GE Medical Systems Dash 3000, Dash 4000 Service Manual

Dash3000/4000
Patient Monitor
2000966-105 Revision B
g
GE Medical Systems
Information Technologies
gemedicalsystem.com
NOTE: Due to continuing product innovation, specifications in this manual are subject to change without notice.
Listed below are GE Medical Systems Information Technologies’ trademarks. All other trademarks contained
herein are the property of their respective owners. 900 SC, ACCUSKETCH, AccuVision, APEX, AQUA-KNOT, ARCHIVIST, Autoseq, BABY MAC, C Qwik
Connect, CardioServ, CardioSmart, CardioSys, CardioWindow, CASE, CD TELEMETRY, CENTRA, CHART GUARD, CINE 35, CORO, COROLAN, COROMETRICS, Corometrics Sensor Tip, CRG PLUS, DASH, Digistore, Digital DATAQ, E for M, EAGLE, Event-Link, FMS 101B, FMS 111, HELLIGE, IMAGE STORE, INTELLIMOTION, IQA, LASER SXP, MAC, MAC-LAB, MACTRODE, MANAGED USE, MARQUETTE, MARQUETTE MAC, MARQUETTE MEDICAL SYSTEMS, MARQUETTE UNITY NETWORK, MARS, MAX, MEDITEL, MEI, MEI in the circle logo, MEMOPOR T, MEMOPORT C, MINISTORE, MINNOWS, Monarch 8000, MULTI-LINK, MULTISCRIPTOR, MUSE, MUSE CV, Neo-Trak, NEUROSCRIPT, OnlineABG, OXYMONITOR, Pres-R-Cuff, PRESSURE-SCRIBE, QMI, QS, Quantitative Medicine, Quantitative Sentinel, RAC RAMS, RSVP, SAM, SEER, SILVERTRACE, SOLAR, SOLARVIEW, Spectra 400, Spectra-Overview, Spectra-Tel, ST GUARD, TRAM, TRAM-NET, TRAM-RAC, TRAMSCOPE, TRIM KNOB, Trimline, UNION STATION, UNITY logo, UNITY NETWORK, Vari-X, Vari-X Cardiomatic, VariCath, VARIDEX, VAS, and Vision Care Filter are trademarks of GE Medical Systems Information Technologies registered in the United States Patent and Trademark Office.
12SL, 15SL, Access, AccuSpeak, ADVANTAGE, BAM, BODYTRODE, Cardiomatic, CardioSpeak, CD TELEMETRY
Cumulus, Event-Link Nimbus, HI-RES, ICMMS, IMAGE VAULT, IMPACT.wf, INTER-LEAD, IQA, LIFEWATCH, Managed Use, MARQUETTE PRISM, MARQUETTE MMS, MRT, MUSE CardioWindow, NST PRO, NAUTILUS, O
®
-LAN, CENTRALSCOPE, Corolation, EDIC, EK-Pro, Event-Link Cirrus, Event-Link
®
RESPONDER, MENTOR, MicroSmart,
SENSOR, Octanet, OMRS, PHi-Res,
2
Premium, Prism, QUIK CONNECT V, QUICK CONNECT, QT Guard, SMART-PAC, SMARTLOOK, Spiral Lok, Sweetheart, UNITY, Universal, Waterfall, and Walkmom are trademarks of GE Medical Systems Information Technologies.
© GE Medical Systems Information Technologies, 2002. All rights reserved.
T-2 Dash 3000/4000 Patient Monitor Revision B
2000966-105 28 February 2002

CONTENTS

1 INTRODUCTION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1
Manual Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
Revision History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
Manual Purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
Intended Audience . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
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
2 EQUIPMENT OVERVIEW . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-1
Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3
The Monitoring System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
The Patient Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3
Right Side View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-4
Left Side View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-4
Back View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-5
Optional Alarm Light Indicator . . . . . . . . . . . . . . . . . . . . . . . . . . .2-5
User Interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
Flat Panel Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6
Trim Knob Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6
Power Key . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6
Function Keys . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
Optional RAC 2A Module Housing . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8
Optional Dash Port Docking Station . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Optional ICG Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Optional Wireless LAN System . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-9
Access Points . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
Optional Remote Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
Software Packages and Software Options . . . . . . . . . . . . . . . . . . . . . . .2-10
Technical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
Performance Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-11
Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-11
Alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-12
ECG . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
Invasive Blood Pressure (BP) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
Noninvasive Blood Pressure (NBP) . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
GE Pulse Oximetry (SPO2) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-15
Masimo SET SPO2 Module . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-15
Cardiac Output (CO) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-16
Respiration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-16
Revision B Dash 3000/4000 Patient Monitor i
2000966-105
CONTENTS:
Temperature (TEMP) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-17
Carbon Dioxide (CO2) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-17
Analog Output . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-19
Defibrillator Synchronization Pulse . . . . . . . . . . . . . . . . . . . . . . . . . . 2-19
Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-20
Paper Recorder . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-20
RF Wireless LAN . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-20
Environmental Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-21
Physical Specifications . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-21
Certification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-22
Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-22
Electromagnetic Compatibility Compliance (EMC) . . . . . . . . . . 2-22
FCC Compliance Information Statement . . . . . . . . . . . . . . . . . .2-23
3 INSTALLATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-3
Back Panel Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-3
ETHERNET . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-3
RAC 2A Housing Connectors . . . . . . . . . . . . . . . . . . . . . . . . . . .3-3
Remote Control . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-4
Defib Sync . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-4
AC Power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-4
Front Panel Indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-5
AC Power Indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Battery Power Indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-5
Battery Charging/Ready Indicators . . . . . . . . . . . . . . . . . . . . . . . 3-5
Power Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-5
Optional Ethernet Communication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-6
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-6
Twisted Pair . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
Concentrator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
Node . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
Segment and Branch . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-7
Repeater . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
Bridge . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-8
Twisted Pair Cabling (10BaseT) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-8
Symbol PC Card (Wireless LAN) . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-8
4 MAINTENANCE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1
Maintenance Schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Manufacturer Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-3
Visual Inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-4
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-5
Cleaning Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-5
Cleaning the Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-5
Exterior Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Cleaning the Print Head . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-6
Materials Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-6
Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-6
ii Dash 3000/4000 Patient Monitor Revision B
2000966-105
CONTENTS:
Battery Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-7
Charging . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-7
Conditioning the Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-7
Frequency Guidelines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-7
Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-7
Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-7
Replacing the Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-8
Recycling the Batteries . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-8
Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9
General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9
Recommendations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-9
Test Conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-9
Test Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-9
Power Outlet Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
Ground (Earth) Integrity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
Ground Continuity Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-11
Impedance of Protective Earth Connection . . . . . . . . . . . . . . . .4-12
Ground (Earth) Wire Leakage Current Tests . . . . . . . . . . . . . . . . . . 4-13
Enclosure Leakage Current Test . . . . . . . . . . . . . . . . . . . . . . . . . . .4-14
Patient (Source) Leakage Current Test . . . . . . . . . . . . . . . . . . . . . .4-15
Patient (Sink) Leakage Current Test
(Mains Voltage on the Applied Part) . . . . . . . . . . . . . . . . . . . . . . .4-16
Test Completion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-17
Checkout Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-18
Manufacturer Recommended Test Equipment . . . . . . . . . . . . . . . . . 4-18
Monitor Power-up Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-20
ECG Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-21
5 Lead ECG Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-21
12SL and ACI-TIPI ECG Test . . . . . . . . . . . . . . . . . . . . . . . . . . 4-22
Respiration Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-24
Temperature Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-25
Cardiac Output Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-26
Test with Cardiac Output Simulator II . . . . . . . . . . . . . . . . . . . . 4-26
Test with Marq II Simulator . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-27
Invasive Blood Pressure Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-28
BP1 Connector (AR1) Tests . . . . . . . . . . . . . . . . . . . . . . . . . . .4-28
BP2 Connector (PA2) Tests . . . . . . . . . . . . . . . . . . . . . . . . . . .4-29
Pulse Oximetry Tests for GE SPO2 Oximeter . . . . . . . . . . . . . . . . .4-30
Pulse Oximetry Tests for Masimo SET SPO2 . . . . . . . . . . . . . . . . . 4-32
Noninvasive Blood Pressure Tests . . . . . . . . . . . . . . . . . . . . . . . . . 4-34
Analog Output and Defibrillator Synchronization Tests . . . . . . . . . . 4-36
DEFIB Sync Connector: ECG . . . . . . . . . . . . . . . . . . . . . . . . . . 4-36
DEFIB Sync Connector: Arterial BP . . . . . . . . . . . . . . . . . . . . .4-36
DEFIB Sync Connector: Marker Out (Frequency) . . . . . . . . . . .4-37
DEFIB Sync Connector: Marker Out (Pulse Width) . . . . . . . . . .4-37
Battery Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-39
Graph Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-39
Graph Speed Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-39
Display Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-40
Speaker Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-40
Network Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-40
Remote Control Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-40
RF LAN Test (option) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-40
Dash Port Docking Station Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-41
Revision B Dash 3000/4000 Patient Monitor iii
2000966-105
CONTENTS:
Electrical Safety Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-41
Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-41
RAC 2A Module Housing Test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-41
Electrical Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-41
Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-41
Checkout Procedures Completion . . . . . . . . . . . . . . . . . . . . . . . . . . 4-41
PM Form . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-41
Repair Log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .4-42
5 TROUBLESHOOTING . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1
Service Menus . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Boot Loader Service Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Main Menu Service Mode Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
About Service Mode Menu Option Items . . . . . . . . . . . . . . . . . . . 5-5
Service Mode Menu Option Items . . . . . . . . . . . . . . . . . . . . . . . . 5-5
Review Errors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-8
About the Monitor Error Log . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-8
Downloading the Error Log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-8
Accessing the Review Errors Menu Option Item . . . . . . . . . . . . .5-8
Error Log Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9
Error Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9
Severity of the Error . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-9
Battery Alarms and Messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-10
Alarm Conditions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-10
Error Message . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-11
Power Source Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-12
Wall Receptacle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-12
Power Cord and Plug . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-13
Data Acquisition Tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-14
ECG Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-14
ECG Waveforms Display Incorrectly . . . . . . . . . . . . . . . . . . . . .5-15
ECG Waveforms Do Not Display At All . . . . . . . . . . . . . . . . . . .5-15
Lead Fail Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-15
Pace Detect Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-16
Pace Detect Functions Do Not Work Properly . . . . . . . . . . . . . .5-16
Invasive Blood Pressure Functions . . . . . . . . . . . . . . . . . . . . . . . . .5-17
Setup BP1 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-17
Setup BP2 . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-17
Zero-Reference Both BP’s . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-17
Generate Dynamic BP Waveforms . . . . . . . . . . . . . . . . . . . . . . 5-17
Verify Dynamic BP Results . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-17
Generate Static BP Waveforms . . . . . . . . . . . . . . . . . . . . . . . . . 5-18
BP Waveforms Do Not Appear Correctly On The Display . . . . . 5-18
BP Waveforms Do Not Appear On The Display At All . . . . . . . .5-18
Respiration Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-19
No Respiration Waveform or Rate Appear on the Display . . . . 5-19
Respiration Functions Work Properly on Patient Simulator but not on
Actual Patient . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-20
Noninvasive Blood Pressure Functions . . . . . . . . . . . . . . . . . . . . . . 5-21
NBP Alarms Occur Continuously . . . . . . . . . . . . . . . . . . . . . . . . 5-21
Wireless LAN Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-22
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Service Tips . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-24
Fault/Symptom Analysis . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-24
Acquisition PCB Symptoms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-26
Processor PCB Symptoms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-26
Error Messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-27
Language-Specific Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-29
French Language Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-29
Hungarian, Polish, and Russian, Language Information . . . . . . . . .5-29
Chinese and Japanese Language Information . . . . . . . . . . . . . . . . . 5-29
6 CONFIGURATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-1
Configuring a Monitor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-3
General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-3
Main Menu Selections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5
Set Unit Name . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-5
Set Bed Number . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-5
Patient-Monitor Type . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-6
Set Graph Locations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-6
Communication Confirmation . . . . . . . . . . . . . . . . . . . . . . . . . . .6-7
Problems? . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-7
Admit Menu . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-8
Boot Code Selections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-9
Set Defib Sync Voltage and Pulse Width . . . . . . . . . . . . . . . . . . .6-9
Set Line Frequency . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-9
Set CIC and QS Protocol . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-9
Set MUSE Protocol . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-9
Transcutaneous Pace Blank Length . . . . . . . . . . . . . . . . . . . . . 6-10
Set Country Selection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Wireless LAN . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Set Language . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-11
Completion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-11
Advanced User Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12
Procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-12
Set Time and Date . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12
Transfer Monitor Defaults . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-13
Change Ethernet Address . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-16
Review Errors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-16
Transferring Error Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-19
General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-19
Access the COPY LOGS Menu . . . . . . . . . . . . . . . . . . . . . . . . . 6-20
Select the Monitoring Device . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-20
Select the Error Log Date . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-20
Copy Error Logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-21
Eject Floppy . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-21
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7 CALIBRATION . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-1
Hardware Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3
NBP, Analog Output ECG, Analog Output BP, and End-tidal CO2
Software Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-4
NBP Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
In General . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
Required Test Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
Calibration Procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-5
ECG or BP Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-7
Before you Begin . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-7
ECG Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-7
BP Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-8
End-tidal CO2 Calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-8
8 FIELD REPLACEABLE UNITS AND UPGRADES . . . . . . . . . . . . . . . . . . 8-1
Disassembly Guidelines . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3
Tools Required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-3
Before Disassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-3
Hardware Assemblies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3
PCB Assemblies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-4
Electrostatic Discharge (ESD) Precautions . . . . . . . . . . . . . . . . . 8-4
After Reassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-5
Handle Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-7
Removing the Handle Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-7
Replacing or Upgrading the Dash 3000 Alarm Light Option . . . . . . .8-8
Display Assembly Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
Removing the Display Assembly from the Main Unit . . . . . . . . . . . . . 8-9
Replacing the Backlight Inverter PCB . . . . . . . . . . . . . . . . . . . . . . .8-13
Replacing the Key Pad Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . 8-14
Replacing the LCD Color Display . . . . . . . . . . . . . . . . . . . . . . . . . . .8-15
Replacing or Upgrading the Dash 4000 Alarm Light Option . . . . . .8-16
Replacing the Dash 4000 Front Panel PCB . . . . . . . . . . . . . . . . . . .8-17
. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-17
Main Unit Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-18
DAS and NBP Assemblies . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-18
Main and/or Power Supply Assemblies, Speaker or RF LAN
Upgrade . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-21
Processor/Power Management PCB and Battery Assembly . . . . . .8-22
Power Supply Assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-24
Speaker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-25
RF LAN Upgrade Instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-26
Verify the Wireless LAN ID Number . . . . . . . . . . . . . . . . . . . . .8-35
Verify Wireless LAN Communications . . . . . . . . . . . . . . . . . . . .8-35
Optional DDW Writer Replacement/Upgrade . . . . . . . . . . . . . . . . . . . . .8-36
Replacement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-36
Upgrade . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-36
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CONTENTS:
9 ASSEMBLY DRAWINGS . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-1
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-3
Theory Of Operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-4
Components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-4
Overall Monitor Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-4
Power Supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-5
Data Acquisition System (DAS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-5
DAS Block Diagram with GE SPO2 . . . . . . . . . . . . . . . . . . . . . . 9-6
Processor/Power Management Subsystem . . . . . . . . . . . . . . . . . . . 9-12
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-12
Block Diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-13
Main Microcontroller . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-14
System Control Logic . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-15
Memory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-15
Real-Time Clock . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-15
Audio Subsystem . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-15
Video Subsystem . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-15
Defib Sync . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-16
Optional Thermal Printer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-16
Optional Alarm Light Indicator . . . . . . . . . . . . . . . . . . . . . . . . . .9-16
PC Card . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-16
Peripheral Expansion Interface . . . . . . . . . . . . . . . . . . . . . . . . .9-16
Optional Unity Network Communication . . . . . . . . . . . . . . . . . . 9-17
Ethernet Priority . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-17
Async Communication . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-17
Debug Monitor and Diagnostic LEDs . . . . . . . . . . . . . . . . . . . . . 9-17
Battery Subsystem . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-18
Optional Thermal Printer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-18
Speaker . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-18
Handle Subassembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-18
Interfaces . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-19
Ethernet . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-19
AUX . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-19
Defib Sync . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-19
Peripheral Expansion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-19
Setup and Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-19
Program Code Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-19
Monitor Settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-19
Patient Data Storage . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-19
Time and Date . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-19
Error Log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-20
Electrical Diagram, PN 2004323, Revision D . . . . . . . . . . . . . . . . . . . . . 9-21
Dash 3000/4000 Assembly, PN 2004323, Revision D . . . . . . . . . . . . . .9-22
Part List, PN 419031-003, Rev. C . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-27
Dash 4000 Display Assembly, PN 2004272-001, Rev. C . . . . . . . . . . . . 9-28
Parts List, PN 2004272-001, Rev. C . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-29
Dash 3000/4000 Back, PN 2001875, Revision D . . . . . . . . . . . . . . . . . . 9-30
Parts List , PN 2001875, Rev. D . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-31
Field Replaceable Units (FRU’s) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-32
Dash 3000 FRUs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-32
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CONTENTS:
Dash 4000 FRUs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-32
Port Connections . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-34
Invasive Blood Pressure Cable Connector . . . . . . . . . . . . . . . . . . . . 9-34
GE Pulse Oximetry (SpO2) Cable Connector . . . . . . . . . . . . . . . . .9-35
Masimo SET Pulse Oximetry (SpO2) Cable Connector . . . . . . . . . .9-36
Temperature/CO Cable Connector . . . . . . . . . . . . . . . . . . . . . . . . . 9-36
Capnostat III (CO2) Cable Connector . . . . . . . . . . . . . . . . . . . . . . . 9-37
NBP Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-38
ECG Cable Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-38
Power Entry Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-39
Network Interface Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-39
Auxiliary Communication Connector . . . . . . . . . . . . . . . . . . . . . . . .9-40
Defib Sync Connector . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-40
Peripheral Expansion Interface Connector . . . . . . . . . . . . . . . . . . . . 9-41
viii Dash 3000/4000 Patient Monitor Revision B
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1 INTRODUCTION

Revision B Dash 3000/4000 Patient Monitor 1-1
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For your notes
INTRODUCTION:
1-2 Dash 3000/4000 Patient Monitor Revision B
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INTRODUCTION: Manual Information

Manual Information

Revision History

Manual Purpose

Intended Audience

Each page of this manual has the document part number and revision letter at the bottom of the page. The revision letter identifies the
document’s update level. The re vision history of this document is summarized below.
Revision History
Revision Date Comment
A 19 December 2002 Initial release of this manual. B 28 February 2002 Corrections were made.
This manual supplies technical information for service representatives and technical personnel so they can maintain the equipment to the assembly level. Use it as a guide for maintenance and electrical repairs considered field repairable. Where necessary the manual identifies additional sources of relevant information and technical assistance.
See the operator’s manual for the in structions necessary to operate the equipment safely in accordance with its function and intended use.
This manual is intended for service representatives and technical personnel who maintain, troubleshoot, or repair this equipment.
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Safety Information

INTRODUCTION: Safety Information

Responsibility of the Manufacturer

General

GE Medical Systems Information Technologies 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.
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 configurati on must meet the requirements of the IEC 60601-1-1 medical electrical systems standard.
Periodically, and whenever the integrity of the device is in doubt, test all functions.
The use of ACCESSORY equipment not complying with the equivalent safety requirements of this equipment may lead to a reduced level of safety of the resulting system. Consideration relating to the choice shall include:
use of the accessory in the PATIENT VICINITY; and
evidence that the safety certification of the ACCESSORY has been performed in accordance to the appropriate IEC 60601-1 and/or IEC 60601-1-1 harmonized national standard.
If the installation of the equipment, in the USA, will use 240V rather than 120V, the source must be a center-tapped, 240V, single-phase circuit.
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INTRODUCTION: Safety Information

Warnings, Cautions, and Notes

The terms danger, warning, and caution are used throughout this manual to point out hazards and to designate a degree or level or seriousness. Familiarize yourself with their definitions and significance.
Hazard is defined as a source of potential injury to a person. DANGER indicates an imminent hazard which, if not avoided, will
result in death or serious injury. WARNING indicates a potential hazard or unsafe practice which, if not
avoided, could result in death or serious injury. CAUTION indicates a potential hazard or unsafe practice which, if not
avoided, could result in minor personal injury or product/property damage.
NOTE provides application tips or other useful information to assure that you get the most from your equipment.
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INTRODUCTION: Safety Information

Equipment Symbols

Some of the following symbols appear on the equipment.
ATTENTION: Consult accompanying documents before using the equipment.
In Europe, this symbol means dangerous or high voltage. In the Unite d States, this symbol represents the caution notice below:
To reduce the risk of electric shock, do NOT remove cover (or back). Refer servicing to qualified personnel.
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 (floa ting ) part. The paddles indica te the equipment is defibrillator proof.
Type B equipment; type B equipment is suitable for intentional external and internal application to the patient, excluding direct cardiac application.
Equipotentiality
Alternating current (AC)
Power;
Fuse
Battery
Indicates the Ethernet connection for the monitor.
I = ON; O= OFF
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INTRODUCTION: Safety Information
PRESS
814A
815A
816A
817A
818A
4P41
Press to open.
POWER
GRAPH GO/STOP
NBP GO/STOP
ZERO ALL
SILENCE ALARM/ADMIT
Medical Equipment With respect to electric shock, fire and mechanical hazards only in accordance with UL 2601-1, and CAN/CSA C22.2 NO. 601.1.
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INTRODUCTION: Service Information

Service Information

Service Requirements

Equipment Identification

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 user’s 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.
Every GE device has a unique serial number for identification. A sample of the information found on a serial number label is shown below.
D 0 XX 0005 G XX
Month Manufactured
A = January B = February C = March D = April E = May F = June G = July H = August J = September K = October L = November M = December
Year Manufactured
0 = 2000 1 = 2001 2 = 2002
(and so on)
Product Code
Two-character product descriptor
Product Sequence Number
Manufacturing number (of total units manufactured)
Division
F = Cardiology G = Monitoring
Device Characterist ics
One or two letters that further describe the unit, for example: P = prototype not conforming to marketing specification R = refurbished equipment S = special product documented under Specials part numbers U = upgraded unit
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2 EQUIPMENT OVERVIEW

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For your notes
EQUIPMENT OVERVI EW:
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Components

Trim Knob
NBP Go/Stop
Zero All
Silence Alarm/ Admit
Graph
Power
Charging Status
A
B
AC Battery
EQUIPMENT OVERVIEW: Components

The Monitoring System

The Patient Monitor

The Dash 3000/4000 patient monitor can function by itself with a built-in writer, or it can be cabled in with the optional Unity Network via Ethernet. Optional components are, if using Wireless LAN or cabled to Ethernet, a Centralscope central station and the Clinical Information Center.
This device is designed to monitor a fixed set of parameters including ECG, noninvasive blood pressure, impedance respiration, SpO2, and temperature. Invasive pressure and EtCO2 are optional features. Additional specialized features include cardiac output, cardiac calculations, pulmonary calculations, dose calculations, PA wedge (PA wedge is only available with the invasive pressure option), ICG module interface, and SAM module interface.
Silence Alarm/
Zero AllNBP Go/StopGraph Go/StopPowerCharging Status
Admit
051C
Dash 3000 Monitor
AB
Dash 4000
001C
Dash 4000 Monitor
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EQUIPMENT OVERVIEW: Components
Right Side View
Left Side View
All of the patient cable connectors are located on the right side of the monitor. A Trim Knob control provides single control operation of virtually all monitor functions.
Patient Cable Connectors
002A
On the left of the monitor, you can find the built-in writer and the battery compartment.
Optional Built-in Writer— The built-in, 4 channel writer is located in the center of the left side of the monitor .
Battery Compartment— The battery packs are located in this compartment.
003A
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EQUIPMENT OVERVIEW: Components
Back View
Network Connector—A cable can be connected to this port for monitors used in patient monitoring network configurations.
Equipotential Terminal—For
measurements in or ne ar the heart we recommend connecting the monitor to the potential equalization system. U se the green and yellow potential equalization cable and connect it to this pin.
AC Power Connector
On the back of the monitor you will find all connectors for equipment and network.
Line V oltage Selector—This s elector is factory set to match the line voltage rating for your country.
Audible Alarm Enunciator—The internal speaker provides sound for audible alarms. For better sound quality do not block speaker.
Aux Port—Used for RAC 2A, other compatible auxiliary devices, and software updates.
Defib Sync Connector—Provides ECG analog output signals to user-supplied equipment. A 5-
004A
volt, 2-millisecond artificial pacer spike is added to the analog output when PACE is on and detection occurs.
Peripheral Expansion Port
Optional Alarm Light Indicator
An optional alarm light indicator can be built into the handle of the Dash 3000 monitor or into the display bezel of the Dash 4000 monitor. When activated, the LED indicator fl ashes red for CRISIS patient status alarms and yellow for WARNING patient status and system alarms.
alarm light indicator
Dash 3000 Monitor
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Dash 4000 Monitor
052B
EQUIPMENT OVERVIEW: Components

User Interface

Flat Panel Display
Tri m Knob Control Power Key
Function Keys
The User Interface consists of a flat panel display and the keypad assembly which consists of a Trim Knob, five function keys, and four LED indicators.
The active-matrix color liquid crystal display (LCD) is assembled into a
shock absorbing isolator that fits within the monitor’s front bezel to protect the display from mechanical shock during use.
The acrylic optical filter protects the display panel from impact and enhances visibility with its non-glare surface coating on the viewing side of the filter. It also has a scratch-resistance surface coating.
The Trim Knob control is a 24-position rotary control with a push selection switch.
The monitor is powered at all times when it is plugged into AC power. When the monitor is not plugged in to AC power, this key turns the
monitor On and Off. When AC power is present, this key toggles the operational mode of the
monitor between normal operation and stand-by mode. In standby mode patient monitoring discontinues. Only the charging function continues and the charging status indicators operate as described below.
Fixed Keys
Four fixed function keys are provided for GRAPH GO/STOP, NBP GO/ STOP, ZERO ALL, and SILENCE ALARM/ADMIT.
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EQUIPMENT OVERVIEW: Components
Indicators
While the monitor powers up or changes between normal mode and standby mode, all four front panel indicators illuminate.
AC Power Indicator
The indicator illuminates green when AC mains power is applied to the monitor (including when the monitor is in the standby mode). The indicator does not illuminate when the monitor is not powered by AC mains power.
Battery Power Indicator
The indicator illuminates yellow when the monitor is operating on battery power. The indicator does not illuminate when the monitor is not battery powered.
Charging Status Indicators
The following table explains what the Charging Status indicators mean.
LED Color Explanation:
Yellow Two battery icons, labeled Charging Status A and B,
illuminate yellow when the respective battery is being charged. If both batteries are present and require charging, then both icons illuminate yellow even though they charge sequentially.
Green The icon illuminates green when the respective
battery is fully charged.
No Light The icon does not illuminate under the following
conditions:
The respective battery is not installed.
The monitor is operating on battery power.
A failure condition has been detected for the respective battery.
“Battery In Use” Indicators
The “Battery In Use” indicator (inside the battery door) illuminates green when the monitor is receiving power solely from the respective battery. The indicators do not illuminate when the monitor is not battery powered.
Neither indicator illuminates when the monitor is operating from both batteries simultaneously (i.e., in a very low battery charge condition when both batteries are joined together in order to sustain operation of the monitor).
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EQUIPMENT OVERVIEW: Components

Optional RAC 2A Module Housing

Optional Dash Port Docking Station

The RAC 2A module housing currently supports the SAM and ICG modules.
797B
An integral power supply is used to run the RAC 2A and support the needed voltages.
The docking station is a quick mount/dismount base for a Dash patient monitor. It gives the monitor easy connect/disconnect access to AC power, the Unity Network, and to auxiliary devices.
NOTE: When a Dash monitor is connected to the docking station, only
the docking station’s Ethernet connector is active. The Dash monitor’s network connector remains inactive until the monitor is disconnected from the docking station.
823A

Optional ICG Module

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The ICG module (impedance cardiography) measures and processes patient hemodynamic data.
825A
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EQUIPMENT OVERVIEW: Components

Optional Wireless LAN System

Access Points
The flexibility of the optional GE Unity Network is increased by using the Wireless LAN system. The Wireless LAN system allows the user to roam from one access point to another, maintaining a strong, seamless connection to the Unity network.
The monitor, with its optional built-in Wireless LAN, functionally performs the same as a monitor connected directly to the optional Unity network. It can be viewed at the central station and by other GE monitors on the network (i.e. Dash 3000/4000, Eagle 4000, and Solar patient monitors). Monitors with Wireless LAN sends and receives patient data via the access points of the Unity network.
NOTE: Wireless patient monitors that are moved from room to room
must have the monitor type configured as Rover or Rover/Combo monitoring.
To integrate the wireless network with the wired network, one or more access points are necessary. An access point connects the wireless monitor to the wired network infrastructure within the building, and acts as a bridge between the wired and wireless networks. The areas covered by each access point overlap to insure continuous coverage.
NOTE: The monitor will only work with a Symbol Access Point. The
monitor will not communicate directly with a Wireless LAN device from Aironet.
050A

Optional Remote Control

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The optional remote control provides all patient monitor controls on a portable component with a Trim Knob control, and allows the user to operate the patient monitor from across the room. Eighteen hard keys are configured for adult, neonatal, or operating room applications.
821A
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EQUIPMENT OVER VIE W : Softwar e Pa ck age s and Sof twar e Op tion s

Software Packages and Software Options

Software Packages
The Dash monitor comes configured with the Basic software package. This package consists of standard-of-care parameters, lethal arrhythmia detection, dose calculations, and features required by clinicians caring for acutely ill patients.
Two additional software packages can be purchased separately or in any combination. These packages provide a variety of features which allow the monitor to be configured to best meet the needs of its intended environment.
The Cardiac software package focuses on cardiac conductivity. Its features include full arrhythmia analysis and storage, as well as ST segment trending, storage, and templates. The ability to adjust the ST measurement point is also included in this package.
The Cardiopulmonary software package centers upon cardiac and pulmonary hemodynamics. Features include the PA insert and wedge algorithms, the intra-aortic balloon pump algorithm, and the thermodilution cardiac output algorithm, including predefined computation constants for the catheters of major manufacturers. Also included are cardiac and pulmonary calculations.
Software Options
Three software options can be purchased separately or in any combination with the software packages and software options.
The High Resolution CRG Trends option provides storage of up to 100 CRG events, and up to 24 hours of CRG trend data, in addition to the CRG feature set found in the Basic software package.
The 12SL ECG analysis program with Gender Specific Criteria and the
Acute Cardiac Ischemia–Time Insensitive Predictive Instrument (ACI­TIPI) analysis option uses recorded ECG data to produce a numerical score which is the predicted probability of acute cardiac ischemia. In addition, the gender specific criteria improves the detection of acute myocardial infarctions (AMI) in women.
The Unity Network option enables you to view other patients on the network, interface with a central station and other network devices, and perform Combo or Rover Combo monitoring.
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EQUIPMENT OVERVIEW: Technical Specifications

Technical Specifications

Due to continual product innovation, specifications are subject to change without notice. The follo win g sp ecifi cat ions are accurate as of t he date of this publication, and pertain to the Dash 3000/4000 Patient Monitor.

Performance Specifications

Display
Size:
Type:
Color: Active-Matrix Liquid Crystal Display (LCD)
Resolution: 640 by 480 pixels
Dash 3000: Dash 4000:
8.4-inch diagonal
10.4-inch diagonal
Controls
Number of traces: 6 (maximum) Number of seconds/trace:
Dash 3000: Dash 4000:
Sweep speed:
All waveforms 6.25, 12.5 or 25 mm/sec (with erase bar)
Waveform display options: Individual 6 waveforms, individual 3 waveforms, full,
Information window: Displays non-real-time information without obstructing
Display organization: Prioritized by parameter
Standard: Trim Knob control plus 5 hard keys: POWER, NBP
Optional remote control Trim Knob control and 18 active hard keys.
4.9 at 25 mm/sec
5.9 at 25 mm/sec
and full grid modes
the display of real-time information
GO/STOP, ZERO ALL, SILENCE ALARM/ADMIT, and GRAPH GO/STOP.
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Alarms
ECG
EQUIPMENT OVERVIEW: Technical Specifications
Categories: Patient Status and System Status Priorities: 4 levels — Crisis, Warning, Advisory, and Message
Notification: Audible and visual Setting: Default and individual Silencing: 1 minute, current alarm only Pause: 5 minutes (adult); 3 minutes (neonatal); 5, 15 minutes,
permanent (OR mode)
Volume: Default 70 dB measured at 1 meter
5 Leadwire cable: I, II, III, V, aVR, aVL, and aVF 10 Leadwire cable (12SL option): V2, V3, V4, V5 and V6 Leads analyzed simultaneously: I, II, III, and V (multi-lead mode) Lead fail: Identifies failed lead Alarms: User-selectable upper and lower heart rate limits Input specifications:
Voltage range: Signal width: Heart rate range: Accuracy: Input impedance:
Common mode: Differential:
Common mode rejection:
Output specifications:
Heart rate averaging: Frequency response:
Display:
Diagnostic Mode:
Monitoring Mode: Moderate Mode: Maximum Mode: Impulse Response:
±0.5 mV to ±5 mV 40 ms to 120 ms (Q to S) 30 to 300 BPM ±1% or ±1 BPM, whichever is greater
>10 MΩ at 50/60 Hz >2.5 M from dc to 60 Hz 90dB minimum at 50 Hz or 60 Hz
8 beats with a 2-second update rate of display Response of non-permanent displays is limited by resolution to 40 Hz (-3dB) @ 25 mm/s. Specified upper frequency limits may vary by ± 2 Hz.
0.67(+0.4 dB) to 100 Hz (-3 dB) For compliance with China National Standard: 1.0 Hz (+0.4 dB) to 75 Hz (-3 dB)
0.67 (+0.4 dB) to 40 Hz (-3 dB)
0.67 (+0.4 dB) to 25 Hz (-3 dB)
5.0 Hz (-3 dB) to 25 Hz (-3 dB) For an impulse of 3 mV applied for 100 ms: Displacement following impulse: < 0.1 mV Slope following impulse: < 0.3 mV/s
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