
frequency filtering for EMC and ESU interference rejection. Two electrodes are
selected for ECG measurement by a multiplexer (LS0, LS1 signal controlled) and
passed to a differential amplifier. A second multiplexor selects the third
electrode (the one not sent to the differential amplifier) and drives the signal with
an amplified and inverted version of the common mode voltage of the two
measuring electrodes. This feedback action cancels most of the common mode
signal applied to the differential amplifier. The output signal from the differential
amplifier is then routed to the bandpass filter and pacemaker detection circuit.
The ECG PWA uses the pacemaker detection circuit to prevent pacemaker
signals from interfering with heart rate measurements. The ECG signals are sent
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through a bandpass filter designed to pass pacemaker pulses in preference to
ECG signals. The filter output is applied to a comparator that asserts an output
signal when the input signal exceeds its positive or negative threshold. This
output signal is used by the controller to blank the ECG signal channel and alert
the host to the presence of a pacemaker pulse. The filtered ECG signal is routed
to the A/D converter for transfer to the Main Board.
The respiration circuit uses the ECG electrodes to measure respiration rate. This
is achieved by applying an excitation current (65.536kHz, well outside the
bandwidth of normal ECG signals) generated by a square wave switch onto two
selected electrodes. The measured voltage drop is filtered, the baseline
component removed, and amplified. The analog voltage representing the
impedance is routed to A/D converter for transfer to the Main Board.
The ECG provides isolated power to its circuitry using an isolation transformer. A
transformer driver drives the transformer primary at a frequency of about 350
KHz. The voltage of the transformer secondary is full-wave rectified using two
Schottky barrier diodes. The isolated voltage is filtered by capacitors and
regulated by a +5 V regulator. Isolated ground is obtained from the center tap of
the transformer. The data transferred from the A/D converter to the host is
isolated using opto couplers.
In the temperature parameter, the Alaris probe and the calibration resistor
chain are connected to an AD7738 24-bit serial DAC, which is read by the micro
controller. The micro controller computes the resistance for the probe (and
associated leads) and transmits the resistance value to the Primary Processor in
a serial data stream.
Pneumatic Control
The pneumatic functional block includes the control signal decode logic, the
valve driver circuitry, the pump driver circuitry, and a safety interlock circuit.
There are two transducers on board, PT1 and PT2. PT1 is used for main readings
while PT2 confirms readings and is used to derive overpressure signals. The
following signals are multiplexed into a 16-bit SAR A/D converter via a
multiplexor:
PT1A - the output of the measurement pressure sensor after

amplification and filtering by means of a passive 1 KHz low pass antialias filter
PT1B - the output of the measurement pressure sensor after

amplification and filtering by means of a passive 20 Hz low pass antialias filter
PT2 - the output of the confirmation/over-pressure sensor after

amplification
TH REF - the voltage that the amplified PT2 has to attain before the
safety circuit cuts in.
VBAT- 1/4 ratio of VBAT voltage
Valve Sense
The 16-bit value out of the ADC is available on the data bus at D[15:0].
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Control signals for the board are derived via four different sources: direct control
from outputs of the processor, controls signal derived from processor address
write commands (which are stored in an addressable latch), signals derived from
the watchdog timer, and signals generated by the overpressure functional
block. The four valve control signals and the pump control signal are derived
from the write address and stored in an addressable latch. Latch values are
cleared by application of system RESET. Each latch signal is individually gated in
a programmable logic device (XC9572) with the fail safe input signal (watchdog
timer) and the overpressure latch output to ensure pressure is removed from the
patient cuff should either overpressure or processor failure condition occur. A
cross-coupled latch for overpressure is formed with discrete logic included in the
programmable logic device. It is set by the occurrence of an overpressure
condition existing for a period greater than 500 milliseconds. When this
condition occurs, Filter_OVP-0 transitions low setting the latch. The latch output
state is indicated by the Latched-OVP signal. The latch can only be cleared by
the PNEURESET input.
LCD Assembly
The Monitor series uses a TFT active-matrix-color liquid display. The 10.4 inch
diagonal color display area contains 640 x 480 pixels and is backlit by coldcathode fluorescent lamps.
The LCD has the following specific characteristics. These are neither defects nor
malfunctions:
The ambient temperature may affect the display condition of the LCD.
Uneven brightness and/or small spots may be noticed depending on

different display patterns.
The LCD is driven from the Primary Processor via buffers (HCT244) on a
dedicated LCD driver port:
Signal
Name
Clk
Clock
Vsync
Vertical Sync
Hsync
Horizontal
Sync
R[0:3]
Red bits (0:3)
G[0:3]
Green bits (0:3)
B[0:3]
Blue bits (0:3)
The display module has a 31-way control signal connector and a 3-way
backlight driving connector.
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Printer (Optional)
The Monitor uses a thermal graphics printer. The printer requires a 5 V supply for
its logic circuitry and 12 V (nominal) for the motor. The power and data lines are
connected to the DC2DC Board by a 40 pin connector. The data lines are
connected to the SCC3 port on the Primary Processor.
The printer has a built-in sensor to monitor the printer paper level. When the
printer is out of paper, it sends a PAPER OUT signal to the Secondary Processor.
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Interface
Panel
TURBO
TEMP
BOARD

2042481-001
AC MAIN
FAN
SPEAKER
ECG
Analog Output
N I BP
Pneumatic
connector
SpO2
TURBO TEMP
PROBE
OPTICAL
SENSOR
TURBO
HOLDER
Buffer
/MUX
Front
Amp
SOUND
D/A
ECG
MCU
A/D
Isolation Barrier
MPDAS
MCU
ECG/Respiration
Pace
Detector
Amplifier
LP filter
Isolation Barrier
PSU Module
DC2DC Board
Regulated
+5V/+3.3V
Regulated
+12V
VRAW1 (7 V-12 V DC)
Host communication
port
Isolated
RS232
Comm adaptor port
Network Module
NI BP PUMP
AIR HOSE
Power/Data
Non-isolate
Dash2500 SYSTEM BLOCK DIAGRAM
Battery
Serial 2
Isolation Barrier
Ethernet
CHARGER /
FUEL GAUGE
PRINTER
(OPTIONAL)
Isolated
MPDAS
Power
Supplies
Isolated
ECG
Power
Supplies
DAS board
MPDAS
OEM SpO2 board
Temperature
Respiration
Modulator
Respiration
Demodulator
Driven
GENERATOR
H
y
b
r
i
d
PT1 PT2
UARTS
DC-DC
3.3V REGULATOR
5V REGULATOR
SECONDARY
PROCESSOR
PRIMARY
PROCESSOR
REAL TIME
CLOCK
EEPROM
SRAM
DRAM
FLASH ROM
BOOT ROM
Mainboard
SERIAL
INTERFACE
PORTS
NIBP signal
processing
MANIFOLD
NBP Valve1
3/5
NBP Valve2
2-16
LEADWIRE
ECG
ENCODER
UI_RIGHT
BOARD
CCFL
TFT LCD
UI_LEFT
BOARD
Button
button
System Block Diagram
Revision C
Revision C
Installation

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3-1
For your notes
3-2

2042481-001
Revision C
Installation: Connections
Connections
Rear Panel Connections
The back of the Monitor has all ports for equipment.
NOTE: When using the remote alarm, the Monitor should be considered the
primary alarm source. The remote alarm is used for secondary
consideration only.
Power Up
After making all connections, plug the power cord into an AC wall outlet.
You can turn on the Dash 2500 Monitor by pressing either the Power button or
the Trim Knob. If the Monitor is using battery power, it can be turned on only by
the Power button on the front of the unit.
On power-up, the Monitor performs the following steps in the order listed:
Revision C
At initial power up, the fail safe alarm sounds briefly.
All indicator lights switch on.
The screen momentarily displays the GE Medical Systems Information

Technologies logo.
The Monitor performs a self-test - the screen displays the model and
revision number of the Monitor - and a start-up tone sounds.
The main waveform screen appears.

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3-3
Installation: Set Up/Configure
Set Up/Configure
Setting up the Dash 2500 Monitor for the First Time
Unpacking and Preparation for Installation
Unpack and identify the contents of all shipping materials:
Rear View of Monitor

1.
Remove the Monitor.
2.
If an additional grounding point is provided, unpack the grounding cord and

connect the grounding cord to the Earth Connector in the backside of the
Monitor. Connect the other side of the grounding cord to the hospital
grounding point.
3.
Unpack the AC cord. Plug the AC cord into the AC Mains input at the back of
the Monitor.
4.
Plug the AC cord into a Hospital Grounded AC receptacle. A green LED

illuminates on the front of the Monitor indicating that an AC source is
available.
5.
Prior to usage, it is necessary to charge the Monitor for 12 hours. This

calibrates the battery circuitry with the charge status of the battery.
Set the Date and the Clock

The Monitor uses a Trim Knob to navigate through the menu systems. Turing the
Trim Knob moves the arrow cursor, and pressing the Trim Knob makes the
selection.
3-4
1.
Power on the Monitor using the Power button.
2.
Use the Trim Knob to select the no option when the Monitor prompts to
admit a new patient.
3.
Press or turn the Trim Knob to access the Main Menu.

2042481-001
Revision C
4.
Turn the Trim Knob to scroll down the menu. The arrow at the bottom of the
list indicates that the list continues on a second screen. Highlight the other
system settings option and press the Trim Knob.
5.
Turn the Trim Knob to scroll down the menu to highlight the Adjust date &
time option. Press the Trim Knob to continue.
6.
Turn the Trim Knob to scroll down and highlight the appropriate date and
time components to be changed if necessary (Month, Day, Year, Hour,
Minute, Second). Press the Trim Knob. The field is displayed in a box. Turn
the Trim Knob to the desired number and press the Trim Knob.
7.
After all of the settings are changed, use the Trim Knob to scroll down and
highlight the set new time and date option. Press the Trim Knob to save the
settings and continue.
8.
The message, CAUTION! This will delete all trends, and stored
waveforms. Are you sure you want to do this? displays. Highlight the yes
option and press the Trim Knob. A pop-up window displays the message,
Clearing all trends, and stored waveforms. to confirm that the function is
processing.
Configure
Refer to Appendix C to configure and set up the Dash 2500 Monitor for patient
use.
Mounting Options
Please contact your local dealer and GE Medical systems Information
Technologies for help.
Software Upgrade
Please contact your local GE service provider to upgrade the lastest version of
software.
CAUTION
The monitor indicates a MEMORY LOSS when upgrade the
software. It causes the monitor to revert to factory default
settings. All the user settings, system histories and patients
data will be lost.
Refer to the Dash 2500 Software Download Instruction (PN 2039601-001) for the
procedure of software downloading.
Network set up
Refer to Chpater F Connection for network installation configuration procedure.
Revision C

2042481-001
3-5

For your notes
3-6

2042481-001
Revision C
4-1
Maintenance

2042481-001
Revision C
For your notes
4-2

2042481-001
Revision C
Maintenance: Maintenance Schedule
Maintenance Schedule
Manufacturer Recommendations
To ensure the Monitor is always functional when required, qualified service
personnel should perform the following regular maintenance.
Visual Inspection: Perform a visual inspection upon receipt of the

equipment, every 24 months thereafter, and prior to servicing the unit.
Cleaning: Clean the unit upon receipt of the equipment, every 24 months
thereafter, and each time the unit is serviced.
Conditioning the Batteries: Condition the batteries once every month or as

needed.
Calibrating the NIBP Software: Calibrate the software upon receipt of the
equipment, every 24 months thereafter, and each time the unit is opened
for service.
Electrical Safety Tests: Perform safety tests upon receipt of the equipment,
every 24 month thereafter, and each time the unit is serviced.
Checkout Procedure: Perform the checkout upon receipt of the equipment,

every 24 months thereafter, and each time the unit is serviced.
Manufacturer Responsibility
CAUTION
Failure on the part of all responsible individuals, hospitals or
institutions, employing the use of this device, to implement the
recommended maintenance schedule may cause equipment
failure. The manufacturer does not, in any manner, assume the
responsibility for performing the recommended maintenance
schedule, unless an Equipment Maintenance Agreement exists.
The sole responsibility rests with the individuals, hospitals, or
institutions utilizing the device.
Visual Inspection
The Monitor and its components should be carefully inspected prior to
installation, once every 24 months thereafter and each time the equipment is
serviced.
Revision C
Carefully inspect the equipment for physical damage to the case, the
display screen, and the keypad. Do not use the Monitor if damage is
determined. Refer damaged equipment to qualified service personnel.
Inspect all external connections for loose connectors or frayed cables. Have
any damaged connectors or cables replaced by qualified service personnel.
Inspect the display face for marks, scratches, or other damage.
Safety labels and inscription on the device are clearly legible.

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4-3
Cleaning
Cleaning the Monitor
Monitor Exterior
The exterior surfaces of the Dash 2500 Monitors may be cleaned with a
dampened, lint-free cloth. Use one of the following approved solutions:
Mild soap (diluted)

Commercial diluted bleach solution or bleach wipe, such as Dispatch
Brand Hospital Disinfectant with Bleach Single-Piece Towels
Commercial diluted ammonia solution
Wipe off cleaning solutions with a clean, dry cloth
Never use the following cleaning agents:
Abrasive cleaners or solvents of any kind
Acetone
Ketone
Alcohol-based cleaning agents
Betadine
Quaternary ammonium disinfectants such as Virex, Sani-Wipes, AsceptiWipes, or products containing similar active ingredients to these should be
avoided.
Cleaning solutions containing wax
Never pour or spray water or any cleaning solution on the equipment or

permit fluids to run behind switches, into connectors, into the recorder, or
into any ventilation openings in the equipment.
Display
To clean the display screen, use a soft, clean cloth dampened with a glass
cleaner. Never spray the glass cleaner directly onto the display, and never use
alcohol or hospital disinfectants like Cidex or Betadine.
Failure to follow these cleaning recommendations may melt, distort, or dull the
finish of displays and cases; blur lettering on labels; embrittle cases and lead to
cracks and breakage; or cause equipment failures. Use of non-approved
cleaning agents is considered abuse and is not covered under warranty.
Cuff Cleaning and Disinfection

General
The cuff must be thoroughly cleaned with the specified detergent before reuse.
The additional use of household bleach as described below provides at least
intermediate-level disinfection.
4-4
Apply cuff hose plugs before cleaning.

The following cleansing procedure was repeated 20 times on DURA-CUF
Blood Pressure Cuffs and once on SOFT-CUF Blood Pressure Cuffs without
affecting the performance of the cuff.

2042481-001
Revision C
While this procedure is adequate for cleaning/disinfection, it may not

remove all stains.
Do not immerse hoses.
Do not immerse cuffs without prior application of cuff hose caps.
Materials
Enzymatic detergent such as ENZOL enzymatic detergent (US) or

Cidezyme enzymatic detergent (UK)
Distilled water
10% solution of household bleach (5.25% sodium hypochlorite) in distilled

water
Soft cloths and soft-bristled brushes
Spray bottles
Procedure
1.
Prepare the enzymatic detergent according to the manufacturer's

instructions and the 10% bleach solution, in separate spray bottles.
2.
Spray the detergent liberally on device. If the material is dried on, allow the
cuff to sit for 1 minute. For soil on the soft part of the closure or the cuff
itself, wipe the material off with a soft cloth. For persistent contamination on
the soft part of the closure, use a soft-bristled brush to loosen particles.
Rinse with copious amounts of distilled water. Repeat until no visible
contamination remains. For soil on the hook part of the closure, use a softbristled brush to remove the material, and rinse with copious amounts of
distilled water. Repeat until no visible contamination remains.
3.
Spray the 10% bleach solution on the affected area until the area is
saturated. Allow the cuff to sit for 5 minutes.
4.
Wipe away any excess solution and rinse the cuff again with distilled water.
Allow 2 hours for drying.
The user has the responsibility to validate any deviations from the
recommended method of cleaning and disinfection.
For additional information on infection control procedures, contact GE Medical
Systems Information Technologies Technical Support.
Temperature Devices
Do not immerse predictive temperature probes. The probe can be cleaned with a
solution of 10% bleach in water. Use a cloth or sponge-just damp, not wet-and
avoid getting any liquid into the interior of the probe.
SpO2 Sensors
Adhesive sensors are sterile and for single use only. Reusable sensors should be
cleaned before reuse with a 70% alcohol solution. If low-level disinfection is
required, use a 1:10 bleach solution. Do not use undiluted bleach (5% - 5.25%
sodium chlorite) or any cleaning solution other than those recommended here
because permanent damage to the sensor could occur. Do not sterilize the
Revision C

2042481-001
4-5
Maintenance: Periodic Maintenance

sensor by irradiation, steam, or ethylene oxide. If disposable sensors or their
packaging are damaged, they must be disposed of as advised in this section.
To clean or disinfect the sensor:

1.
Saturate a clean, dry gauze pad with the cleaning solution. Wipe all surfaces
of the sensor and cable with this gauze pad.
2.
Saturate another clean, dry gauze pad with sterile or distilled water. Wipe all
surfaces of the sensor and cable with this gauze pad.
3.
Dry the sensor and cable by wiping all surfaces with a clean, dry gauze pad.
Periodic Maintenance
Integrity of Hoses and Cuffs
When the pneumatic integrity of any NIBP cuff or hose is in doubt, replace the
cuff and hose, and discard the questionable accessories.
Long-Term Storage
If it becomes necessary to store the Monitor for an extended period of time,
remove all attached accessories. Attach the original packing inserts, and place
the Monitor into the original shipping container.
Generally, long-term storage of a nickel-metal hydride battery in either a
charged or discharged condition has no permanent effect on capacity. Capacity
loss due to self-discharge is reversible, and nickel-metal hydride batteries can
recover to full capacity by proper recharging. For example, cycling through
repeated charge/discharge cycles can restore a full capacity of a nickel-metal
hydride battery that was stored at room temperature for up to one year.
Long-term storage at high temperatures can lead to deterioration of seals and
separators and should be avoided.
Periodic Procedures
Perform the test procedures described in every 24 months, or whenever the
accuracy is in doubt.
NOTE:
An internal, 3.6 V NiMH battery acts as an alarm backup and maintains the
nonvolatile RAM memory when the Monitor is off or away from AC mains. A
system alarm message is generated if backup battery replacement is
required.
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2042481-001
Revision C
Maintenance: Periodic Maintenance
Care of Storage Batteries

The Monitor uses one nickel-metal-hydride (NiMH) storage battery. The battery
can be charged at any time without reducing the charging capacity. Take out
the battery pack if storing for long term; over discharge might impair the
battery.
Procedures For First Use

Follow these procedures to condition a new NiMH battery and optimize its
performance:
The internal battery automatically charges when the AC power supply is in use.
NOTE:
When the battery is charged for the first time, the charger may indicate
prematurely that charging is complete. This is normal and can happen with
all rechargeable batteries when first charged.
Battery Charging
The Monitor charges the NiMH battery whenever the AC power supply is in use.
The Monitor automatically senses if the battery needs recharging. Battery
charging continues whenever it's needed while the Monitor is connected to the
AC power supply, even when the Monitor is turned off.
Batteries should be charged before first use or after prolonged periods of

storage for at least 12 hours.
The battery should be charged at room temperature (59F - 86F; 16C 30C).
It is normal for the battery to become warm during charging or after use.
Batteries can be charged or topped-off at any time. It is not necessary to

wait until they are fully discharged.
If the Monitor is idle for extended periods, it should be at least fully charged
and discharged once a month to ensure optimum performance.
Battery Maintenance
Battery should be maintained to prolong its life. Do not monitor patients during
maintenance. Maintenance procedures are as follows:
Revision C
Connect the power cord to the Monitor and the AC wall outlet.
Power the Monitor on and verify the battery is charging.
Power the Monitor off and leave attached to AC power for a minimum of 4
hours (8 hours recommended).
Power the Monitor on and verify the battery charge status. If further
charging is required, power the Monitor off and recheck every 30 minutes
(or longer) until the battery is fully charged.
If the required charge time exceeds 12 hours, replace the battery.

2042481-001
4-7
Maintenance:
Battery Troubleshooting
Trouble
Problem Cause
Remedy
Battery inoperative
or does not last
very long.
Battery not fully charged.

Battery in long-term
storage or non-use.
Charge and discharge battery up to

three times for optimum performance.
Battery will not

charge.
Charging battery in
unusually cold or hot
temperatures.
Charge at basic room temperature of

59F (16C) to 86F (30C). Slowly bring
battery to basic room temperature
before recharging. Batteries cannot be
fully charged unless internal
temperatures between 57F (15C) and
109F (40C).
Electrical Safety Tests

General
Electrical safety tests provide a method of determining if potential electrical
health hazards to the patient or operator of the device exist.
These instructions are intended for every component in the system.
Test Equipment
The recommended test equipment required to perform electrical safety tests is
listed below.
Item
Specification
Leakage Current Tester
Equivalent to the circuits shown
ECG Test Body
All leads together
Masimo SET SPO2 Test Body
2006036-001
Safety Resistance Testing

Using a safety analyzer (Dynatech Nevada Model 235A or equivalent), check the
ground resistance of the Monitor. Refer to the Rear View of Monitor with Safety
Connection Exposed graphic for locations of test points.
4-8

2042481-001
Revision C
Maintenance: Electrical Safety Tests
Rear View of Monitor with Safety Connection Exposed

Earth-To-Secondary Continuity Verify that the resistance between the AC
mains ground pin and the earth ground is less than 0.1 .
AC Mains Leakage - Normal Polarity 260 VAC is applied at the Monitor's AC
Mains input in normal polarity.
No Fault Verify that the leakage from line to ground pin is less than 500 A.
Open Ground Disconnect the Monitor's ground lead from earth ground (for the
duration of this test only) and verify that the leakage from line to ground pin is
less than 500 A.
Open Neutral Open the Monitor's neutral lead (for this test only) and verify
that the leakage from line to ground is less 500 A.
AC Mains Leakage - Reverse Polarity 260 VAC is applied at the Monitor's AC
Mains input in reverse polarity (inputs to line pin and Neutral pin reversed).
No Fault Verify that the leakage from line to ground pole is less than 500 A.
Open Ground Disconnect the Monitor's ground lead from earth ground (for the
duration of this test only) and verify that the leakage from line to ground is less
than 500 A.
Open Neutral Open the Monitor's Neutral lead (for the duration of this test
only) and verify that the leakage from line to the ground is less than 500 A.
Revision C

2042481-001
4-9
Patient (Source) Leakage Current Test

This procedure measures the leakage current from the ECG/RESP connector or
the SPO2 connector or the TurboTemp of the device to ground..
Patient (Source) Leakage From ECG/Resp connector to Ground

Normal Polarity - Configure the leakage tester like the circuit shown above with
GND switch CLOSE and polarity switch NORM.
No Fault - Verify that the leakage current from ECG test body to ground pin is
less than 10 A (0.01 volts on the DMM).
Open Ground - Change the GND switch to the Open position. Verify that the
leakage current from ECG test body to ground pin is less than 50 A (0.05 volts
on the DMM).
Reverse Polarity - Change the leakage current switch to the RVS position with
GND switch CLOSE.
No Fault - Verify that the leakage current from ECG test body to ground pin is
leakage current from ECG test body to ground pin is less than 50 A (0.05 volts
on the DMM).
Patient (Source) Leakage From SpO2 connector to Ground
GND switch CLOSE and polarity switch NORM. Connect the SpO2 Test Body to
the blue SpO2 connector of the device under test, using the appropriate SpO2
Test Body.
No Fault - Verify that the leakage current from SpO2 test body to ground pin is
4-10

2042481-001
Revision C

leakage current from SpO2 test body to ground pin is less than 500 A (0.5 volts
on the DMM).
GND switch CLOSE.
No Fault - Verify that the leakage current from SpO2 test body to ground pin is
leakage current from SpO2 test body to ground pin is less than 500 A (0.5 volts
on the DMM).
Patient (Source) Leakage From TurboTemp connector to Ground
GND switch CLOSE and polarity switch NORM. Connect the Probe to the
TurboTemp connector of the device under test.
No Fault - Verify that the leakage current from TurboTemp Probe to ground pin
is less than 100 A (0.1 volts on the DMM).
leakage current from TurboTemp Probe to ground pin is less than 500 A (0.5
volts on the DMM).
GND switch CLOSE.
No Fault - Verify that the leakage current from TurboTemp Probe to ground pin
is less than 100 A (0.1 volts on the DMM).
leakage current from TurboTemp Probe to ground pin is less than 500 A (0.5
volts on the DMM).
Revision C

2042481-001
4-11
Patient (Sink) Leakage Current Testing (Mains Voltage on the Applied Part)
This procedure measures the leakage current from a mains voltage source
into the ECG/RESP connector or the SpO2 connector or the TurboTemp
connector of the device. .
Patient (Sink) Leakage From AC mains to ECG/Resp connector

GND switch CLOSE and polarity switch NORM. Verify that the leakage current
from ECG test body to ground pin is less than 50 A (0.05 volts on the DMM).
GND switch CLOSE.Verify that the leakage current from ECG test body to ground
pin is less than 50 A (0.05 volts on the DMM).
Patient (Sink) Leakage From AC mains to SpO2 connector
GND switch CLOSE and polarity switch NORM. Connect the SpO2 Test Body to
the blue SPO2 connector of the device under test, using the appropriate SpO2
Test Body.
Verify that the leakage current from SpO2 test body to ground pin is less than
5mA (5 volts on the DMM).
GND switch CLOSE.
Verify that the leakage current from SpO2 test body to ground pin is less than
Patient (Sink) Leakage From AC mains to TurboTemp connector
GND switch CLOSE and polarity switch NORM. Connect the Probe to the
TurboTemp connector of the device under test.
Verify that the leakage current from TurboTemp Probe to ground pin is less than
4-12

2042481-001
Revision C
Maintenance: Checkout Procedures

GND switch CLOSE.
Verify that the leakage current from TurboTemp Probe to ground pin is less than
Checkout Procedures
These checkout procedures provide service personnel with a method to verify
operational and functional performance of the Monitor. Failure to attain any of
the listed results indicates a potential malfunction of the Monitor.
Perform the checkout procedures when you receive the Monitor, every 24
months thereafter, and each time you service the unit.
The checkout procedures are based on the assumption that the tested monitor
has known good cables and test equipment. It also requires that the user be
familiar with the operation of all test equipment required for the checkout
procedures. For more information concerning the operation of these
components, refer to the operation manual.
NOTE: All devices are tested and calibrated during manufacturing and are
certified for operation at installation.
Parameter Level Functional Testing

After the initial configuration is complete, perform functional testing of each of
the parameters. Using the accessories supplied with the Monitor, initialize the
Monitor in such a way that only one parameter is functioning at a time.
Left Side View of Monitor
Revision C

2042481-001
4-13
Right Side View of Monitor
Functional tests to be performed:
SpO2: The SpO2 sensor used depends on the Monitor configuration.

NELLCOR SpO2 configured monitors use an assembly consisting of two
parts: the DS-100A, and the extender cable NELL1 GE cable.
MASIMO SET SpO2 configured monitors use an assembly consisting of
an interface cable and a sensor.
Connect the cables prior to attaching to the Monitor. An SpO2 reading
displays within moments of attaching the sensor to either an SpO2
simulator or to your finger.
Blood Pressure: A blood pressure test is carried out by connecting the

supplied hose and cuff together, then attaching them to the NIBP Connector
on the left side of the Monitor. Press the NIBP Go/Stop hardkey on the front
to begin the NIBP cycle.
ECG: ECG monitoring uses 3-electrode or 5-electrode configuration.

3-Lead ECG connection Connect the ECG lead connector to the ECG trunk
cable prior to connecting to the Monitor. The simplest way to function test
the ECG circuits is through the usage of an ECG simulator.
5-Lead ECG connection Connect the ECG lead connector to the ECG trunk
cable prior to connecting to the Monitor. The simplest way to function test
the ECG circuits is through the usage of an ECG simulator.
Temperature: Connect the supplied temperature probe to the

corresponding connection. A predictive temperature begins once the probe
is removed from the holster. Replace the probe after completion of the TEMP
cycle.
Service Mode Operation

The Monitor Service Mode exercises the built-in diagnostic features of the
Monitor and the installed parameters. Access the Service Mode from a cold start
by proceeding as follows:
4-14

2042481-001
Revision C

1.
Power on the Monitor using the Power hardkey.
2.
Use the Trim Knob to select the no option when the Monitor prompts to
admit a new patient.
3.
Press or turn the Trim Knob to access the Main Menu.
4.
Turn the Trim Knob to scroll down the menu. The arrow at the bottom of the
list indicates that the list continues on a second screen. Highlight the other
system settings option and press the Trim Knob.
5.
Highlight the go to service mode option and press the Trim Knob. Turn the
Trim Knob and press the Trim Knob again to answer yes at the prompt to
display the dialog box.
6.
A row of numbers is displayed at the bottom of the screen. Turn the Trim
Knob and move the arrow to the desired number, then press the Trim Knob
to select the number. Enter the Service Mode password, 2213.
7.
After the password is selected, turn the Trim Knob to the DONE option and
press the Trim Knob.
8.
In the process of entering the Service Mode, the Monitor resets itself.
Successful entry into the Service Mode is indicated by the Service Menu title
displayed on the upper left side of the display.
NOTE:
The Service Mode can also be entered directly from a cold start by
pressing and holding the following two keys until full power-up: Power
and NIBP Auto. To make any changes to the Service Menu, the
password has to be entered, follow Step 6.
9.
Revision C
At this point the Service Mode main screen should be present in the main
display, as shown in the following graphic. The Service Menu service
parameters area displays a list that corresponds to the number and type of
parameters that have been detected by the Monitor. If the Service Mode
was entered directly (as described in the NOTE above), enter service
password appears above the service parameters on the Service Menu. The
password MUST be entered (as described in Steps 5 and 6) before any
changes to calibration can be made.

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4-15
Main Service Menu

For each parameter, there are one or more service screens that display
operating values and tests that are applicable to the parameter type. Refer to
the following paragraphs for information about each parameter. At the
conclusion of the tests, select go to service menu at the top of the screen to
return to the Service Menu main screen.
NOTE:
Additional resources depend on the configuration of the Monitor.
SpO2 Testing
For Monitors With NELLCOR SpO2 NELLCOR recommends use of the SRCMAX Portable Tester for use with the Dash 2500 Monitor equipped with the
NELLCOR SpO2 system.
On occasion when testing the integrity of the NELLCOR oximetry system,
abnormal results may occur when introducing large changes in the pulse rate
and/or pulse amplitude. Extreme changes in the rate sent to the NELLCOR
sensor by the SpO2 simulator may cause the SpO2 algorithm to completely miss
finding the pulse rate. This is an expected result. To work around this,
incrementally step up or down the settings on your SpO2 simulator and allow
the Monitor to detect and display the new pulse rate or saturation.
For Monitors With MASIMO SET SpO2MASIMO SET recommends BIO-TEK
SpO2 simulators.
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2042481-001
Revision C
Test Procedure
The following table shows the allowable tolerance of the indicated simulator
values.
Range
Accuracy
70% - 100% (Adult/

Ped)
2 digits
70% - 100% (Neonate)
3 digits
1% - 69%
No accuracy
required
The following procedure applies to both Nellcor and Masimo equipped units.
1.
Disconnect all sensor cables from the SpO2 Parameter, and ensure that the
SpO2 parameter is listed within the main Service Menu.
2.
From the Service Menu, turn and press the Trim Knob to select the SpO2
service parameter. The SpO2 service menu appears. The text under Error
and Version sections reflects the installed type of SpO2. The illustration
shows both text examples.
SpO2 Service Menu
Revision C
3.
All SpO2 mode operations take place with MASIMO SET and NELLCOR
power-up defaults. No menu settings are reflected.
4.
Connect the appropriate SpO2 simulator and cable to the SpO2 parameter.
Be sure it is fully seated in the socket.

2042481-001
4-17

5.
Vary the values on the simulator. Verify that the Monitor responds
accordingly by displaying the proper heart rate value and saturation value.
NIBP Testing
NIBP Service Menu

Perform the following tests to determine that the NIBP parameter is functioning
normally.
Always enter Service Mode with the password before attempting to recalibrate
equipment.
CAUTION
Calibration equipment should always be kept dry and free of
particulate matter. Moisture or foreign substances introduced
to the pneumatic system will likely cause damage to the
Monitor and/or accessories.
4-18

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Revision C
NIBP Leak Test

1.
Using the calibration kit, an adult cuff and air hose, and a manometer, set up
the equipment as shown in the NIBP Test Setup graphic. Connect the hose
to the NIBP Parameter. Make sure that all of the fittings are tight and that
the valve on the manual inflation bulb is fully closed.
NIBP Test Setup
Revision C
2.
From the Service Menu, turn and press the Trim Knob to select the NIBP
service parameter.
3.
Turn and press the Trim Knob to select start leak test. Observe that the
Leak Test Status message on the menu indicates Busy.
4.
Observe that the pump begins inflating the system to 200 - 210 mmHg, at
which point the pump operation will cease. The Monitor will begin to
calculate system pressure loss rate.
5.
After about 60 seconds the pressure is released, and the menu should
display Leak Test Status Passed, and the Leak Test Results indication
should be a value less than 6. Service Error: None should continue to
display.
6.
If the menu displays Leak Test Failed, continue with Steps 7 through 9.

2042481-001
4-19

7.
the equipment as shown in the Leak Test Setup graphic.
Leak Test Setup

8.
Close the pressure release valve on the manometer inflation bulb and slowly
increase the pressure to 200 mmHg 1 mmHg.
9.
Verify the pressure indicated on the manometer remains within 5 mmHg of

200 mmHg for 60 seconds. If not, either the cuff or hose or both may be
defective. If the cuff and hose pass this test, repeat Steps 1 through 7 to try
to isolate the leak. Repeat the leak test for all cuff and hose combinations to
be used with the Monitor.
NIBP Calibration Check
4-20
1.
to the NIBP Parameter. Make sure all fittings are tight and that the inflation
bulb valve is closed tightly.
2.
From the Service Menu, turn and press the Trim Knob to select the NIBP
service parameter.
3.
Turn and press the Trim Knob to select pneumatic reset.
4.
Turn and press the Trim Knob to select valve close.
5.
Observe that both PT1 Pressure and PT2 Pressure equal initial values of 0
mmHg.
6.
Connect the pneumatic hose to the Monitor's NIBP port.
7.
Fold the adult cuff so the index line is aligned with the inner range mark on
the inside of the cuff. Make sure all fittings are tight and that the valve on the
inflation bulb is closed tightly. If there is doubt about the integrity of the
system, perform the leak test before continuing.
8.
Close the pressure release valve on the manometer inflation bulb and
manually pump up the pressure until the manometer indicates
approximately 220 mmHg.

2042481-001
Revision C

9.
Allow the pressure to stabilize for at least 1 minute. Then open the pressure
release valve on the manometer inflation bulb and carefully bleed off
pressure until the manometer indicates 200 mmHg.
10. Observe that the values of PT1 Pressure and PT2 Pressure on the menu
indicate within 1 mmHg of the pressure shown on the manometer. If not,
please check and repair the device.
11. Verify the system linearity by repeating Steps 8 and 9 using manometer
readings of 250 mmHg, 150 mmHg, and 50 mmHg. Observe that the PT1
and PT2 Pressures are within 3 mmHg of manometer readings for each of
these pressure indications. If not, proceed to the Pressure Recalibration
section.
Pressure Recalibration
1.
the equipment as shown in the NIBP Test Setup graphic. Do not connect the
pneumatic hose to the NIBP port yet.
2.
From the Service Menu, Turn and press the Trim Knob to select the NIBP
service parameter.
3.
4.
5.
Observe that both PT1 Pressure and PT2 Pressure display initial values of 0
on the menu.
6.
Turn and press the Trim Knob to select cal press zero. Observe that the
message Inflate System to 200 mmHg Then Hit Cal Press 200 is displayed
on menu.
7.
Connect hose to NIBP Parameter.
8.
Fold the adult cuff so the index line is aligned with the inner range mark on
the inside of the cuff. Make sure all fittings are tight and that the valve on the
inflation bulb is closed tightly. If there is doubt about the integrity of the
system, perform the leak test before continuing.
9.
Close the pressure release valve on the manometer inflation bulb and
manually pump up the pressure until the manometer indicates
approximately 220 mmHg.
10. Allow the pressure to stabilize for at least 1 minute. Then open the pressure
release valve on the manometer inflation bulb and carefully bleed off
pressure until the manometer indicates a little more than 200 mmHg.
11. Turn and press the Trim Knob to select cal press 200, but do not press the
Trim Knob.
12. When the manometer indicates exactly 200 mmHg, press the Trim Knob.
Observe that system pressure is released, and the message, !!!!! CAL INFO
NOT SAVED!!!!! Service Error: None is displayed on menu.
13. Turn and press the Trim Knob to select save cal info. The message, !!!!!CAL
INFO NOT SAVED!!!! disappears. This indicates your new calibration values
have been saved.
14. Repeat the calibration check procedure to confirm the calibration setting.
Revision C

2042481-001
4-21
Overpressure Tests
1.
to the NIBP Parameter. Make sure all fittings are tight and that valve on
inflation bulb is closed tightly.
2.
From the Service Menu, Turn and press the Trim Knob to select the NIBP
service parameter.
3.
4.
5.
Verify the menu displays Overpressure Latch: Cleared and Overpressure

Selected: Adult. If not, turn and press the Trim Knob to select adult ovp
select.
6.
Turn and press the Trim Knob to select inflate on. The pump should begin to
inflate the system.
7.
Watch the pressure indication increase on the manometer, and observe

that the pump is shut down and the pressure is released when the
manometer indicates in the range of 300 to 330 mmHg. Observe that the
menu displays Service Error: Over Pressure Condition Detected.
8.
9.
10. Turn and press the Trim Knob to select neo ovp select. Verify the menu
displays Overpressure Latch: Cleared and Overpressure Selected: Neo.
11. Turn and press the Trim Knob to select inflate on. The pump should begin to
inflate the system.
12. Watch the pressure indication increase on the manometer, and observe
that the pump is shut down and the pressure is released when the
manometer indicates in the range of 150 to 165 mmHg. Observe that the
menu displays Service Error: Over Pressure Condition Detected.
13. If the overpressure test results in an out of tolerance condition, contact GE
Medical Systems Information Technologies Technical Support at 1-800-5587044 (USA), 86-800-810-8188 (China) or contact your local representative. If
you are a cell phone or Xiaolingtong user, or your area does not support 800
free-call service, please dial: 86-010-67882652 (China). If you are a EMEA
user, please contact your local GE service provider.
Overpressure Calibration
NOTE:
Overpressure calibration is adjusted by software based on Pressure
Calibration section.
4-22

2042481-001
Revision C
ECG Testing
Connect the ECG leads to the ECG trunk cable prior to connection to the Monitor.
The simplest way to function test the ECG circuitry is through the usage of an
ECG simulator with the Monitor in normal monitoring mode.
1.
Set the ECG simulator to output a Paced ECG Waveform.
2.
Press Power hardkey to power up UUT.
3.
Select no at new patient prompt. Set the ECG high alarm to 150 and the low
alarm to 50.
4.
Verify that the ECG waveform is displayed on LCD display.
5.
From ECG menu, select Pace 1 and verify paced marker on display
waveform.
6.
From ECG menu, select Pace 2 and verify paced marker on display
waveform.
7.
From ECG menu, select PACE OFF. Turn paced off on simulator.
8.
After unit has learned the patient waveform change the bpm to 30.
9.
Verify HR LOW alarm and HR is 30 + 4 bpm on unit.
10. Set ECG simulator to 160 bpm.

11. Verify that the ECG waveform is displayed on the LCD display.
12. Verify HR HIGH alarm and HR is 160 4 bpm on unit.
14. Set ECG high alarm to 200 and low alarm to 30.
15. Set ECG simulator to VTACH.
Set simulator MPS450 to 160 bpm
Set simulator MPS214B to 180 bpm
16. Verify ECG VTACH alarm and HR is 180 4 bpm.

Revision C

2042481-001
4-23

18. Press Silence Alarm hardkey to acknowledge the alarm and verify HR is 80
+4.
19. Connect scope to analog output using 1/8" stereo plug (+ to ring, - to shield).
20. Verify that the ECG waveform is displayed on the scope (amplitude
approximately 1V/mV).
21. Disconnect scope from analog output.
22. Remove and reattach Leads I, II, III, sequentially and verify ECG LEAD FAIL
alarm on display.
23. From ECG menu, select turn parameter off.
RESP Testing
1.
Set simulator Respiration to 20 BrPM.
2.
Set simulator delta ohms to 1.0.
3.
Set simulator Baseline to 1K, and Lead to II.
4.
Verify that the RESP waveform is displayed on the LCD display.
5.
Record and verify the UUT RESP reading 20 + 3bpm.
6.
Set simulator Respiration to 60 BrPM.
7.
Record and verify the UUT RESP reading 60 + 3bpm.
8.
From RESP menu, select turn parameter off.
Temperature (Perform if equipped with Temp module)

The Temperature Simulator for the Alaris System is available from Alaris Medical
Systems, Inc. (619) 458-7000.
The Alaris Turbo Temp probes cannot be calibrated. These probes must be
discarded after 2 years from the date of manufacture stamped into the RJ45
connector (first two digits = year, second two digits = week). Refer to the
illustration example (0520 = fw20 in 2005).
It is the responsibility of the user to maintain proper records.
4-24

2042481-001
Revision C

Alaris Turbo Temp Probe Date Code
1.
Turn Monitor off. Make sure the temp probe is properly stored in the probe
well.
2.
Disconnect the temp probe cable from the monitor.
3.
Connect Temp simulator; set to 80.2F.
4.
Turn the Monitor on.
5.
Put the Monitor into temp monitor mode:

a.
partially remove the probe from the well (stop when you hear the
Monitor beep).
b.
Quickly re-insert the probe and remove again (you should hear two
beeps of a different tone).
c.
A temperature value should appear quickly, if not, repeat Step 5b.
6.
Record and verify the reading in the temp display is 80.2 0.2F.
7.
Set the simulator to 98.6F.
8.
Record and verify the reading in the temp display is 98.6 0.2F.
9.
Set the simulator to 107.8F.
10. Record and verify the reading in the temp display is 107.8 0.2F.
11. Calibration is complete. If the monitor does no pass the calibration
verification then contact Technical Support.
Recorder Testing (if installed)
Revision C
1.
Ensure that paper has been loaded into the Recorder and you are presently
in the Service Mode.
2.
From the Service Menu, turn and press the Trim Knob to select the Recorder
test option. Turn and press the Trim Knob to select the Print 1 Waveforms

2042481-001
4-25

option. Turn and press the Trim Knob to select the Wave Test 6.25 mm/s
option. Verify that all printouts are of even tone and all pixels are present.
Sample 6.25 mm/s - 1 waveform chosen

3.
Allow for the paper to spool out a 12-inch printed section then press Stop
Test.
4.
Select Vertical Text test. Verify that the printed text is legible and evenly
spaced.
Vertical Text Test Printout

5.
Select Horizontal Text test. Verify that the printed text is legible and evenly
spaced.
Horizontal Text Test Printout
4-26

2042481-001
Revision C
Battery Testing
From within the Service Menu, battery status information is displayed on the
upper right-hand section of the display.
Battery/ Power Supply Menu
Battery Health
The Monitor's software approximates the true status of the battery's health. The
value indicated is displayed as both a number (in percentage) on the top of the
display and as an icon on the lower right area of the display.
External Supply available

TRUE indicates a source other than the internal battery is providing power for
the Monitor and a source to charge the internal battery.
External Supply Sufficient to Charge

If the voltage from the external supply is greater than that of the internal
battery, the Monitor will display the results as TRUE. FALSE will result if either the
voltage is equal to or lower than the power available from the internal battery.
Charge Type
FAST indicates battery is charged fast when it is not full. TRICLE indicates
battery is charged slowly when it is already full.
Battery Failed
Any result other than FALSE indicates that the internal battery has suffered a
failure and should be investigated.
Revision C

2042481-001
4-27
Charger Supply Enabled

This status indicator should always be TRUE as the Monitor consistently
attempts to keep the battery at its fullest capacity. A FALSE indicates the battery
may be faulty, not installed, or the charge circuit may have failed. Also, if no
external source of power is available, the Monitor registers a FALSE result.
Test Procedure
1.
Verify AC Mains indicator on front panel of unit near Power hardkey is lit
with AC Mains plugged in.
2.
Turn on Monitor.
3.
Remove AC Mains and verify uninterrupted battery operation.

NOTE:
If this fails, check fuse in communications well.
4.
Verify battery indicator near Power hardkey.

NOTE:
Battery life is dependent upon battery usage. A fully charged battery
should last greater than 180 minutes using the following setup: (NIBP: 5min auto cycle with adult cuff. ECG, RESP, SpO2: Active. TEMP: predictive
mode. Printer: printing 2 waveforms for 1 min every 20 min at 25 mm/
s.).
Fail-Safe Logic Testing

From the Service Menu, turn the Trim Knob to select test fail-safe logic. A
dialogue box displays: CAUTION! This causes the system to freeze for approx.
2 seconds then enter the fail-safe mode. Continue?
1.
Turn the Trim Knob to the yes option and press the Trim Knob.
2.
After 2 seconds, the system freezes, an alarm sounds, and the screen goes
blank. Recycle the system power using the Power hardkey. To return to the
Service Mode, repeat the procedures as described in Service Mode section.
1.
From the Service Menu, turn and press the Trim Knob to select keypad KEY
test. With the exception of the Power hardkey, verify that each key press
produces a tone. You may hear different tones in some occasions. This does
not affect the testing results.
2.
After all keys have been tested, press the Trim Knob again to stop the test.
1.
From the Service Menu, turn and press the Trim Knob to select Sound Test.
2.
Select ON to start the test. The monitor generates a serial of tones the
Monitor has one by one every 2 seconds.
3.
Select OFF to stop the test.
Keypad Key Testing
Sound Testing
4-28

2042481-001
Revision C
Communications Testing
Set up Terminal
1.
Connect serial communication cable from PC to rear of UUT (DB9).
2.
Invoke terminal program with settings:

9600 baud,
No parity,
8 bits,
1 stop bit,
flow = None,
no cr/lf character enabled
NOTE:
Terminal must be set to an available communication port (comm1 is
default) or redirect the terminal program to an appropriate port.
Configure UUT for Communication

1.
Turn the Trim Knob to get to the Main Menu and select other system
settings.
2.
Select go to config mode, select yes at the verification prompt.
3.
Enter password 2508, and select done.
4.
After the unit reboots, turn the Trim Knob to display the Configuration
Menu.
5.
Select other system settings, then Config HostComm.
6.
Configure the COMMS port for Remote access Serial 2.
7.
Select Serial 2 setup and configure Serial 2 for ASCII cmd, 9600 baud.
8.
Select go to previous menu, then save default changes.
9.
Select exit config mode, select yes at the verification prompt.
10. After the unit reboots, select no at "new patient" prompt.
Communication Test
Execute the following commands (by sending text files from the terminal
program) and verify the appropriate response.
NOTE:
Each string is preceded by a space. "^" represents the space character.
"^NC0!E" Verify that UUT pump starts.
"^ND!5" Verify that UUT pump stops.
"^TB!9" Verify return temperature status in the form "...TB-99999...".
Revision C

2042481-001
4-29
Remote Alarm Testing

1.
Install the test plug into 15 pin communications port on rear of unit, as
shown in Test Plug Assembly graphic.
2.
Use the DMM to measure voltage between pins 4 and 8 of DB15 connector
and record the result.
REMOTE ALARM TEST PLUG
15
1
14
2
13
3
12
4
11
5
10
6
9
7
470
15 PIN MALE (FRONT VIEW)
Test Plug Assembly

3.
From the Service Menu, turn and press the Trim Knob to select Alarm relay.
4.
Select Alarm relay / ON. Measure and record voltage between pins 4 and 8
of DB15 connector. Verify the voltage is 0 V.
5.
Select Alarm relay / OFF. Measure and record voltage between pins 4 and 8
of DB15 connector. Verify the voltage is 5 V.
6.
Remove test plug assembly from DMM.
Network Testing
Install and set up the network module for Dash 2500. Check that the connector
and the plugs are clean and intact, then connect the monitor into the network.
Select View patient tab on the CIC, set up the unit number and bed number of
the connected monitor to establish communication. If the unit name is the same
as CIC unit setting on the monitor, the CIC will establish communication
automatically. If it does not display automatically, right click an multi-patient
view window and select the correct unit/bed of the monitor.
NOTE: In general, it needs less than 30 seconds to let monitor to be detected
and establish communication by CIC after you finished all above steps.
If the monitor information (e.g. bed number, unit number, and patient name) is
displayed on the CIC patient tab, the communication is established successfully.
Country of Use
This option have two setting values: CHINA and Other. The CHINA setting will
cause the monitor to have the same factory default, ECG parameter, QRS width
setting between adult, pediatric, and neonate patient types. The user can still
choose to change the setting for a particular patient through the ECG parameter
advanced settings menu.
4-30

2042481-001
Revision C
Turn off system

Selection of this menu item brings up a dialogue window requesting you to
confirm your decision: CAUTION! This turns the system off. Are you sure you
want to do this?
Selecting yes powers off the Monitor. Selecting no returns the Monitor to the
Service Menu.
Service Mode Exit

To exit the Service Mode and power off the Monitor, locate and press the Power
hardkey at the front of the Monitor.
Revision C

2042481-001
4-31
4-32

2042481-001
Revision C
Revision C
Troubleshooting

2042481-001
5-1
For your notes
5-2

2042481-001
Revision C
Troubleshooting: Required Service Equipment
Required Service Equipment
Revision C
Multi Parameter Test Kit: MARQIII-KIT
Masimo Test Kit: 2021087-001
Oxymax Simulator: 2007650-002
ECG simulator (DNI model 214B or equivalent)
ECG cable (PN 412931-001, 411203-001, 411202-001)
SPO2 simulator (BIO-TEK SPO2 simulators)
SPO2 adapter cable and sensor (Masimo: 2016041-002,

Nellcor: DOC-10)
NIBP analyzer (DNI Nevada "CuffLink" or equivalent)
Adult Cuff (Critikon REF 2203)
Adult Hose (DASH type: 414873-001)
Adult mandrel, end block and spacer blocks (DNI PN 5215-0268, 5215-0269)
(Lead test)
Inflation bulb and associated tubing
Manometer Digital 0-600 mmHg range or equivalent
Temperature probe simulator (Alaris PN TE1811)
Temperature probe, oral (Alaris PN 3887)
Oscilloscope (capable of measuring ECG signal @ 0.75 Hz, 1 V amplitude)
1/8" stereo plug (Radio Shack PN 274-284C)
Safety Tester (DNI Nevada 235A or equivalent)
DMM (Fluke 8842 or equivalent)
Serial communication cable
Test plug assembly with 470 W resistor
Dash 2500 software download tool
Screw driver for Phillips cross head 1 and 2 screws

2042481-001
5-3
Troubleshooting: General Troubleshooting
General Troubleshooting
Problem
Solutions
No AC power
Check AC power
Faulty AC2DC power supply
Replace PSU module; FRU 2023852-011
Faulty DC2DC PWA
Replace DC2DC PWA; FRU 2023852-012
Faulty Main Board
Replace Main Board; FRU 2023852-007
Faulty cables
Replace defective cable; FRU 2023852-015
Faulty power off/on front

panel switch
Replace defective PWA keyboard; FRU

2023852-006
Faulty battery pack
Replace battery pack; FRU 2023852-029
Faulty DC2DC PWA
Faulty display
Replace LCD PANEL ASSY; FRU 2023852032
Faulty backlight driver
Replace INVERTER PWA; FRU 2023852-031
Faulty Main Board
Faulty DC2DC PWA
Faulty speaker assembly
Replace speaker assembly; FRU 2023852014
Faulty Main Board
Unit will not respond to

Trim Knob
Faulty encoder
Replace encoder; FRU 2023852-016
Faulty Main Board
Unit Host Comms not

functional
Faulty Main Board
Faulty DC2DC PWA
Unit will not power on
Unit will not operate

on battery
Unit powers on but no

display
Unit will not generate

sound
5-4
Cause

2042481-001
Revision C
Troubleshooting: Parameter Troubleshooting
Parameter Troubleshooting
Problem
Unit will not perform

NIBP function

ECG function
Unit will not produce

an analog ECG
waveform output
SpO2 function

TEMP function
Unit will not print
Revision C
Cause
Solutions
Faulty Main Board
Faulty pneumatics
assembly
Replace pneumatics assembly; FRU

2023852-010
Faulty pneumatics cable
Replace pneumatics assembly; FRU

2023852-010
Faulty front panel button
Replace defective keyboard PWA; FRU

2023852-006
Faulty DAS PWA assembly
Replace DAS box; FRU 2023852-049

(Nellcor SpO2)
Faulty ECG cable assembly
Replace ECG cable
Faulty Main Board
Faulty Defib cable

assembly
Replace Defib cable assembly
Faulty DC2DC PWA
Faulty Main Board

(Nellcor SpO2)
Faulty Main Board
Faulty temperature probe
Replace temperature proble

(Nellcor Spo2) or 2023852-050 (Masimo
Spo2)
Faulty Main Board
Unit out of paper or paper

incorrectly installed
Check paper installation
Faulty printer
Replace printer; FRU 2023852-008
Faulty Main Board
Faulty PSU module
Replace PSU module; FRU 2023852-011

2042481-001
5-5
Troubleshooting: Error Codes
Error Codes
Alarm Code Interpretation
If any other alarms appear that are not listed in the paragraphs that follow,
record the error message and report the failure to Customer Support. Refer to
the operation manual for information about patient alarms and general
procedural alarms.
For network modules troubleshooting, the information appear as the LED light in
the network module board, refer to Appendix F, LEDs .
System Failures
When a system failure is encountered, the error code is displayed on the screen
for 5 seconds and the system enters fail-safe mode. The error code is recorded
in the history log.
General system error codes are listed below. If any other SY or similar code
displays, report it to Customer Support.
System Error Messages

Error
5-6
Explanation
Possible Error Source
SY-16
Power fail signal true time is too long
Main CPU Board
SY-19
Software detected power supply out of limits failure
Main CPU Board
SY-20
Checksum of code in flash memory is not valid
Main CPU Board
SY-40
Unexpected interrupt
Main CPU Board
SY-43
Real time clock running stopped
Main CPU Board
SY-44
Real time clock running abnormal
Main CPU Board

2042481-001
Revision C
Hardware Error Messages

Error
Explanation
8193
HW, time base failure
Main CPU Board
8202
HW, power supply, system failure
Power Supply, Main

CPU Board
8222
HW, RAM test failure
Main CPU Board
8232
HW, ROM checksum failure
Main CPU Board
8252
HW, secondary processor not compatible
Main CPU Board
8253
HW, secondary communications failure
Main CPU Board
26631
Operating system 300 Hz timer re-entry error
Main CPU Board
27268
Unexpected error condition
Main CPU Board
NIBP Parameter Error Messages

Error
Revision C
Explanation
110
Overpressure circuit failure
Main CPU Board
130
EEProm read failure
Main CPU Board
131
EEProm write failure
Main CPU Board
140
Transducer initialization failure
Main CPU Board, Pneumatic Assembly
141
Calibration of a transducer channel's zero failed
142
Calibration of a transducer channel's span failed
150
Auto zero failure
180
Excessive leakage
Pneumatic Assembly, Interface Panel
190
Commands out of sequence
Main CPU Board
220
Valve in illegal state
221
Pressure too high for too long
227
Error calibration digital pot. Time out or setting not

within correct range

2042481-001
5-7
ECG Parameter Error Messages

Error
Explanation
101
MPDAS Board data rate error
MPDAS Board
102
MPDAS Board revision not compatible
MPDAS Board
103
MPDAS Board hardware error
MPDAS Board
109
Processing of ECG waveform too far behind
MPDAS Board, Main CPU Board
113
Data requested from ECG data manager is not available
MPDAS Board
114
Data requested from ECG data manager is not available
MPDAS Board
128
Errors returned while generating analog O/P
MPDAS Board
128-132
Errors returned while generating analog O/P
MPDAS Board
MPDAS Board command queue overrun
MPDAS Board
201
Temperature Parameter Error Messages

Error
5-8
Explanation
101
MPDAS Board
102
MPDAS Board
103
MPDAS Board
111
Software error-state machine bad probe number
MPDAS Board
120
TEMP type undefined
MPDAS Board

2042481-001
Revision C
SpO2 Parameter Error Messages

Error
Revision C
Explanation
Suggested Replacement
101
MPDAS Board
102
MPDAS Board
103
MPDAS Board
125
Too many reset requests
MPDAS Board,
Main CPU Board
126
Nellcor has posted a "serious" FE error
MPDAS Board
129
FE data OK- processing stalled
MPDAS Board
130
Masimo has posted either a board or diagnostic failure-type

available in Service Mode
MPDAS Board
131
Msg looks out of sequence
MPDAS Board
132
Missing characters inside a packet
MPDAS Board
133
Not able to correctly set parameter
MPDAS Board
134
NELL_SendCommand () called before previous call completed
MPDAS Board
135
Not enough room left in transmit FIFO to send data
MPDAS Board
136
Receive FIFO full, probably lost data
MPDAS Board
137
Queue out to OEM board is full
MPDAS Board
138
Nellcor has posted too many auto resets
MPDAS Board
139
Nellcor software error
MPDAS Board
140
Nellcor has posted too many communication errors
MPDAS Board
141
No communication with MPDAS board. Unit may be

configured incorrectly
MPDAS Board
150
Queue out to OEM board is full
MPDAS Board
151
Nellcor C-LOCK logic re-entered
MPDAS Board

2042481-001
5-9
Respiration Parameter Error Messages

Error
Explanation
101
This means something was wrong with memory at wake

up. Couldn't get data space.
MPDAS Board
These last three mean that the algorithm; execution

couldnt keep up with the data acquisition
MPDAS Board
102
103
104
Recorder Parameter Error Messages

Error
5-10
Explanation
Suggested Replacement
101
Output (to printer) queue overflow
Printer
102
Printer
103
Printer
104
Input queue (from system) overflow
Printer
105
Queue freeze error
Printer
110
Invalid speed setting
Printer
111
Invalid number of waves setting
Printer
112
Invalid density setting
Printer
114
Bad command
Printer
115
Bad command
Printer
120
Queue not initialized
Printer
121
Annotation queue overflow
Printer
122
Invalid location
Printer
123
Not enough room
Printer
140
Bad command for this mode
Printer
141
Bad command for this mode
Printer

2042481-001
Revision C
Revision C
Field Replaceable
Units

2042481-001
6-1
For your notes
6-2

2042481-001
Revision C
Field Replaceable Units: Ordering Parts
Ordering Parts
The parts lists and drawings in this chapter supply enough detail for you to order
parts for the assemblies considered field replaceable.
If you require additional information or troubleshooting assistance, contact GE
Technical Support.
To order parts, contact Service Parts at the address or telephone number listed
on the How to Reach Us... page found in service manual CD.
For the latest parts information, including substitutions, obsolescence, and
compatibility, please contact you local GE service provider.
Revision C

2042481-001
6-3
Field Replaceable Units: Parts
Parts
The table below lists field replaceable units that can be ordered.
NOTE:
Due to recent branding changes, the part ordered may vary slightly from
the previous part. Contact you local GE service provider for a full list of
available parts
Find Number
6-4
Item Number
Item Description
633176
BATTERY, 3.6V, PWB
2023852-002
FRU, DASH 2500, PLASTIC FRONT CASE
2023852-049
FRU, DASH 2500 V3, DAS NELLCOR
2023852-050
FRU, DASH 2500 V3, DAS MASIMO
2023852-005
FRU, DASH 2500, TURBO TEMP
2023852-006
FRU, DASH 2500, PWA KEYBOARD
2023852-007
FRU, DASH 2500, PWA MAIN BOARD
2023852-008
FRU, DASH 2500, PRINTER
2023852-009
FRU, DASH 2500, RECORDER ROLLER
10
2023852-010
FRU, DASH 2500, PNEUMATIC ASSY KIT
11
2023852-011
FRU, DASH 2500, PSU MODULE ASSY
12
2023852-012
FRU, DASH 2500, DC2DC PWA
13
2023852-013
FRU, DASH 2500, FAN ASSY
14
2023852-014
FRU, DASH 2500, SPEAKER ASSY
15
2023852-015
FRU, DASH 2500, CABLES
16
2023852-016
FRU, DASH 2500, TRIM KNOB
17
2023852-051
FRU, DASH 2500, SCREW-LOCK SCREW
18
2023852-018
FRU, DASH 2500, LABEL SET ENGLISH
19
2023852-019
FRU, DASH 2500, LABEL SET CHINESE
20
2023852-020
FRU, DASH 2500, LABEL SET FRENCH
21
2023852-021
FRU, DASH 2500, LABEL SET GERMAN
22
2023852-022
FRU, DASH 2500, LABEL SET ITALIAN
23
2023852-023
FRU, DASH 2500, LABEL SET SPANISH

2042481-001
Revision C
Field Replaceable Units: Parts
Find Number
Revision C
Item Number
Item Description
24
2023852-025
FRU, DASH 2500, LABEL SET PORTUGUESE
25
2023852-026
FRU, DASH 2500, LABEL SET HUNGARIAN
26
2023852-027
FRU, DASH 2500, LABEL SET RUSSIAN
27
2023852-028
FRU, DASH 2500, LABEL SET POLISH
28
2023852-029
FRU, DASH 2500, BATTERY
29
2023852-030
FRU, DASH 2500, HARDWARE KIT
30
2023852-031
FRU, DASH 2500, INVERTER PWA
31
2023852-032
FRU, DASH 2500, LCD PANEL ASSY
32
2023852-037
FRU, DASH 2500, PLASTIC REAR CASE
33
2023852-039
FRU, DASH 2500, LABEL SET CZECH
34
2023852-040
FRU, DASH 2500, LABEL SET DANISH
35
2023852-041
FRU, DASH 2500, LABEL SET GREEK
36
2023852-042
FRU, DASH 2500, LABEL SET SWEDISH
37
2023852-043
FRU, DASH 2500, LABEL SET FINNISH
38
2023852-044
FRU, DASH 2500, LABEL SET DUTCH
39
2023852-045
FRU, DASH 2500, LABEL SET ROMANIAN
40
2023852-046
FRU, DASH 2500, LABEL SET TURKISH
41
2023852-047
FRU, DASH 2500, LABEL SET NORWEGIAN
42
2023852-048
FRU, DASH 2500, LABEL SET KOREAN
43
2023852-052
FRU, DASH 2500, SOFTWARE CD
44
2023852-054
FRU, DASH 2500, NETWORK MODULE
45
2023852-056
FRU, DASH 2500, OP MNL/LABEL CN

2042481-001
6-5
Field Replaceable Units: Assembly Drawings
Assembly Drawings
The assembly drawings below indicate the field replaceable parts.
6-6

2042481-001
Revision C
Revision C

2042481-001
6-7
6-8

2042481-001
Revision C
Revision C

2042481-001
6-9
6-10

2042481-001
Revision C
Revision C

2042481-001
6-11
6-12

2042481-001
Revision C
Field Replaceable Units:
Revision C

2042481-001
6-13
Field Replaceable Units: Disassembly Guidelines
Disassembly Guidelines
REPAIR TO THE FRU LEVEL Field repairs are recommended to the field
replaceable unit (FRU) only. Attempting a field repair on a PCB or a factory
sealed component or assembly could jeopardize the safe and effective
operation of the Monitor.
DAS ASSEMBLY Do NOT open the DAS assembly as this breaks the isolation
barrier which may result in patient death or serious injury. The DAS assembly is
a field replaceable unit only. There are NO field repairs or adjustments for the
DAS assembly.
DC2DC ASSEMBLY When removing the GCX plate from the bottom of the
Monitor, clearly identify the screws to ensure the same screws are used to
replace the GCX plate. Screws that are too long will penetrate into the DC2DC
assembly and cause the battery to split or break.
NOTE:
GE recommends that you assemble the Monitor using the NEW fasteners
(screws, washers, etc.) provided in the FRU Kits. Some fasteners, like the
screws with a thread locking coating, are NOT intended to be re-used more
than three times.
Tools Required
A standard set of hand tools is required for disassembly and assembly.
Before Disassembly
Before you disassemble the Monitor, you should ALWAYS do the following tasks.
6-14
1.
Unplug the monitor.
2.
Remove the battery.
3.
Provide appropriate electrostatic discharge protection to prevent damaging

the Monitor.
4.
Be aware that the nonspecific disassembly instructions apply to all monitors

supported by this service manual. Disassembly for specific models of the
Monitor are identified when required.

2042481-001
Revision C
Field Replaceable Units: Disassembly Guidelines
Hardware Precautions
When disassembling the Monitor, observe the following guidelines:
Remove the handle assembly, then remove the display assembly to access
the field replaceable units of the display assembly and the main unit.
Note the positions of wires, cables, and different sized screws; marking them
if necessary to ensure they are replaced correctly.
DO NOT kink, pinch, stretch, twist, or tightly fold a flex cable.
Unless otherwise stated, reassemble the Monitor in reverse order of

disassembly.
Electrostatic Discharge (ESD) Precautions

All external connector inputs and outputs of the Monitor are designed with
protection from ESD damage. However, if the Monitor requires service, exposed
components and assemblies contained within are susceptible to ESD damage.
This includes human hands, non-ESD protected work stations and/or improperly
grounded test equipment.
The following guidelines help make a service workstation more resistant to ESD
damage:
Discharge any static charge you may have built up before handling
semiconductors or assemblies containing semiconductors.
A grounded, antistatic wristband (3M PN 2046 or equivalent) or heel strap

should be worn at all times while handling or repairing assemblies
containing semiconductors.
Use properly grounded soldering and test equipment.
Use a static-free work surface (3M PN 8210 or equivalent) while handling or

working on assemblies containing semiconductors.
DO NOT remove semiconductors or assemblies containing semiconductors

from antistatic containers (Velo-stat bags) until absolutely necessary.
Make sure power to an assembly is turned off before removing or inserting a

semiconductor.
DO NOT slide semiconductors or electrical/electronic assemblies across any

surface.
DO NOT touch semiconductor leads unless absolutely necessary.
Semiconductors and electrical/electronic assemblies should be stored only

in antistatic bags or boxes.
Handle all PCB assemblies by their edges.
DO NOT flex or twist the circuit board.
These guidelines may not guarantee a 100% static-free workstation, but can
greatly reduce the potential for failure of any electrical/electronic assemblies
being serviced.
Revision C

2042481-001
6-15
Field Replaceable Units: Remove/Replace Battery
Remove/Replace Battery
6-16
1.
Remove the four M5 screws with the driver, then take off the aluminium
plate.
2.
Take off the plastic cover.
3.
Release the lock and then take out the battery and wires.
4.
Replace the battery.

2042481-001
Revision C
Field Replaceable Units: Replace Plastic Front Case
Replace Plastic Front Case
Revision C
1.
Remove the temperature module first.
2.
Remove all the six screws from rear case. The unit is separated into front
case and rear case.
3.
Take off the four different wires and replace the front case.

2042481-001
6-17
Field Replaceable Units: Replace Main Board Assembly
Replace Main Board Assembly

1.
Separate the front case and the rear case, then remove the four screws and
take the Main Board out of rear case.
2.
Pull out all tubes that are connected to the Main Board and replace the
Main Board. Connect the jumper to the Main Board as indicated in the
following graphic.
3.
Connect all the tubes to the Main Board as indicated in the following
graphics.
Tube Connection
6-18

2042481-001
Revision C
Field Replaceable Units: Replace DAS Board Assembly
Replace DAS Board Assembly

1.
Remove the recorder assembly first.
2.
Remove the four screws from the rear case assembly and take out the
chassis assembly.
3.
Pull out the DAS assembly and replace with the new DAS assembly. There
are two DAS assemblies to select: DAS assembly with NELLCOR SpO2 or
DAS assembly with MASIMO SpO2.
Revision C

2042481-001
6-19
Field Replaceable Units: Replace DC2DC Board Assembly
Replace DC2DC Board Assembly
6-20
1.
Remove AC2DC board first.
2.
Pull out the grounding cable from the DC2DC PWA.
3.
Remove the four screws and replace the DC2DC PWA.

2042481-001
Revision C
Field Replaceable Units: Replace AC2DC Board Assembly
Replace AC2DC Board Assembly
Revision C
1.
Disconnect the three cables.
2.
Remove the four screws.
3.
Replace the AC2DC assembly.

2042481-001
6-21
Field Replaceable Units: Replace Keyboard and Trim Knob
Replace Keyboard and Trim Knob
6-22
1.
Remove the inverter board and disconnect the cables.
2.
Remove all the six screws and take out the LCD assembly.
3.
Replace either the left or the right keypad PWA.
4.
Take out the gasket, then use a sleeve to get the corder out. Replace it with
the new corder and replace the knob.

2042481-001
Revision C
Field Replaceable Units: Replace the Invert Board
Replace the Invert Board
Revision C
1.
Pull out the cables and remove all the four screws.
2.
Replace the invert board.

2042481-001
6-23
Field Replaceable Units: Replace the AC Inlet
Replace the AC Inlet
6-24
1.
Remove the two screws and take out the AC Inlet.
2.
Remove the grounding screw.
3.
Replace the AC Inlet.

2042481-001
Revision C
Field Replaceable Units: Replace the Speaker
Replace the Speaker

1.
Pull out the printer holder and slip out the foam gasket.
2.
Replace speaker.
3.
Stick the new foam gasket to the speaker.
Replace the printer
Revision C
1.
Remove the two screws.
2.
Replace the printer

2042481-001
6-25
Field Replaceable Units: Replace the Pneumatic Pump
Replace the Pneumatic Pump

1.
Cut off the cable straps.
2.
Replace the pneumatic pump.
3.
Tie the replaced pump with new cable straps.
Replace the Check Valve
6-26
1.
Cut off the cable straps.
2.
Replace the check valve.
3.
Tie the check valve with new cable straps.

2042481-001
Revision C
Field Replaceable Units: Replace the Fan
Replace the Fan
Revision C
1.
Remove all the screws and pull out the cable.
2.
Replace the fan.

2042481-001
6-27
Field Replaceable Units: Assemble Network Module
Assemble Network Module

The Dash 2500 network module is installed inside the interface cover.
6-28
1.
Remove the screw and open the interface cover.
2.
If the monitor is the old version, replace the ports two screws into new
screw-locks, with the 5mm hexagonal socket wrench.
3.
Connect the network module board into the port

2042481-001
Revision C
Field Replaceable Units:

4.
Install the three screws
5.
Close the interface cover.
After Assembly
Perform the Electrical Safety Tests and Checkout Procedures after assembly to
ensure the Monitor with new FRUs work functionally. Refer to Chapter 4 and
Appendix B for details.
Revision C

2042481-001
6-29
Field Replaceable Units: After Assembly

For your notes
6-30

2042481-001
Revision C
Revision C
Technical
Specifications

2042481-001
A-1
For your notes
A-2

2042481-001
Revision C
Technical Specifications: Technical Specifications
Technical Specifications
Due to continual product innovation, specifications are subject to change
without notice. The following specifications are accurate as of the date of this
publication, and pertain to the Monitor
General Specifications
Specifications
Mechanical
Monitor
8.7 in (H) x 6.7 in (D) x 14.1 in (W)

22.0 cm (H) x 17.0 cm (D) x 35.8cm (W)
Weight
12 lb (5.5 kg)
Environmental*
Operating Temperature
41F to 104F (5C to 40C)
Storage and Transportation

Temperature
-4F to 140F (-20C to 60C)
Operating Humidity
5% to 95% noncondensing

Humidity
5% to 95% noncondensing
Operating Atmospheric
Pressure
700 hPa to 1060 hPa

Atmospheric Pressure
500 hPa to 1060 hPa
Electrical
AC Input Voltage
100-240 V
AC Input Frequency
50/60 Hz
AC Input Power
120 VA
Internal Battery
8.4 V nickel-metal-hydride (NiMH)
Power Supply
The Dash 2500 Patient Monitor can be powered from the internal battery or AC
power.
Battery
An internal, rechargeable battery pack powers the Monitor for greater than 180
minutes at a specified load. The battery typically charges to full capacity within 4
hours when power off.
* The Monitor may not meet Performance Specifications (ANSI/AAMI SP10) if it is stored or used outside of the specified ranges of environmental
parameters.
Revision C

2042481-001
A-3
Specifications
Power Cable
The power cable is detachable.
Fuses
Internal
FS1
0.5 amp, 60V, auto-reset
FS2
FS3
10 amp, 250V, fast acting, not resettable
FS4
FS5
External
FS
1amp, 250V, not resettable
FS
1amp, 250V, not resettable
A-4

2042481-001
Revision C
NIBP Specifications
Specifications
Method
Oscillometric with step deflation
Modes
Manual, automatic, stat
BP Measurement Ranges
Systolic
30 to 290 mmHg (adult/pediatric)

4.0 to 38.7 kPa (adult/pediatric)
30 to 140 mmHg (neonate)
4.0 to 18.7 kPa (neonate)
MAP

Diastolic

Resolution
1 mmHg
Accuracy
Meets AAMI/ANSI standard SP10:2002
Initial Cuff Inflation Pressure
135 15 mmHg default; user selectable (adult/pediatric)

100 15 mmHg default; user selectable (neonate)
Maximum Determination Time
120 s (adult/pediatric)
85 s (neonate)
Over Pressure Monitor

Pulse Rate
When NIBP is the source, HR values are derived from the pulserate
that is determined by the oscillometric technique of measuring
blood pressure. The rate source field is labeled NIBP.
Adult/Pediatric Range: 30 to 200 bpm ( 3.5% or 3 bpm)
Neonate Range: 30 to 220 bpm ( 3.5% or 3 bpm)
GE Healthcare Patents
4,638,810; 5,052,397; 4,754,761; 5,170,795; 6,188,407; 5,357,970; 5,704,362;
5,680,870; 5,518,000; 6,893,403; 6,423,010; 6,358,213; 5,704,362; 5,579,776 and
international equivalents. US patents pending.
Revision C

2042481-001
A-5
NELLCOR OXIMAX SpO2 Specifications

Specifications
Measurement Range
SpO2
1 to 100%
Pulse Rate
20 to 250 bpm
Perfusion Range
0.03 to 20%
Accuracy
Saturation
Adult*
70 to 100% 2 digits
Neonate*
70 to 100% 3 digits
Low Perfusion**
70 to 100% 2 digits
Pulse Rate
Adult and Neonate
20 to 250 bpm 3 digits
Low Perfusion**
*Adult specifications are shown for OxiMaxMAX-A and MAX-N sensors with the N-600. Saturation accuracy will vary by sensor type.
**Applicability: OxiMax MAX-A, MAX-AL, MAX-P, MAX-I, and MAX-N sensors.
Specifications: NELLCOR OXIMAX Sensor Accuracy

NOTE: All NELLCOR OXIMAX sensors must be used with the NELL1 GE cable; the SCP-10 cable. RS-10 and
Oxisensor II sensors are not compatible with the Dash 2500 Patient Monitor.
SpO2 Range
70% - 100%
Sensor Model
OXIMAX
MAX-A, MAX-AL
2 digits
MAX-N (Adult)
2 digits
MAX-N (Neonate)
3 digits
MAX-P
2 digits
MAX-I
2 digits
MAX-FAST
2 digits
SC-A (Adult)
2 digits
SC-PR (Neonate)
3 digits
A-6

2042481-001
Revision C
Specifications: NELLCOR OXIMAX Sensor Accuracy

3.5 digits
MAX-R
OxiCliq
OxiCliq A
2.5 digits
OxiCliq P
2.5 digits
OxiCliq N (Adult)
2.5 digits
OxiCliq N (Neonate)
3.5 digits
OxiCliq I
2.5 digits
Reusable Sensor Models

D-YS (Infant to Adult)
3 digits
D-YS (Neonate)
4 digits
D-YS & D-YSE
3.5 digits
D-YS & D-YSPD
3.5 digits
DS-100A
3 digits
OXI-A/N (Adult)
3 digits
OXI-A/N (Neonate)
4 digits
OXI-P/I
3 digits
Neonatal Sensor Accuracy
When sensors are used on neonatal subjects as

recommended, the specified accuracy range is increased
by 1 digit, as compared to adult usage, to account for
the theoretical effect on oximeter measurements of fetal
hemoglobin in neonatal blood. For example, MAX-N
accuracy on neonates is 3 digits, rather than 2 digits.
Sensor Light Source

Wavelength
Infrared: 890 nm (nominal)

Red: 660 nm (nominal)
Power Dissipation
Infrared: 22.5 mW (max)

Red: 30 mW (max)
The MAX-N, D-YS, OXI-A/N, and OxiCliq N were tested on patients >40 kg.
The accuracy specification has been determined between saturations of 80%-100%.
NELLCOR Puritan Bennett, Inc. Patents

4,621,643; 4,653,498; Re.35,122; 4,700,708; 4,770,179; 4,802,486; 4,869,254;
4,928,692; 4,934,372; 5,078,136; 5,351,685; 5,421,329; 5,485,847; 5,533,507;
5,577,500; 5,803,910; 5,853,364; 5,865,736; 6,083,172 and international
equivalents.
Revision C

2042481-001
A-7
MASIMO SET SpO2 Specifications

Specifications
Measurement Range
SpO2
1 to 100%
Pulse Rate
25 to 240 bpm
Perfusion Range
0.02 to 20%
Accuracy and Motion Tolerance

Saturation
Without Motion - Adult/Pediatric*
70 to 100% 2 digits
Without Motion - Neonate*
70 to 100% 3 digits
With Motion - Adult/Pediatric/Neo**
70 to 100% 3 digits
Low Perfusion
70 to 100% 2 digits
0 to 69% unspecified
Pulse Rate
Without Motion
With Motion
normal physiologic range

* The MASIMO SET SpO2 parameter with LNOP-Adt sensors has been validated for no motion accuracy in human blood studies on healthy adult
volunteers in induced hypoxia studies in the range of 70-100% SpO2 against a laboratory co-oximeter and ECG monitor. This variation equals plus
or minus one standard deviation. Plus or minus one standard deviation encompasses 68% of the population.
**The MASIMO SET SpO2 parameter with LNOP-Adt sensors has been validated for motion accuracy in human blood studies on healthy adult
volunteers in induced hypoxia studies while performing rubbing and tapping motions at 2 to 4 Hz at an amplitude of 1 to 2 cm and a nonrepetitive
motion between 1 to 5 Hz at an amplitude of 2 to 3 cm in induced hypoxia studies in the range of 70-100% SpO2 against a laboratory co-oximeter
and ECG monitor. This variation equals plus or minus one standard deviation. Plus or minus one standard deviation encompasses 68% of the
population.
The MASIMO SET SpO2 parameter with LNOP-Neo Pt sensors has been validated for neonatal motion accuracy in human blood studies on
neonates while moving the neonates foot at 2 to 4 cm against a laboratory co-oximeter and ECG monitor. This variation equals plus or minus, one
standard deviation. Plus or minus one standard deviation encompasses 68% of the population.
The MASIMO SET SpO2 parameter has been validated for low perfusion accuracy in bench top testing against a Biotek Index 2 simulator and
MASIMOs simulator with signal strengths of greater than 0.02% and a % transmission of greater than 5% for saturations ranging from 70 to
100%. This variation equals plus or minus, one standard deviation. Plus or minus one standard deviation encompasses 68% of the population.
NOTE: Note: LNCS sensors using LNCS cable technology offer nearly the same performance as the LNOP flexcircuit design. The LNOP single patient sensor line is still the industry "gold standard", while LNCS is the best
cabled sensor alternative.
A-8

2042481-001
Revision C
Specifications: MASIMO Sensor Accuracy

SpO2 Range
70% - 100%
Sensor Model
LNOP
LNOP-ADT
2 digits
LNOP-ADT Long
2 digits
LNOP-PDT
2 digits
LNOP-NEO
3 digits
LNOP-NEO PT
3 digits
LNOP-DCI (reusable)
2 digits
LNOP-DCSC (reusable)
2 digits
LNOP-DCIP (reusable)
2 digits
NRI25 (reusable)
2 digits
Resolution
Saturation (% SpO2)
1%
Pulse Rate (bpm)
Low Perfusion Performance

0.02% Pulse Amplitude
Saturation (% SpO2) 2 digits
and% Transmission >5%
Pulse Rate 3 digits
Interfering Substances
Carboxyhemoglobin may erroneously increase

readings. The level of increase is approximately
equal to the amount of carboxyhemoglobin
present. Dyes, or any substance containing
dyes, that change usual arterial pigmentation
may cause erroneous readings.
Sensor Light Source

Wavelength
Infrared: 905 nm (nominal)

Red: 660 nm (nominal)
Power Dissipation
Infrared: 22.5 mW (max)

Red: 27.5 mW (max)
MASIMO Patents
5,482,036; 5,490,505; 5,632,272; 5,685,299; 5,758,644; 5,769,785; 6,002,952;
6,036,642; 6,067,462; 6,157,850; 6,206,830; 6,263,222 and international
equivalents.
Revision C

2042481-001
A-9
ECG Specifications
Specifications
Leads available
3-electrode configuration: I, II, III

5-electrode configuration: I, II, III, aVR, aVL, aVF, and
VA
QRS amplitude range
0.5 to 5.0 mV
Heart rate accuracy
30 to 300 bpm
3 bpm or 3% of reading, whichever is greater
Heart rate resolution
1 bpm
Bandwidth
0.5 to 40 Hz +1/-6 dB
0.05 to 40 Hz +1/-6 dB
0.05 to 100 Hz +1/-6 dB
Standardizing voltage
1 mV marker
Common mode rejection
1 mV RTI or 10 mm p-p max displayed noise allowed

with 20 Vrms, 50-60 Hz input
Input Impedance
Common mode
Differential
> 2.5 M at 10 Hz
> 2.5 M from DC to 60 Hz
60 Hz tolerance
up to 10 mV
Pacemaker detection/rejection
Input voltage range
2 mV to 700 mV
Tall T wave rejection
100% @ 0.05 to 40Hz or 0.05 to 100Hz

80% @ 0.5 to 40Hz
Lead off sensing current
< 0.1 A DC signal leads

< 1 A DC driven lead
Time to alarm
high heart rate < 10 s per AAMI EC13 - 2002

low heart rate < 10 s per AAMI EC13 - 2002
cardiac standstill < 10 s per AAMI EC13 - 2002
tachycardia waveforms < 10 s per AAMI EC13 - 2002
ANSI/AAMI EC13-2002 Section 4.1.2.1 d). The Heart Rate Averaging computation is as follows, the average of the
last 8 R-to-R intervals, the update rate of the Heart Rate on the display is once per second.
When tested in accordance with ANSI/AAMI EC13-2002 Section 4.1.2.1f), the response time of the heart rate
meter to changes in heart rate is:
Step increase from 80 to 120 BPM
Step decrease from 80 to 40 BPM
average 6.75 sec, range 6.5 to 7.3 sec

average 10.04 sec, range 8 to 11 sec
When tested in accordance with ANSI/AAMI EC13-2002 Section 4.1.2.1g), the time to alarm for ventricular
tachycardia is:
For Figure 4a
A-10
averages range from 5 to 9 seconds with individual

values ranging from 4 to 11 seconds.

2042481-001
Revision C
Specifications
For Figure 4b
averages range from 5 to 8 seconds with individual

values ranging from 4 to 11 seconds
When tested in accordance with ANSI/AAMI EC13-2002 Section 4.1.4.3), the minimum input slew rate that will
cause approximately 50% of the pulses to trigger the pacer pulse detector is:
For Figure 5d
3.33 v/s RTI, +/- 10%
When tested in accordance with ANSI/AAMI EC13-2002 Section 4.1.2.1e), the heart rate after a 20 second
stabilization period is:
For Figure 3a
1X size setting: not detect

2X size setting: 80 + 3 bpm
For Figure 3b

For Figure 3c

For Figure 3d
1X size setting: not detect

2X size setting: 90 + 9bpm
RESP Specifications
Specifications
ECG-Derived Respiration Rate
Leads available
I or II
Range
6 to 120 breaths/min (adult/pediatric)

6 to 180 breaths/min (neonate)
Accuracy
2 breaths/min or 3%
of reading; whichever is greater
Resolution
1 breath/min
Base Impedance
100 to 2000
Detection Sensitivity
0.2 @ 30 breath/min with 500 baseline impedance
Excitation Frequency
65.5 kHz
Amplitude
Revision C
< 300 A rms

2042481-001
A-11
HR/Pulse Specifications
Specifications
ECG
Heart rate accuracy
30 to 300 bpm
3 bpm or 3% of reading, whichever is greater
Time to alarm
high heart rate < 10 s per AAMI EC13 - 2002

low heart rate < 10 s per AAMI EC13 - 2002
cardiac standstill < 10 s per AAMI EC13 - 2002
tachycardia waveforms < 10 s per AAMI EC13 - 2002
NELLCOR SpO2
Range
20 - 250 bpm
Accuracy and Tolerance
Low Perfusion
MASIMO SpO2
Range
25 - 240 bpm
Accuracy and Motion Tolerance

Without Motion
With Motion
normal physiologic range

Noninvasive Blood Pressure

Range
Adult/ped
30 - 200 bpm
Neonate
30 - 220 bpm
Accuracy
3.5%
Alarm Limits
Range
A-12
30 - 250 bpm

2042481-001
Revision C
TURBO TEMP Specifications

Specifications
Scale
Fahrenheit (F)
Celsius (C)
Predictive Mode
Range
96.0F (35.6C) to 106.0F (41.1C)
Resolution
0.1F (0.1C)
Monitor Mode
Range
80.0F (26.7C) to 108.0 F (42.2C)
Accuracy
0.2F ( 0.1C) (when tested in a calibrated liquid bath; meets

ASTM E1112, Table 1, in range specified)
Resolution
0.1F (0.1C)
Probes
CAUTION:
Use only Alaris probes and probe covers. The size, shape, and
thermal characteristics of the probe covers can affect the
performance of the instrument. Inaccurate readings or retention
problems may occur unless Alaris probes and probe covers are
used.
Determination Time
Approx. 10 seconds, typical
Alaris Patents
D,300,728; D,300,909 and other pending patent.
Revision C

2042481-001
A-13
A-14

2042481-001
Revision C
Revision C
Test Record

2042481-001
B-1
For your notes
B-2

2042481-001
Revision C
Test Record
Model ____________
TEST RECORD
Serial ____________
Description
Min
Max
Actual
Pass
Fail
N/A
Safety Testing
AC mains ground pin to earth ground resistance ()
0.1
Normal no-fault leakage (A)
500
Normal open-ground leakage (A)
500
Normal open-neutral leakage (A)
500
Reverse no-fault leakage (A)
500
Reverse open-ground leakage (A)
500
Reverse open-neutral leakage (A)
500
Patient (Source) Leakage CurrentECG-Normal no-fault leakage (A)
10
ECG-Normal open-ground leakage (A)
50
ECG-Reverse no-fault leakage (A)
10
ECG-Reverse open-ground leakage (A)
50
Spo2-Normal no-fault leakage (A)
100
Spo2-Normal open-ground leakage (A)
500
Spo2-Reverse no-fault leakage (A)
100
Spo2-Reverse open-ground leakage (A)
500
Temp-Normal no-fault leakage (A)
100
Temp-Normal open-ground leakage (A)
500
Temp-Reverse no-fault leakage (A)
100
Temp-Reverse open-ground leakage (A)
500
Patient (Sink) Leakage CurrentECG-Normal Single-fault leakage (A)
50
ECG-Reverse Single-fault leakage (A)
50
Spo2-Normal Single-fault leakage (A)
Spo2-Reverse Single-fault leakage (A)
Temp-Normal Single-fault leakage (A)
Temp-Reverse Single-fault leakage (A)
SpO2 reading at 98% Saturation
96
100
BPM reading at 80 BPM
76
84
SpO2 Testing
Revision C

2042481-001
B-3
Test Record
Description
Min
Max
Actual
Pass
Fail
N/A
NIBP Testing (Perform in Service Mode)

Leakage Test
UUT Pressure - 50 mmHg
47
53
147
153
247
253
Verify adult overpressure occurs between 300~330 mmHg
300
330
Verify neo overpressure occurs between 150~165 mmHg
150
165
Initial cuff inflation (Adult cuff)
161
195
Systolic Reading (120/80 Adult)
107
133
Diastolic Reading (120/80 Adult)
67
93
Heart Rate reading @ 80 BPM (NIBP)
76
84
Initial cuff inflation (Neonatal cuff)
94
151
Systolic Reading (100/65 Neonatal)
87
123
Diastolic Reading (100/65 Neonatal)
52
78
Verify HR LOW alarm and BPM at 30
26
34
Verify HR HIGH alarm and BPM at 160
156
164
Verify ECG VTACH alarm and BPM at 180
176
184
Verify RESP (@ 20 BPM)
17
23
Verify RESP (@ 60 BPM)
57
63
Inflate/ Deflate cycle time <120 seconds
ECG Testing (Perform in Monitor Mode)

Verify Waveform
Verify paced 1 marker on ECG signal
Verify paced 2 marker on ECG signal
Verify ECG LEAD FAIL alarm

RESP Testing (Perform in Monitor Mode)
Verify Waveform
B-4

2042481-001
Revision C
Test Record
Description
Min
Max
Actual
Pass
Fail
N/A
Temperature Testing (Perform in Service or Monitor Mode - requires Alaris Temp Simulator)
Measured Temp in F (98.6 nominal)
98.4
98.8
79.9
80.5
107.5
108.1
Voltage between pins 4 and 8, alarm inactive
4.7
5.3
Voltage between pins 4 and 8, alarm active
0.0
0.1
Probe Disconnected
Probe Type
Probe In/Out Detect
Recorder Testing
Recorder Test
Battery System Testing (Perform in Monitor Mode)
Verify AC Mains Indicator
Remove AC, Verify uninterrupted battery operation
Verify Battery LED is lit
Fail-safe Logic Testing
Fail-safe Logic
Keypad Key Testing (Perform in Service Mode)
Verify appropriate responses to key presses
Sound Testing
Speaker Test
Communications Testing
Verify pump starts, stops and temp status returns
Remote Alarm Testing
Network Testing
Verify network communication
Tested By:
Date:
Signature:
Facility:
Revision C

2042481-001
B-5
Test Record
B-6

2042481-001
Revision C
Revision C
Configuration

2042481-001
C-1
For your notes
C-2

2042481-001
Revision C
Configuration: Monitor Configuration Mode
Monitor Configuration Mode

Enter Configuration Mode
1.
Select other system settings from the Main Menu.
2.
Select go to config mode. The message, This will initiate the sequence for
entering Configuration Mode. Do you want to do this? appears.
3.
Select Yes to enter configuration mode.
4.
The message, Please enter the Config Mode password. appears. Enter the
password. FACTORY SET CONFIG PASSWORD: 2508.
5.
Select Done.
6.
The system will restart in configuration mode. Press the Trim Knob to access
the Configuration Menu.
Configure Default Changes
Revision C
1.
Select admit patient from the Configuration Menu.
2.
Select Choose patient settings. Selections are ADULT, PEDIATRIC and

NEONATE. Select the patient type.
3.
A popup window appears: All unsaved changes to the current default will
be lost! Are you sure you want to do this? Select Yes.
4.
Change all other available settings as desired.
5.
To save your changes for the selected table, go to other system settings,
select save default changes. The default changes are saved.

2042481-001
C-3
Exit Configuration Mode

1.
Select other system settings from the Configuration Menu.
2.
Select exit config mode.
3.
A popup window appears: This will exit configuration mode. All unsaved
changes will be lost. Are you sure you want to do this? Select Yes.
4.
The system will automatically restart in patient monitoring mode.

WARNING
All monitoring will cease when entering configuration mode.
Do not enter this mode if actively monitoring a patient.
C-4

2042481-001
Revision C
Revision C

2042481-001
numbers
User can choose whether to view trended derived vital signs data in the Full
trends window either numerically or graphically. When the Full trends window
is opened, the configured default becomes the confirmed selection of this
choice.
Display as
blank
0 chosen
This opens a data entry dialog with the text Enter Unit Number.
enter unit number
blank
ADULT
N/A
Choose graphs to print
This opens a data entry dialog box with the text Enter Bed Number.
enter bed number
It allows the user to choose a user default table.
Allows the user to discharge a patient.
Confirmed selections are printed on the bedside recorder when print chosen
graphs is chosen. If there are no confirmed selections for this choice when
print chosen graphs is confirmed, up to two selections are automatically
confirmed. The selections automatically confirmed are the highest priority
parameters included in the confirmed patients parameter list, up to a
maximum of two.
View Patient Trends
Choose Patient settings
discharge
It allows the user to adjust the length of time alarms are temporarily silenced
when the alarm silence feature is activated.
Alarm silence time (in min)
Admit Patient
N/A
N/A
It allows the user to autoset all currently operating parameter alarm limits
around the patient's current condition using the percentage confirmed in
Choose autoset %
It opens the Config Adjust Alarms menu.
20%
It allows the user to change the percentage at which limits are automatically
adjusted around the patient's current condition when the autoset all is
confirmed.
It allows the user to adjust the alarm volume. Alarm volume applies to all
alarms (excluding system failures).
Factory Default
It allows the user to specify the lowest range for which the alarm volume can
be adjusted.
autoset all
Choose autoset %
Adjust alarm volume
Understanding the Options
Alarm volume low range
Config settings
Adjust Alarms
Default Table Name
Adult
Pediatric
Neonate
C-5
C-6
N/A
yes
numbers
1 min/50 min
It allows the user to turn on or off the viewing of the Mini trends window in the
waveform region of the main monitoring screen.
User can choose whether to view trended derived vital signs data in the Mini
trends window either numerically or graphically.
View vitals every is displayed when Display as in Mini trends is numbers. It
allows the user to choose the set of viewable times for the Mini trends window.
View vitals for is displayed when Display as in Mini trends is graphs. It allows
the user to choose the span of time to be viewed in the Mini trends window.
View trends on main screen?
Display as
View vitals every/View vitals for
User specifies which window (either Full trends or Mini trends) that the hardkey
activates/deactivates.
Trend key default

2042481-001
User specifies audio alarm associated with limit alarms.
User specifies if HR/Pulse vital sign area color is based on current heart rate
source or configured color choice in HR/Pulse parameter.
User specifies the color for information related to HR/Pulse that is displayed in
the Limit and Full and Mini trends windows.
Change color based on source?
Select HR/Pulse's color
It opens the Advanced Setup HR/Pulse menu.
Limit alarms priority
Advanced settings...
Allows the user to set the "lo" alarm limit.
lo
Patient alarm limits may be adjusted by the auto-set feature or manually.
Adjust limits
Allows the user to set the "hi" alarm limit.
User specifies the volume for the QRS beep relative to the other volume
settings for alarms and key clicks.
Adjust QRS volume
hi
User specifies the source from which HR/Pulse rate is to be derived.
Select source
Setup HR/Pulse
yes
User specifies whether Select Patient is available or unavailable in clinical

mode.
Save previous patient data?
green
yes
warning
N/A
A=50, P=60
A=150, P=160
auto-set
auto
mini trends
N/A
It opens the Config View Patient Trends menu.
Config Settings
Mini trends...
View vitals every/View vitals for
It opens the Mini trends menu which has go to main menu as its first menu
choice.
Factory Default
1 min/40 min

View vitals every is displayed when Display as in View patient trends is
numbers. It allows the user to choose the set of viewable times for which to
display data. View vitals for is displayed when Display as in View patient
trends is graphs. It allows the user to choose the span of time to be viewed.
Default Table Name
Adult
Pediatric
Neonate
Revision C
Revision C
PACE OFF
yes
N/A
It allows the user to instruct the Monitor to analyze ECG data for pacemaker
pulse
User specifies whether the monitor will detect and display arrhythmia
conditions
It allows the user to instruct the Monitor to "learn" a new ECG pattern so that it
can more accurately calculate the patients heart rate
Pacer detection?
Arrhythmia detection
Re-learn
N/A
0.5 to 40 Hz
N/A
crisis
procedural
procedural
User specifies the default sweep speed for all cardiac-based waveforms
(except the ECG waveform if Fixed ECG sweep speed? is yes). This choice
appears in all menus associated with cardiac-based waveforms. A change in
one menu affects all cardiac-based waveforms.
The user chooses this to interject one cycle of a 1 mV square-wave into the
display of the ECG waveform
User specifies the type of display filtering done on raw ECG waveform data
before it is displayed or recorded.
User specifies the size of QRS width detection by the EKPro algorithm.
User specifies audio alarm associated with these alarms.
User specifies the audio alarm associated with ECG VTACH in Adult and
Pediatric modes. Menu item is not viewable in Neonate mode.
User specifies the audio alarm associated with ECG LEAD FAIL.
User specifies the audio alarm associated with ECG REPLACE
ELECTRODES.
User specifies the audio alarm associated with ECG ARTIFACT.
User specifies the color for information displayed in ECGs waveform area.
It opens the Config ECG menu.
Cardiac sweep speed
calibration pulse
Display filter
QRS width
other alarm priorities
VTACH
Lead fail
Replace electrodes
Artifact

2042481-001
Select ECG's color
Config settings...
N/A
green
message
Normal
25.0 mm/s
It opens the Advanced ECG menu.
N/A
1X
User specifies the multiplying factor used to change the appearance of the
ECG waveforms displayed.
Waveform size
Lead II
Factory Default
User can choose the lead to be displayed as the ECG waveform.
Lead selection
Setup ECG
Default Table Name
Adult
Pediatric
Neonate
C-7
C-8

2042481-001

lo
diastolic hi
lo
mean hi
lo
It opens the Advanced NIBP menu.
Adjust limits
systolic hi
User specifies the interval of time between auto mode determinations.
User specifies the number of determinations to be done at 4th BP series

interval.
User specifies the auto mode interval for step 4 of the protocol.
User specifies the number of determinations to be done at 3rd BP series

interval.
User specifies the number of determinations to be done at 2nd BP series

interval.
User specifies the number of determinations to be done at 1st BP series

interval.
Auto BP
repeat
4nd BP Series
repeat
3nd BP Series
repeat
2nd BP Series
repeat
1st BP Series
N/A
A=40, P=40
A=140, P=100
A=30, P=30
A=120, P=90
A=80, P=70
A=200, P=150
auto-set
manual
x1
q60min
x2
q30min
x4
q15min
x4
q5min
N/A
no
When yes, the speed of the ECG waveform is fixed at 25.0 mm/s. When no,
the speed of the ECG waveform changes according to the Cardiac sweep
speed menu choice.
An extended menu where the user may configure a custom auto mode
protocol.
Factory Default
setup custom series
Setup NIBP
Fixed ECG sweep speed?
Default Table Name
Adult
Pediatric
Neonate
Revision C
Revision C
User specifies the audio alarm associated with NIBP OVERPRESSURE.
User specifies the audio alarm associated with NIBP PUMP TIMEOUT.
User specifies the audio alarm associated with NIBP TOTAL TIMEOUT.
Overpressure
Pump timeout
Total timeout
no
yes
yes
25.0 mm/s
warning
It opens the Advanced SpO2 menu.

It allows the user the option of viewing the graphic signal strength bar.
Controls how the Monitor behaves concerning the handling of SpO2 derived
pulse rate.
Allows use to specify monitor behavior when the SpO2 LOST PULSE or SpO2
SENSOR OFF alarm is issued.
User specifies whether C-LOCK is enabled.
User specifies the sweep speed for all cardiac waveforms. This choice appears
in all menus associated with cardiac waveforms. A change in one menu
affects all cardiac waveforms.
User specifies audio alarm associated with limit alarms, including SpO2 PR
limit alarms if View SpO2 PR? is set to yes.
View signal strength bar?
View SpO2 PR?
Enable Spot check?
Turn c-Lock on?(NELLCOR ONLY)

2042481-001
Cardiac sweep speed
no
N/A
hi 100 A = lo 90, P = lo
92
Adjust limits
yes
purple
It allows the user the option of viewing the SpO2 waveform area.
User specifies the color for information displayed in NIBPs vital sign area as
well as information related to NIBP that is displayed in the Limit and Full and
Mini trends windows.
procedural
procedural
procedural
procedural
procedural
N/A
warning
auto
Factory Default
View waveform?
Setup SpO2
Select NIBP's color
User specifies the audio alarm associated with NIBP LEVEL TIMEOUT.
User specifies the audio alarm associated with NIBP NO DETERMINATION.
No determination
Level timeout
User specifies whether the limit alarms associated with NIBP are issued as
either warning or crisis alarms.
User specifies the pressure the Monitor initially pumps to for the next
determination.
Initial target pressure
Default Table Name
Adult
Pediatric
Neonate
C-9
C-10

2042481-001
N/A
12
Normal
OFF
Normal
OFF
User specifies the audio alarm associated with SpO2 SENSOR FAULTY.
User specifies the audio alarm associted with SpO2 SENSOR OFF.
User specifies the audio alarm associated with SpO2 SIGNAL QUALITY
User specifies the color for the information displayed in SpO2s vital sign and
waveform areas as well as information related to SpO2 that is displayed in the
Limit and Full and Mini trends windows.
It opens the Config SpO2 menu.
User specifies the averaging time used by the Masimo SpO2 algorithm to
calculate SpO2 values
User specifies the sensitivity thresholds used by the Masimo SpO2 algorithm
for calculating SpO2 values under low perfusion conditions
User specifies the whether or not the Masimo SpO2 algorithm calculates the
SpO2 values quicker
User specifies the setting for the Nellcor SpO2 algorithm for rejecting noise
and calculating SpO2 values.
User specifies the time setting for the Nellcor SpO2 algorithm to holf off limit
alarms or OFF to disable any hold off.
Sensor faulty
Sensor off
Singal quality (MASIMO ONLY)
Select SpO2's color
Config settings...
Averaging (MASIMO ONLY)
Sensitivity (MASIMO ONLY)
FAST SAT (MASIMO ONLY)
Response mode (NELLCOR ONLY)
SAT SECONDS (NELLCOR ONLY)
lo
Adjust limits
User specifies the multiplying factor used to change the appearance of the
RESP waveform.
Waveform size
hi
1X
It allows the user the option of viewing the RESP waveform area.
View waveform?
A=6, P=10
A=30, P=60
N/A
yes
User can choose the lead from which the respiration waveform is characterized
and the impedance respiration rate is derived.
Lead II
blue
message
procedural
Lead to analyze
Setup RESP
procedural
User specifies the audio alarm associated with SpO2 SENSOR

DISCONNECTED.
Sensor disconnected
procedural
procedural
User specifies the audio alarm associated with SpO2 LOST PULSE.
Lost pulse
N/A
Factory Default
Default Table Name
Adult
Pediatric
Neonate
Revision C
Revision C

2042481-001
User specifies the audio alarm associated with TEMP TOO HOT
User specifies the audio alarm associated with TEMP DISCONNECTED
Disconnected
User specifies audio alarm associated with these alarms
Too Hot
It opens the Advanced TEMP menu
User specifies the audio alarm associated with TEMP BAD PROBE
User specifies temperatures mode of operation
Choose mode
Bad Probe
User specifies the unit of measure used to display temperature readings
User specifies whether auto-switching Resp parameter is or is not active.
It opens the Config RESP menu.
Unit of measure
Setup TEMP
Turn on RESP with ECG?
Config settings...
User specifies the color for information displayed in RESPs waveform and vital
sign areas as well as information related to RESP that appears in the Limit and
Full and Mini trends windows.
User specifies the audio alarm associated with RESP ARTIFACT.
Artifact
Select RESP's color
procedural
User specifies the audio alarm associated with RESP BASELINE

SATURATION.
Saturation
procedural
procedural
procedural
N/A
N/A
predictive
A=no; P=yes
N/A
blue
procedural
procedural
warning
N/A
User specifies the audio alarm associated with RESP LEAD FAIL.
warning
Lead fail
User specifies audio alarm associated with limit alarms.
auto
The user specifies the alarm type associated with RESP RATE
APPROACHING HR.
It allows the user to select the type of filtering performed.
Cardiogenic filter
A/P=12.5mm/s
N/A
Factory Default
Resp approaching
User specifies the sweep speed for all respiratory waveforms. This choice
appears in all menus associated with respiratory waveforms. A change in one
menu affects all respiratory waveforms.
It opens the Advanced RESP menu.
Resp sweep speed
Default Table Name
Adult
Pediatric
Neonate
C-11
C-12
yellow
N/A
no
User specifies the color for information displayed in TEMPs vital sign area as
well as information related to TEMP that is displayed in the Limit and Full and
Mini trends windows
It opens the Config TEMP menu
User specifies whether the units used to display the temperature must always
fixed on C
Select TEMP's color
Config settings...
Allow C units only?

2042481-001
Allows the user to access continuous options.
setup continuous
save default changes
Other System Settings
Delayed memory (in seconds)
setup timed
It allows the user to copy the contents of the active table onto the confirmed
user default table.
Delayed memory in seconds.
Allows the user to access timed options.
Length of Alarm trace.
It opens the Config RECORDER menu.
Config settings...
Length of strip (in seconds)
It allows the user to specify the location of printouts that result from pressing
the record .
Record key printout
Delayed memory in seconds.
Length of Timed recording.
Length of strip (in seconds)
Delayed memory (in seconds)
It allows the user to choose the tracing speed of a Timed recording.
Allows the user to access timed options.
Chart speed
setup timed
N/A
N/A
20
N/A
N/A
at bedside
25.0 mm/s
N/A
N/A
OFF
User specifies whether an auto printout of Vitals Summary is initiated at the

end of an NIBP/TEMP determination.
Auto printout of vitals summary?

Allows the user to access continuous options.
no
User specifies whether or not a Vitals Summary block of info is printed at the
beginning of real time printouts.
Vitals summary with printout?
setup continuous
no
User specifies whether the detection of patient-type warning or crisis alarm

generates an Alarm print.
Print on alarm?
Setup RECORDER
Factory Default
Default Table Name
Adult
Pediatric
Neonate
Revision C
Revision C
mm/dd/yy
military
English
yes
yes
no
no
OK
User specifies the format the date appears on the screen and on all recordings.
User specifies how time is to be formatted when it appears on the display and
all recordings. For all languages, when am/pm is confirmed, the time is
displayed as HH:MM am or HH:MM pm.
The user specifies the language to be used for text that appears throughout
the Monitors user interface. The language choice is active for all patient
settings tables. The new language becomes effective upon selection but is not
copied onto the active table until save default changes has been confirmed.
The language confirmed has no influence on service mode which is always in
English.
The user specifies whether the unit of measure for all parameters is displayed
in each parameters respective vital sign area.
The user specifies whether alarms limits for all parameters are displayed in
each parameters respective vital sign area.
The user specifies whether pressure values are displayed in kPa is in addition
to being displayed in mmHg.
When selected, the user is prompted with a yes/no dialog box with the text
CAUTION! This will reset ALL defaults! Are you sure you want to do this?
It allows the user to transmit the contents of all six tables either to another
Monitor or PC.
reset ALL to factory
send ALL defaults
Select time format
Language
Display units?
Display limits?
Display kPa values?
N/A
full color
Select date format
It opens the Config Other System Settings menu.
User specifies the volume of the overall system.
Adjust system volume
Config settings...
User specifies the volume of the sounds as listed in USER INTERFACE

OVERVIEW.
It opens the Advanced Other System Settings menu.
Advanced Settings...
Adjust keyclick volume
N/A
An extended menu where the user specifies a new date and time by manually
adjusting the month, day, year, hour, minute and second
adjust date & time
User specifies Monitor color configuration.
no
User controls when battery icon is viewable when monitor in not on battery
power.
Always display battery icon?
Select color format
no
When selected, the user is prompted with a yes/no dialog box with the text
CAUTION! This will exit configuration mode. All unsaved changes will be lost.
Are you sure you want to do this?
exit config mode
N/A
Factory Default
Default Table Name
Adult
Pediatric
Neonate

2042481-001
C-13
C-14
User specifies serial data transfer for this port.
Baud rate
Allows user to configure serial 2 port settings.

User specifies the protocol of this port on monitor power-up.
Serial 2 setup
User specifies serial data transfer for this port.
User specifies the protocol of this port on monitor power-up.
Allows user to configure serial 1 port settings.
Startup mode
Baud rate
Startup mode
Serial 1 setup
User specifies which port, if any, is enabled for remote access.
Remote access
User specifies address for network module communication.

It allows the user to specify the waveforms to be sent when a serial port is
communicating via the MPS binary protocol.
IP address
It allows the user to specify the host communications address for this particular
monitor.
Waveforms to send
Unit address
Config HostComm...
Default Table Name
9600
ASCII cmd
N/A
(Viewable only in
operation
mode)38400
ASCII cmd
NA
None
2 chosen
0.0.0.0
Factory Default
Adult
Pediatric
Neonate

2042481-001
Revision C
D-1
Auxiliary Output

2042481-001
Revision C
For your notes
D-2

2042481-001
Revision C
Auxiliary Output:
Auxiliary Output
The auxiliary output is a nonisolated signal input/output meant only for
connection to another medical device that is compliant with IEC 601-1.
Connection to a noncompliant device could result in a safety risk by exceeding
current limits.
The auxiliary output connector provides an analog ECG waveform output. The
analog ECG waveform signal is a high level (1 V/mV) representation of the
primary lead. The connector is a two-conductor 3.5 mm stereo jack that mates
with a 3.5 mm stereo plug (Shogyo SPY 1011, Shogyo SPY 1012, or equivalent).
Cable construction should be shielded, three conductor with PVC insulation or
equivalent insulating material.
Pin Out:
Tip
No Connection
Ring
ECG Analog Output
Sleeve
Signal Return
Dynamic range
> 4.75 V minimum
Scale Factor*
1 V/mV 5%
Output Impedance/Short Circuit

Protection
<100
Frequency Response
0.05 Hz - 100 Hz +1/-6 dB
Delay**
22 5ms
* Maximum load of 50 k necessary to maintain scale factor.

** Internal pacemaker pulses are not represented in the auxiliary output.
Revision C

2042481-001
D-3
Auxiliary Output:
D-4

2042481-001
Revision C
Revision C
EMC Compliance

2042481-001
E-1
For your notes
E-2

2042481-001
Revision C
EMC Compliance: Electromagnetic Compatibility (EMC)
Electromagnetic Compatibility (EMC)

Changes or modifications to this system not expressly approved by GE Medical
Systems can cause EMC issues with this or other equipment. This system is
designed and tested to comply with applicable regulation regarding EMC and
must be installed and put into service according to the EMC information stated
in this appendix.
WARNING
Use of portable phones or other radio frequency (RF) emitting
equipment near the system may cause unexpected or adverse
operation.
WARNING
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.
Guidance and Manufacturers Declaration Electromagnetic Emissions

The Dash 2500 Patient Monitor Service Manual is intended for use in the
electromagnetic environment specified below. It is the responsibility of the
customer or user to assure that the Dash 2500 Patient Monitor Service Manual is
used in such an environment.
Emissions Test
Compliance
RF Emissions
EN 55011
Group 1
RF Emissions
EN 55011
Class A
Harmonic Emissions
EN 61000-3-2
Class A
Voltage Fluctuations/
Flicker Emissions
EN 61000-3-3
Complies
Revision C
Electromagnetic Environment Guidance

The equipment uses RF energy only for its internal function.
Therefore, its RF emissions are very low and are not likely to cause
any interference in nearby electronic equipment.
The equipment is suitable for use in all establishments other than

domestic and those directly connected to the public low-voltage
power supply network that supplies buildings used for domestic
purposes.

2042481-001
E-3
Guidance and Manufacturers Declaration Electromagnetic Immunity

Immunity Test
Electrostatic
Discharge (ESD)
EN 61000-4-2
EN 60601 Test Level
Compliance Level
6 kV contact
6 kV contact
8 kV air
8 kV air
Floors should be wood, concrete or ceramic

tile. If floors are covered with synthetic
material, the relative humidity should be at
least 30%.
Electrical Fast
Transient/Burst
EN 61000-4-4
2 kV for power supply

lines
2 kV for power
supply lines
Mains power should be that of a typical

commercial or hospital environment.
1 kV for input/output
lines
1 kV for input/
output lines
Surge
EN 61000-4-5
1 kV differential mode
1 kV differential
mode
2 kV common mode
2 kV common
mode
< 5% Ut (> 95% dip in Ut)

for 0.5 cycles
< 5% Ut (> 95% dip in

Ut) for 0.5 cycles
< 40% Ut (> 60% dip in Ut)

for 5 cycles
< 40% Ut (> 60% dip

in Ut) for 5 cycles
< 70% Ut (> 30% dip in Ut)

for 25 cycles
< 70% Ut (> 30% dip

in Ut) for 25 cycles
< 5% Ut (> 95% dip in Ut)

for 5 s
< 5% Ut (> 95% dip in

Ut) for 5 s
3 A/m
3 A/m
Voltage dips,
short
interruptions
and voltage
variations on
power supply
input lines
EN 61000-4-11
Power
Frequency (50/
60 Hz) Magnetic
Field
EN 61000-4-8

commercial or hospital environment.

commercial or hospital environment. If the
user of the equipment requires continued
operation during power mains interruptions,
it is recommended that the equipment be
powered from an uninterruptible power
supply or a battery.
Power frequency magnetic fields should be at

levels characteristic of a typical location in a
typical commercial or hospital environment.
NOTE:
Ut is the AC mains voltage prior to application of the test level.
E-4

2042481-001
Revision C
Guidance and Manufacturers Declaration Electromagnetic Immunity

Immunity Test
EN 60601 Test Level
Compliance
Level

Portable and mobile RF communications equipment
should not be used closer to any part of the
equipment, including cables, than the recommended
separation distance calculated from the equation
applicable to the frequency of the transmitter.
Recommended separation distance
Conducted RF
EN 61000-4-6
3 Vrms
150 KHz to 80 MHz
3 V rms
Radiated RF
EN 61000-4-3
3 V/m
80 MHz to 2.5 GHz
3 V/m
d = 1.2
d = 1.2
P 80 MHz to 800 MHz
d = 2.3
P 800 MHz to 2.5 GHz
Where P is the maximum output power rating of the

transmitter in watts (W) according to the transmitter
manufacturer, and d is the recommended separation
distance in meters (m).
Field strengths from fixed RF transmitters, as
determined by an electromagnetic site surveya,
should be less than the compliance level in each
frequency rangeb.
Interference may occur in the vicinity of equipment
marked with the following symbol:
Note 1: At 80 MHz and 800 MHz, the higher frequency range applies.
Note 2: These guidelines may not apply in all situations. Electromagnetic propagation is affected by reflection from
structures, objects, and people.
a
Field strengths from fixed transmitters, such as base stations for radio (cellular/cordless) telephones and land
mobile radio, AM and FM radio broadcast, and TV broadcast cannot be predicted theoretically with
accuracy. To assess the electromagnetic environment due to fixed RF transmitters, an electromagnetic site
survey should be considered. If the measured field strength in the location in which the equipment is used
exceeds the applicable RF compliance level above, the equipment should be observed to verify normal
operation. If abnormal performance is observed, additional measures may be necessary, such as reorienting or relocating the equipment.
b
Over the frequency range 150 KHz to 80 MHz, field strengths should be less than 3 V/m.
Revision C

2042481-001
E-5
Recommended Separation Distances

The table below provides the recommended separation distances (in meters)
between portable and mobile RF communications equipment and the Dash
2500 Patient Monitor Service Manual.
electromagnetic environment on which radiated RF disturbances are controlled.
The customer or the user of the Dash 2500 Patient Monitor Service Manual can
help prevent electromagnetic interference by maintaining a minimum distance
between portable and mobile RF communications equipment (transmitters) and
the Dash 2500 Patient Monitor Service Manual as recommended below,
according to the maximum output power of the communications equipment.
Separation Distance in Meters (m) According to Frequency of Transmitter
Rated Maximum Output
Power of Transmitter in
Watts
150 kHz to 80 MHz a
0.01
0.12
0.12
0.23
0.1
0.38
0.38
0.73
1.2
1.2
2.3
10
3.8
3.8
7.3
100
12
12
23
d = 1.2
80 MHz to 800 MHz a

d = 1.2
800 MHz to 2.5 GHz a
d = 2.3
At 80 MHz and 800 MHz, the separation distance for the higher frequency range applies.
For transmitters rated at a maximum output power not listed above, the
recommended separation distance [d] in meters (m) can be estimated using the
equitation applicable to the frequency of the transmitter, where P is the
maximum output power rating of the transmitter in watts (W) according to the
transmitter manufacturer.
NOTE:
These guidelines may not apply in all instances. Electromagnetic
propagation is affected by absorption and reflection from structures,
objects and people.
E-6

2042481-001
Revision C
Compliant Cables and Accessories

WARNING
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.
The table below lists cables, transducers, and other applicable accessories with
which GE Medical Systems claims EMC compliance.
NOTEAny supplied accessories that do not affect EMC compliance are not
included.
Part No
Revision C
Description
Maximum Lengths
2021141-001
CABLE ASSY ECG 3 LEAD W/GRAB, AHA
2022948-001
CABLE ASSY 3/5 LEAD ESU MULTLNK ECG, AHA
2017003-001
CABLE ASSY ECG MLT-LNK 3/5 LEAD, AHA
3.6M
2017004-001
CABLE ASSY ECG 3 LEAD NEO, AHA
3.6M
900716-001
900716-001 Leadwire Set, ECG, Multi-Link, Mini-Clip/

DIN, Neo, AHA, 3/set
24 in.
002200
002200 Cuff, NIBP, Dura-Cuf, Inf, 2 TB, Org, Submin, 5/

bx
002201
002201 Cuff, NIBP, Dura-Cuf, Chd, 2 TB, Grn, Submin, 5/

bx
002202
002202 Cuff, NIBP, Dura-Cuf, Sm Ad, 2 TB, Royal Blu,

Submin, 5/bx
002203
002203 Cuff, NIBP, Dura-Cuf, Ad, 2 TB, Navy, Submin, 5/

bx
2017002-003
CABLE ASSY SPO2 MASIMO
2002800-001
2002800-001 Sensor, SPO2, Masimo, Finger, Ad,

Reusable
2021406-001
2021406-001 CABLE ASSY SPO2 NELLCOR OXIMAX
70124021
SPO2- SENSOR DS 100A
2008774-001
SENSOR TURBO TEMP LONG, WHITE CORD
2008775-001
SENSOR TURBO TEMP LONG RECTAL,WHITE CORD
615118
Probe Covers 20/box

2042481-001
2.4M
3M
E-7

For your notes
E-8

2042481-001
Revision C
Revision C
Connection

2042481-001
F-1
Connection:
For your notes
F-2

2042481-001
Revision C
Technical Specifications
Environmental Specifications
Item
Description
Operational
Temperature
5 C to 40 C (41 F to 104 F)
Operating
Atmospheric
700 to 1060 hPa
Storage
Transportation/
Atmospheric Pressure
500 to 1060 hPa
Storage Temperature
-40 C to 70 C (-6 F to 158 F)
Humidity Range
0% to 95% non-condensing
Radio Frequency
Complies IEC Publication 601-0-2 (April 1993) Medical Electrical

Equipment Electromagnetic Compatibility Requirements and
Tests, and CISPR II (Group 1, Class A) for radiated and conducted
emissions
IPX 0
This device is not protected against the ingress of liquids
Product Compatibility
CAUTIONS
Do not use the unit with any monitor except the Dash 2500 Monitor
Specified.
Contact your sales representative before connecting the network
module to your network to verify compatibility.

Do not insert metallic objects, inflammables, water or other fluids into
the unit.
There are no user-serviceable parts within this device.
Revision C
When printing ECG from a Unity device, the filter setting will always be .05120 Hz, regardless of the filter setting on the Monitor.

2042481-001
F-3
Connection: External Connectors
External Connectors
The following tables provide pin-by-pin descriptions and signal names for the
external connectors.
Ethernet Port
This RJ-45 connector connects the network module to the monitoring network.
8-Pin Ethernet Connector
F-4
Pin
Name
Input/Output
Description
LAN_TRANSMIT+
Network transmit non-inverted differential

output.
LAN_TRANSMIT
Network transmit inverted differential

output.
LAN_RECEIVE+
Network receive non-inverted differential

input.
NC
NC
LAN_RECEIVE
Network receive inverted differential input.
NC
NC

2042481-001
Revision C
Service Port
The RS-232 connector is provided as one asynchronous port for software
downloading.
8-Pin RJ-45 Connector
Pin
Revision C
Name
Input/Output
HC_232_TX
HC_232_RX
NC
COMMON
SP_232_TX
NC
SP_232_RX
NC
Description
Signal Common
O

2042481-001
F-5
Connection: External Connectors
LEDs
System Status LED Chart
LED State
F-6
Function
Description
Green ON Solid
Working
Communications with network is

functioning properly.
Yellow ON solid
Pending
Communications with network is

pending.
Yellow blinking 3 times fast in 1

second increments, off for 1
second
Duplicate
address
Another device on the monitoring

network is broadcasting RWHAT
packets using the same location as
this unit.
Green, slowly blinking

(once every 2 seconds)
Boot Code
Boot code is running.
Alternating blinking: Green/Yellow

fast. Alternating bi-color LED
predominantly Yellow - initial
download.
Green - completion
Downloading
The unit is being downloaded, either

automatically or manually.
Yellow slowly blinking

Communicatio
ns error
Connected to network, but cannot

communicate with the Dash 2500
Monitor.
Yellow blinking fast

(twice every second)
Other errors
Network module is malfunctioning.

Network module is not compatible
with software in the Dash 2500
Monitor.

2042481-001
Revision C
Communication Adaptor Connector

This connector is reserved for connection to GE Medical Systems Information
Technologies network module ONLY.
Pin Number
Revision C
Function
Ground
Fused +5 volts
Fused +12 volts
No Connection
Ground
Remote Alarm
No Connection
10
No Connection
11
12
Port Enable Control
13
14
No Connection
15
No Connection

2042481-001
F-7
Connection: Cleaning
Cleaning
Wipe the exterior of the module with a cloth slightly dampened with mild
detergent. Wipe with a 10% solution of household bleach, Amphyl (reg.
trademark of Sterling Winthrop, Inc.) a green soap and water solution, or
Cidex (reg trademark of Johnson & Johnson).
Do not immerse the module.
Do not clean the module with isopropyl alcohol or other solvents, except
when preparing for mounting adhesives.
Do not sterilize the module in an autoclave.
Installation Configuration Procedure

This procedure describes how to initially configure the network module to your
Dash 2500 Monitor and Unity Network. These procedures are intended to be
performed by service personnel or biomedical engineers.
NOTE: Do not install the Dash 2500 monitor into the GE Unity network with
more than 1000 Unity devices.
Preparation
Special Equipment
This procedure requires the installer to have the following:
RJ-45 Cable P/N 418335-00X
Clinical network (Unity Network)
CIC version 3.0.2 or later
Installation of the network module
F-8
1.
Turn off the power at the Dash 2500 Monitor.
2.
Remove the Interface cover on the rear of the Dash 2500 Monitor.
3.
Connect the module to the 15-pin connector and insert the supplied screw
through the module. Fasten securely.
4.
Replace the Interface cover.

2042481-001
Revision C
Network module Setup

Connect monitor to network:
1.
Turn off the power at the Dash 2500 Monitor.
2.
Connect network cable to the port labeled as Ethernet on the rear of the
Dash 2500 Monitor. Connect the other end of the cable to the clinical
network.
3.
Turn on the power to the Dash 2500 Monitor.
Set up IP address:
The Dash 2500 Monitor is an Ethernet device bounded with an IP address. It
communicates with CIC devices via the clinical network. There are two ways to
set up the IP address:
Default IP address. (If your CIC IP is 126.XXX.YYY.ZZZ, please use this method)
In this method, the Dash 2500 Monitor IP address will be set automatically.
No configuration is needed.
By factory default, the IP address in Dash 2500 Monitor configuration menu
is set as 0.0.0.0. The monitor will automatically generate a default IP
address calculated from its MAC address. This IP address is unique in all GE
Unity devices and follows below formula:
126. XXX. YYY. ZZZ
where the XXX, YYY and ZZZ are the last three numbers of the monitor MAC
address.
NOTE: When using default IP address, the displayed IP 0.0.0.0 showing in

Dash 2500 configuration menu is not the real IP. Customer shall
ignore it.
Specified IP address (If your CIC IP is not 126.XXX.YYY.ZZZ, please use this
method)
In this method, customer shall set the Dash 2500 Monitor IP address
manually.
NOTES
The IP address of the Dash 2500 Monitor must be unique and valid in
the entire clinical network.
The IP address of the Dash 2500 Monitor must be in the same network
address of the intended CIC devices. For example, if the CIC IP address is
172.16.***.*** in a class-B sub-network, the valid IP address range for
monitor is 172.16.0.1~172.16.255.254.
How to set up the specified IP address?

1. Enter the configuration menu (consult Dash 2500 Monitor service
manual Appendix C).
Revision C
2.
Turn and press the Trim Knob to select other system settings.
3.
Turn and press the Trim Knob to select Config HostComm...

2042481-001
F-9
Connection: Installation Configuration Procedure

4. Select IP address sub-menu, select each of the four numeric fields and
set the field values by rotating the Trim Knob. Press the Trim Knob after
adjusting each field value to confirm the setting.
NOTE: Dash 2500 monitor cant inspect the duplicate IP address in the
Unity network. If there are other devices with same IP address in
network, the monitor will still send device identification information
to the CIC. This causes the CIC cant read the IP address normally.
So please make sure Dash 2500 monitor uses the unique IP address
in the network when installation.
5. In the Admit Patient menu, select ADULT and enter the bed and unit
number for this Monitor.
6.
Save default changes.
7.
Repeat step 5 for PEDIATRIC and NEONATE modes.
8.
Exit config mode.
Re-set up
To re-set up type for the network function, enter into boot service menus to clear
config memory. For detail steps, refer to Using the Boot Service Menu.
F-10

2042481-001
Revision C
Boot Service Menus

The boot service menus described in this section are presented for advanced
users and service personnel only. In most cases, access to these menus will not
be necessary and only experienced technicians should attempt to use them.
Preparation
Special Equipment
Computer to act as a terminal with the following minimum requirements:
Windows XP compatible
CD drive
RS232C serial port
PC DIDCA P/N 2006550-001
RJ-45 Cable P/N 418335-00X
GE Medical System Information Technologies UPDATE.EXE program or any

terminal emulation program
Interconnection
To connect a personal computer (PC) to the network module (unit), complete the
following steps in the order given.
1.
Connect the RJ-45 cable to the RJ-45 connector labeled Serial 2 on the unit.
2.
Connect the other end of the RJ-45 cable to PC DIDCA, which is connected
to the 9-pin D-type connector labeled COMMS or COMM 1 at the rear of the
PC.
3.
Connect power cable between the AC connector and the AC power outlet.
PC Setup
Follow the steps in the order listed.
1.
Apply power to the PC and wait for the C:\> prompt.
2.
Go to the directory with the UPDATE.EXE file.

If you are using another terminal emulation program, set the baud to 9600,
8 data bits, 1 stop bit, and no parity, and no flow control.
3.
At your PC, do the following:

Type: update
Press: ENTER key
Select: F7 (TERMINAL EMULATOR menu)
Revision C

2042481-001
F-11
Connection: Boot Service Menus

Select: F3 (for 9600 baud)
4.
While holding down the lowercase b key continuously at the PC, power ON
the Unity Adapter (Dash 2500 Monitor).
Using the Boot Service Menu

The following BOOT SERVICE MENU should appear at the PC. If the file server
selection menu appears first, select service menu.
BOOT SERVICE MENU
1 Change Ethernet Address
2 Change Internet Address
3 Change IPC 1928 ID (9999)
4 Clear Config Memory
5 Country Selection: FRANCE
6 Exit
Your selection -->
Each selection in the BOOT SERVICE MENU is described below. If you enter the
wrong configuration data for any selection, exit the menu, reenter the menu,
and type over the old data.
Select 1: Change Ethernet Address. This selection allows you to change the
Ethernet address of the unit.
Select 2: Change Internet Address. This selection allows you to change the
Internet address of the unit. To generate an Internet address from an
Ethernet address, GE Medical Systems Information Technologies simply
converts the last three bytes of the Ethernet address from hex to decimal.
This combines the unique identifier along with the network ID to produce
the entire Internet address.
NOTE:
This IP address will be overwritten by a valid address from the Dash
2500 Monitor when it is connected.
WARNING
Duplication of an Internet address on the network will cause
lost data. If you change the factory assigned Internet address,
you must first record all other Internet addresses used on your
network to avoid duplication.
F-12

2042481-001
Revision C
Select 3: Change the Network Module ID Number. This selection allows you
to input the unique ID number from the ID number label on the unit. This
number is coded into the software at the factory when the ID number label
is applied. Ensure that the ID number from the label is the same as the
number you input.
New IPC-1928 ID: ___ (range 0 to 9999)(Press ENTER key.)
The IPC-1928 ID has been set to ___.
Revision C
Select 4: Clear Config Memory. This selection allows you to clear the
configurable memory and ID number. The Ethernet and internet addresses
are not affected when you clear the configuration.
Select 5: Country Selection (xxx, xxx is the current country). This selection
selects what country and software the unit is using. The default is English.

2042481-001
F-13
Connection: Service Menus
Service Menus
The service menus described in this section are presented for advanced users
and service personnel only. In most cases, access to these menus will not be
necessary and only experienced technicians should attempt to use them.
Preparation
Special Equipment
Personal computer (PC) with the minimum requirements:
Windows XP compatible
CD drive
RS232C serial port
PC DIDCA P/N 2006550-001
RJ-45 Cable P/N 418335-00X
GE Medical System - Information Technologiess UPDATE.EXE program or

any terminal emulation program.
Interconnection
To access the service menu, complete the following steps in the order given.
1.
Connect the RJ-45 cable to the RJ-45 connector labeled Serial 2 on the unit.
2.
Connect the other end of the RJ-45 cable to PC DIDCA, which is connected
to the 9-pin D-type connector labeled COMMS or COMM 1 at the rear of the
PC.
PC Setup
Follow the steps in the order listed.
1.
Apply power to the PC and wait for the C:\>prompt
2.
Go to the directory with the UPDATE.EXE file.

If you are using another terminal emulation program, set the baud to 9600,
8 data bits, 1 stop bit, no parity, and no flow control.
3.
At your PC, do the following:

Type: update
Press: Enter Key
Select: F7 (TERMINAL EMULATOR menu)
Select: F3 (for 9600 baud)
4.
F-14
Power On the Network Module (unit)

2042481-001
Revision C
NOTE:
No password prompt will appear on screen
Type password: service (all lower case)
Press Enter key
Communication Tips
Use the following controls if you have problems communicating between the
unit and the PC.
If you enter the wrong configuration data, just exit the menu, reenter the
menu, and type over the old data.
If communication is interrupted, power cycle the unit and type: service

<enter>
The network module software is programmed to disconnect communication

with the PC after 5 minutes if no interaction is detected. Because the unit
can be programmed from a local PC connection or from the network, only
one user is allowed to configure the unit at a time.
Using the Service Menu

The following SERVICE MENU choices should appear at the PC.
SERVICE MENU (IPC-1928)
1 Revisions
2 Error Log
3 Event Log
4 Location Menu (X-XXXX) (STANDARD)
5 Unit Type (ADULT)
6 Barometric Pressure 760 mmHg
7 Rwhat Database
8 Set the Time and Date
9. Set Language (current = English)
10. View Parameters
11. Exit
Your selection -->
Select 1: Revisions. This selection lists the revision of the network module
main code.
Select 2: Error Log. This selection lists all errors recorded by the network
module main code, similar to the example below.
1 View Next
Revision C

2042481-001
F-15

2 View Previous
3 Clear Error Log
4 Exit
Enn = the event number
WHEN = date and time
SEVERITY = classification of error
5 = SEVERITY_LOG
6 = SEVERITY_HALT
7 = SEVERITY_RESET
8 = SEVERITY_PLANNED_RESTART
CODE = error code
PROCESS = names process that produced error
SR = status register
PC = program counter
HP = heap counter
USP = user stack pointer
SSP = super stack pointer
Select 3: Event Log. This selection lists all events recorded by the network
module main code, similar to the example below.
Enn
WHEN
EVENT
ID
DATA
DESCRIPTION
0000
01/27/06
13:00:27
Cable Off
0001
01/27/06
13:00:27
Cable Off
0002
01/27/06
13:02:39
30203
Cable On
0003
01/27/06
13:02:46
50106
Cable On
0004
01/27/06
13:02:55
10101
Cable On
1 View Next
2 View Previous
3 Clear Error Log
4 Exit
Enn = the event number
WHEN = date and time1 View Next
WHEN = date and time
F-16

2042481-001
Revision C
EVENT ID = ID number for event

DATA = provides further information about the event
DESCRIPTION = provides description of event
Select 4: Location Menu (X-XXX) (STANDARD). This selection is inaccessible.
Select 5: Unit Type (ADULT). This selection is inaccessible.
Select 6: Barometric Pressure 760 mmHg. This selection is inaccessible.
Select 7: Rwhat Database. This selection allows the user to see all the Rwhat
packets on the network in different formats.
RWHAT SERVICE MENU
1 Display All
2 Display All (Abbreviated)
3 Display for Resource
4 Display for Resource (Abbreviated)
5 Search for String
6 Search for String (Abbreviated)
7 Exit
Select 8: Set the Time and Date. In this version the Time/Data setting
funtion is disabled.
TIME AND DATE SERVICE MENU
13:08:09 27-JAN-2006
Setting of Time/Date has been disabled in this software
version
Revision C
Select 9: Set Language (English). Ensure that the language selection is

correct for your location. The language selection affects alarm broadcast
messages and printed text.
Select 10. View Parameters. This selection allows the user to view the
parameter values in a demonstration mode.

2042481-001
F-17
F-18

2042481-001
Revision C
World Headquarters
European Representative
Asia Headquarters
GE Medical Systems
Information Technologies, Inc.
8200 West Tower Avenue
Milwaukee, WI 53223 USA
Tel:+ 1 414 355 5000
1 800 558 5120 (US only)
Fax:+ 1 414 355 3790
GE Medical Systems
Information Technologies GmbH
Munzinger Strae 3-5
D-79111 Freiburg
Germany
Tel: + 49 761 45 43 - 0
Fax: + 49 761 45 43 - 233
GE Medical Systems
Information Technologies Asia; GE (China) Co., Ltd.
GE China Technology Park
1 Huatuo Road
Shanghai 201203, P.R. China
Tel: + 86 21 3877 7888
Fax: + 86 21 3877 7451
GE Medical Systems Information Technologies, Inc.

8200 West Tower Avenue Milwaukee, WI 53223 USA
GE Medical Systems Information Technologies, a General Electric Company, going to market as

GE Healthcare
www.gehealthcare.com
0459

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Dash 2500 Patient Monitor

Dash 2500 Patient Monitor

Dash 2500 Patient Monitor

Dash 2500 Patient Monitor

Dash 2500 Patient Monitor

Equipment Overview . . . . . . . . . . . . . . . . . . . . . . . . . 2-1

Dash 2500 Patient Monitor Service Manual

Rear Panel Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-3

Dash 2500 Patient Monitor Service Manual

Field Replaceable Units . . . . . . . . . . . . . . . . . . . . . . . 6-1

Remove/Replace Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-16

Technical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . .A-1

Dash 2500 Patient Monitor Service Manual

RESP Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-11

Test Record . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .B-1

Auxiliary Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .D-1

EMC Compliance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .E-1

Dash 2500 Patient Monitor Service Manual

Service Port . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .F-5

Dash 2500 Patient Monitor Service Manual

Dash 2500 Patient Monitor Service Manual

Dash 2500 Patient Monitor Service Manual

For your notes

Dash 2500 Patient Monitor Service Manual

Introduction: Manual Information

Initial release of the manual

Dash 2500 Patient Monitor Service Manual

Introduction: Safety Information

Assembly operations, extensions, readjustments, modifications, or repairs

The electrical installation of the relevant room complies with the

The equipment is used in accordance with the instructions for use.

use of the accessory in the PATIENT VICINITY; and

evidence that the safety certification of the ACCESSORY has been

Dash 2500 Patient Monitor Service Manual

Introduction: Safety Information

Warnings, Cautions, and Notes

Dash 2500 Patient Monitor Service Manual

Introduction: Equipment Symbols

Defibrillator-proof type CF equipment; type CF equipment is specifically

Potential Equalization Terminal: Terminal for providing a connection

Packaging label depicting the transportation and storage atmospheric

Fragile, handle with care

Dash 2500 Patient Monitor Service Manual

Introduction: Equipment Symbols

WASTE OF ELECTRICAL AND ELECTRONIC EQUIPMENT (WEEE): This symbol

Manufacturing Date: This symbol is acompanied by the date of the

Dash 2500 Patient Monitor Service Manual

Introduction: Service Information

Refer equipment servicing to GE-authorized service personnel only.

Any unauthorized attempt to repair equipment under warranty voids that

It is the users responsibility to report the need for service to GE or to one of

Failure on the part of the responsible individual, hospital, or institution using

Regular maintenance, irrespective of usage, is essential to ensure that the

fiscal week manufactured

production sequence number

Dash 2500 Patient Monitor Service Manual

Dash 2500 Patient Monitor Service Manual

For your notes

Dash 2500 Patient Monitor Service Manual