GEHC Service Manual - MAC 800 RevF v1 2009

GE Healthcare
MAC™ 800
Resting ECG Analysis System
Software Version 1
Operator's Manual
2031504-182 Revision F
© 2008-2009 General Electric Company. All rights reserved.
Archivist, CardioSoft, CASE, Hookup Advisor, MAC, Mactrode, Multi-Link, MUSESilverTRACE, and 12SL
are trademarks owned by GE Medical Systems Information Technologies, a division of General Electric Company going
to market as GE Healthcare. All other marks are not owned by GE and are instead owned by their respective
owners.
NOTE
This manual applies to the MAC™ 800 Resting ECG Analysis System, software version 1. Due to
continuing product innovation, specifications in this manual are subject to change without notice.
This product complies with regulatory requirements of the following European Directive 93/42/EEC
concerning medical devices.
T-2 MAC™ 800 Resting ECG Analysis System 2031504-182F

24 July 2009
Contents
1 Introduction
Manual Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
Purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-2
Intended Audience . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-2
Revision History . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-2
Conventions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
Product References . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
Illustrations and Names . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-3
Safety Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3

Safety Messages. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3
Classification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-10
NRTL Certification Mark . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-10
Biocompatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-10
Legal Notice . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-10
Responsibility of the Manufacturer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-11
General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-11

Recording ECGs During Defibrillation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-11
Accuracy Of the Input Signal Reproduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-12
Modulating Effects in Digital Systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-12
Installation and Connection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-12
Parts and Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-12
Equipment Symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .1-13
Service Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-15
Product Identification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-16
2 Equipment Overview
Equipment Description. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-2
Front View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-2
Side View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3
Back View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-3
Bottom View . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-4
Keyboard Layout . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-5
Acquisition Modules . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-6
Leadwire Adapters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-7
Carrying Handle . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-8
Setting Up the Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8

Inserting the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-9
Connecting the AC Power Adapter . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-9
Connecting Leadwires . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-10
2031504-182F MAC™ 800 Resting ECG Analysis System i

Inserting Paper . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-11
Connecting a Magnetic Card Reader . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-11
Connecting the Barcode Reader . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-11
Connecting the Optional Internal Modem . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-11
Connecting to a LAN . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-11
Connecting an External Laser Printer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-12
Turning on the System . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-12
Configuring the Device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-12
Testing the Device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-12
System Description. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13

Start Up Screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .2-13
Using the MAC 800 Keyboard. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
3 Preparing the Patient

Prepare the Patient’s Skin . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Applying Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3

Standard 12 Lead Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-4
NEHB Lead Placement . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .3-5
4 Entering Patient Information

Entering Patient Information Manually . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
Entering Patient Information with a Barcode Reader . . . . . . . . . . . . . . . . . . . . . . . 4-3
Entering Patient Information with a Magnetic Card Reader . . . . . . . . . . . . . . . . . . 4-4
5 Recording a Resting ECG

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2
Resting ECGs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3

Recording a Resting ECG . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-3
ECG Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-4
Post-Acquisition Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-6
Generating a Rhythm Report (Manual recording) . . . . . . . . . . . . . . . . . . . . . . . . . . 5-8
ECG Reanalysis. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9

Reanalyzing an ECG . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-9
Reanalysis Layout . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-10
Reanalysis Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-11
Hookup Advisor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-12
Special Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-13
ii MAC™ 800 Resting ECG Analysis System 2031504-182F

Recording ECGs of Pacemaker Patients . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-13
Recording ECGs during Defibrillation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .5-14
6 Arrhythmia Mode Recording

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
Arrhythmia Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2

Printing an Arrhythmia Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-2
Arrhythmia Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-3
Printing Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .6-5
Arrhythmia Codes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5
7 RR Analysis
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2
RR Analysis Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2

Printing an RR Analysis Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-2
RR Analysis Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-3
Waveform Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-3
Output Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .7-5
RR Analysis Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-5
8 Managing Internal Storage

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-2
Importing Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3
Printing the File Manager Directory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4
Finding Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4
Editing Patient Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-5
Deleting Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-6
Printing Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-7
Transmitting Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-7
Exporting Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8

Setting Up Export Options . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-9
Exporting Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .8-9
PDF File Naming Convention . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11
2031504-182F MAC™ 800 Resting ECG Analysis System iii

9 System Configuration
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2
Setup Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2

Basic Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-2
Resting ECG Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-5
Arrhythmia Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-12
Communication Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-13
Country Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-17
Patient Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-18
User Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-21
Options Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-23
Service Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-24
Date/Time Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-24
Setup Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-25

Print Setup Report . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-25
Select Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-26
Export Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-27
Import Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-27
Exporting Audit Trail . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .9-28
10 Maintenance
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-2
MAC 800 Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-2

Inspecting the Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-3
Cleaning the Device . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-3
Cable and Leadwire Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-4

Sanitizing Cables and Leadwires . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-4
Storing Cables and Leadwires . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-7
Replacing Leadwire Adapters . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-7
Paper Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-8

Replacing Paper . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-8
Storing Thermal Paper . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-9
Battery Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-9

Battery Safety . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-10
Replacing the Battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-10
Conditioning the MAC 800 Battery Pack . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .10-11
Supplies and accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-12
A Troubleshooting
General Troubleshooting Tips . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-2
iv MAC™ 800 Resting ECG Analysis System 2031504-182F

Equipment Problems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-2
System Will Not Power Up . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-3
ECG Data Contains Noise . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-3
ACI-TIPI Statement is Not Included on Report . . . . . . . . . . . . . . . . . . . . . . . . . . . A-4
Paper Jams . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-4
SD Card Not Present . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-4
Cannot Import or Transmit Records Via Modem . . . . . . . . . . . . . . . . . . . . . . . . . A-5
Cannot Export to Shared Directories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-5
System Errors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-6
B Creating Barcodes
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-2
Setting up the Patient Data Scheme . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-2
Configuring the Barcode Reader. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-3

Configuring the Barcode Reader Manually . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-3
Configuring the Barcode Reader Automatically . . . . . . . . . . . . . . . . . . . . . . . . . . B-4
C Magnetic Card Reader Configuration

Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-2
Understanding the Data Header . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-2
Configuring the Magnetic Card Reader . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-3
Index
2031504-182F MAC™ 800 Resting ECG Analysis System v

vi MAC™ 800 Resting ECG Analysis System 2031504-182F
1 Introduction
2031504-182F MAC™ 800 Resting ECG Analysis System 1-1

Introduction
Manual Information
Purpose
This manual describes the safe and effective operation of the MAC™ 800
Resting ECG Analysis System.
Intended Audience
This manual is written for clinical professionals who use, maintain, and/
or troubleshoot the MAC™ 800 Resting ECG Analysis System. Clinical
professionals are expected to have a working knowledge of appropriate
medical procedures, practices, and terminology used in the treatment of
patients.
Revision History
The document part number and revision appear at the bottom of each
page. The revision identifies the document’s update level.
Revision History, PN 2031504-182
Revision Date Comment
A 11 July 2008 Initial release of document.
B 15 August 2008 Revised document assembly instructions.
C 10 October 2008 Various changes per validation results.
D 5 December 2008 Various changes per pilot site feedback.
E 12 January 2009 Add High-Frequency Device warning.
F 24 July 2009  Updated SD Card information

 Corrected part number for LAN Option
Installation and Troubleshooting Guide
 Updated European address on back
cover
 Updated Equipment Symbols
1-2 MAC™ 800 Resting ECG Analysis System 2031504-182F

Introduction
Conventions
The following conventions are used throughout this manual.
Bold Indicates keys on the keyboard, text to be entered, or hardware items

such as buttons or switches on the equipment.
Italics Indicates software terms that identify menu items, buttons, or

options in various windows.
[Key1] + [Key2] Indicates a keyboard operation. A (+) sign between the names of two
keys indicates that you must press and hold the first key while pressing
the second key once.
For example, “Press Ctrl + Esc” means to press and hold down the
Ctrl key while pressing the Esc key.
Enter Indicates you must press the “Enter” or “Return” key on the keyboard.
Do not type “enter”.
Product References
The name of the product described in this manual is MAC 800 ECG
Analysis System. It will be referred to as “the system” or “the device”
throughout this document.
Illustrations and Names

All illustrations in this manual are provided as examples only. They may
not necessarily reflect your system’s setup or the data on your system.
In this manual, all names appearing in examples and illustrations are

fictitious. The use of any real person’s name is purely coincidental.
Safety Information
Safety Messages
The terms danger, warning, and caution are used throughout this
manual to point out hazards and to designate a degree or level of
seriousness.
Definitions
Familiarize yourself with the safety message definitions and
significance.
Hazard is defined as a source of potential injury to a person.

Introduction
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.
Applicable Messages
The following safety information applies to the MAC 800 ECG Analysis
System.
WARNING
ACCIDENTAL SPILLS — If liquids have entered a
device, take it out of service and have it checked by a
service technician before it is used again.
To avoid electric shock or device malfunction liquids must

not be allowed to enter the device.
WARNING
BATTERY OPERATION — If the integrity of the
protective earth conductor is in doubt, operate the unit
from its battery.
WARNING
STRANGULATION — To avoid possible strangulation,
route all cables away from patient's throat.
WARNING
CONNECTION TO MAINS — This is class I equipment.
The mains plug must be connected to an appropriately

grounded power supply.
WARNING
RF INTERFERENCE — Known RF sources, such as cell
phones, radio or TV stations, and two-way radios, may
cause unexpected or adverse operation of this device
Consult qualified personnel regarding system installation.

Introduction
WARNING
DEFIBRILLATOR PRECAUTIONS — Do not come into
contact with patients during defibrillation. Otherwise,
serious injury or death could result.
Patient signal inputs labeled with the CF symbol with

paddles are protected against damage resulting from
defibrillation voltages.
To ensure proper defibrillator protection, use only

GE-recommended cables and leadwires.
Proper placement of defibrillator paddles in relation to the

electrodes is required to ensure successful defibrillation.
WARNING
ELECTRODES — Polarizing electrodes (stainless steel
or silver constructed) may cause the electrodes to retain a
residual charge after defibrillation. A residual charge will
block acquisition of the ECG signal.
Whenever patient defibrillation is a possibility, use non-

polarizing (silver/silver chloride construction) electrodes
for ECG monitoring.
WARNING
MAGNETIC AND ELECTRICAL INTERFERENCE —
Magnetic and electrical fields are capable of interfering
with the proper performance of the device.
For this reason make sure that all external devices

operated in the vicinity of the device comply with the
relevant EMC requirements. X-ray equipment or MRI
devices are possible sources of interference as they may
emit higher levels of electromagnetic radiation.
WARNING
EXPLOSION HAZARD — Do NOT use in the presence
of flammable anesthetics vapors or liquids.
WARNING
INTERPRETATION HAZARD — Computerized
interpretation is only significant when used in conjunction
with clinical findings.
A qualified physician must overread all computer-

generated tracings.

Introduction
WARNING
OPERATOR — Medical technical equipment such as this
system must only be used by qualified and trained
personnel.
WARNING
SHOCK HAZARD — Improper use of this device
presents a shock hazard. Strictly observe the following
warnings. Failure to do so may endanger the lives of the
patient, the user, and bystanders.
When disconnecting the device from the power line,

remove the plug from the wall outlet first, before
disconnecting the cable from the device; otherwise, there
is a risk of coming in contact with line voltage by
inadvertently introducing metal parts in the sockets of the
power cord.
Devices may be connected to other devices or to parts of

systems only after making certain that there is no danger
to the patient, the operators, or the environment as a
result. Standards IEC 60601-1-1/EN60601-1-1 must be
complied with in all cases.
WARNING
DROPPING HAZARD — For devices installed above the
patient, adequate precautions must be taken to prevent
them from dropping on the patient.
WARNING
PACKAGING DISPOSAL — Dispose of all packaging
material, observing all applicable waste control
regulations and keeping out of children’s reach.
WARNING
ELECTRIC SHOCK — To reduce the risk of electric
shock, do NOT remove cover (or back).
Refer servicing to qualified personnel.

Introduction
WARNING
BURN PROTECTION — To ensure defibrillator
protection and protection against high-frequency burns,
use only GE-recommended cables and leadwires.
Otherwise, serious injury could result.
WARNING
HIGH-FREQUENCY PRECAUTIONS — Do not use the
device with high-frequency surgical units.
CAUTION
ACCESSORIES (SUPPLIES) — To ensure patient
safety, use only parts and accessories manufactured or
recommended by GE.
Parts and accessories used must meet the requirements of

the applicable IEC 60601 series safety standards and
essential performance standards, and/or the system
configuration must meet the requirements of the IEC
60601-1-1 medical electrical systems standard.
CAUTION
PROPER LEADWIRE CONNECTION — Improper
connection will cause inaccuracies in the ECG.
Trace each individual leadwire from its acquisition

module label to the colored connector and then to the
proper electrode to ensure that it is matched to the correct
label location.
CAUTION
TRIPPING HAZARD — To avoid tripping injuries, keep
patient cables off the floor and route them away from
patient legs and the healthcare provider’s work area.

Introduction
CAUTION
ACCESSORIES (EQUIPMENT) — 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.
CAUTION
BEFORE INSTALLATION — Compatibility is critical to
safe and effective use of this device. Please contact your
local sales or service representative prior to installation to
verify equipment compatibility.
CAUTION
DISPOSABLES — Disposable devices are intended for
single use only. They should not be reused as performance
may degrade or contamination could occur.
CAUTION
PRODUCT DISPOSAL — At the end of its service life,
the product described in this manual, as well as its
accessories, must be disposed of in compliance with local,
state, or federal guidelines regulating the disposal of such
products.
If you have questions concerning disposal of the product,

please contact GE or its representatives.
CAUTION
EQUIPMENT DAMAGE — Devices intended for
emergency application must not be exposed to low
temperatures during storage and transport to avoid
moisture condensation at the application site.
Wait until all moisture has vaporized before using the

device.

Introduction
CAUTION
OPERATOR — Medical technical equipment such as
this electrocardiograph system must only be used by
persons who have received adequate training in the use of
such equipment and who are capable of applying it
properly.
CAUTION
POWER REQUIREMENTS — Before connecting the
device to the power line, check that the voltage and
frequency ratings of the power line are the same as those
indicated on the unit's label. If this is not the case, do not
connect the system to the power line until you adjust the
unit to match the power source.
In the U.S.A., if the installation of this equipment will use

240V rather than 120V, the source must be a center-
tapped, 240V, single-phase circuit.
This equipment is suitable for connection to public mains

as defined in CISPR 11.
CAUTION
RESTRICTED SALE — U.S. federal law restricts this
device to sale by or on the order of a physician.
CAUTION
SERVICEABLE PARTS — This equipment contains no
user serviceable parts. Refer servicing to qualified service
personnel.
CAUTION
SUPERVISED USE — This equipment is intended for
use under the direct supervision of a licensed health care
practitioner.
CAUTION
EQUIPMENT CONFIGURATION — The equipment or
system should not be used adjacent to, or stacked with
other equipment.
If adjacent or stacked use is necessary, test the equipment

or system to verify normal operation.

Introduction
Classification
The unit is classified, according to IEC 60601-1, as follows:
Type of protection against Class I, internally powered equipment

electrical shock
Degree of protection Type CF defibrillation-proof applied part

against electrical shock
Degree of protection Ordinary Equipment (enclosed equipment without

against harmful ingress of protection against ingress of water).
water
Degree of safety of Equipment not suitable for use in the presence of a

application in the presence flammable anesthetic mixture with air or with oxygen or
of a flammable anesthetic nitrous oxide
mixture with air or with
oxygen or nitrous oxide
Method(s) of sterilization or Not applicable

disinfection recommended
by the manufacturer
Mode of operation Continuous operation
NRTL Certification Mark
Medical Equipment
With respect to electric shock, fire and mechanical

hazards only in accordance with UL 60601-1, and
CAN/CSA C22.2 NO. 601.1.
Biocompatibility
The parts of the product described in this operator’s manual, including
all accessories, that come in contact with the patient during the intended
use, fulfill the biocompatibility requirements of the applicable standards.
If you have questions in this matter, please contact GE or its
representatives.
Legal Notice
Our equipment contains several fields which can be filled in before
performing an ECG. While some of these fields are required, some are
optional and left to the user to assess whether they are needed to
perform the exam. A field RACE is one of these optional fields. It has
been acknowledged by the medical profession as useful to analyze some

Introduction
pathologies. You should be aware that, in some jurisdictions, the

processing of data revealing an individual’s racial origin is subject to
legal requirements, such as obtaining the patient’s prior consent. If you
elect to collect this type of data, it is your responsibility to ensure that
you comply with all applicable legal requirements.
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 Information
Recording ECGs During Defibrillation
It is not necessary to remove the ECG electrodes prior to defibrillation;
the patient signal is defibrilation-proof.
Use silver-silver chloride electrodes. A defibrillator discharge may cause

stainless steel or silver electrodes to retain a residual charge, which
could cause a polarization that will block the acquisition of the ECG
signal for several minutes.
We recommend using non-polarizing disposable electrodes with

defibrillation recovery ratings as specified in AAMI EC 12.3.2.2.4
(SilverTRACE family of electrodes). AAMI EC12 requires that the
polarization potential of an electrode pair does not exceed 100 mV
5 seconds after a defibrillation discharge.
If other electrodes are used, disconnect the patient cable from the system
before delivering the defibrillation shock.
NOTE
If excessive DC voltages are present at the electrode, then a message
will appear indicating a Lead Off condition.
ADS (cubic spline correction) can cause a signal delay of approximately 2

seconds; therefore they should be disabled if the patient has to be
defibrillated while the ECG is being recorded.

Introduction
Accuracy Of the Input Signal Reproduction

 Overall System Error is tested using the method described in
AAMI EC11 3.2.7.1. Overall System Error is less than +/-5%.
 Frequency Response is tested using the method described in
AAMI EC11 3.2.7.2 methods A and D.
Modulating Effects in Digital Systems

This device uses digital sampling techniques that may produce some
variation in amplitudes of Q, R, and/or S waves from one heart beat to
the next, which may be particularly noticeable in pediatric recordings. If
this phenomenon is observed, the clinician should be aware that the
origin of amplitude variations is not entirely physiologic. For measuring
voltages of Q, R, and S waves, it is advisable to use the QRS complexes
with the largest deflection of the particular waves.
Installation and Connection

If the installation of this equipment, in the USA, will use 240 V rather
than 120 V, the source must be a center-tapped, 240 V, single-phase
circuit.
Contact GE for information before connecting any devices to this

equipment not recommended in this manual.
Parts and Accessories

To ensure patient safety, use only parts and accessories manufactured or
recommended by GE. Browse to www.gehealthcare.com to obtain
information about GE-recommended supplies and accessories.
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.
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.

Introduction
Equipment Symbols
The following symbols may appear on the product, its packaging, and or
its documentation.
Defibrillation-proof type CF equipment.
Equipotential ground point
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.
Attention, see instructions for use
Consult instructions for use.
Catalogue (part) number.
Serial number.
Date of manufacture.
Manufacturer address.
Recyclable.
Atmospheric limits.
Temperature limits.
Humidity limits.

Introduction
Keep dry.
Fragile.
Alternating current.
Battery symbol. The flashing amber LED next to this symbol indicates you
must connect the system to AC power to re-charge the battery.
Push button to turn device on, off, or standby
Leads key. Used to change the leads when the screen is being used to
display waveforms.
ECG key. Used to acquire a resting ECG, to print a 10-second report in
Arrhythmia mode.
Rhythm key. Used to print a continuous, real-time rhythm ECG rhythm
strip. Press the Stop key to stop the rhythm strip from printing. (Rhythm
report is not stored and can not be transmitted.)
Stop key. Used to stop the writer from printing.
Cursor control keys. Push to change or select the displayed menu item.
Enter button. Push to change or select the displayed menu item.
Environment-friendly Use Period per Chinese standard SJ/T11363-2006

(China specific).
Secure Digital (SD) Card.
Batch or lot number.
Authorized European Representative.
CCC Mark - China Compulsory Certification mark
TÜV Rheinland NRTL Certification Mark.
China Metrology Certification.
Indicates conformity with applicable European directives.

Introduction
IP20 The International Protection (IP) rating indicates the device’s

classification against solid and liquid ingress per IEC/EN 60529. The
classification format is IPxy and is defined as follows:
 x indicates the classification for solid objects according to the

following list:
 0 – Not protected
 1 – Protected against objects >= 50mm in diameter
 2 – Protected against objects >= 12.5mm in diameter
 3 – Protected against objects >= 3.5mm in diameter
 4 – Protected against objects >= 1.0mm in diamter
 5 – Dust protected
 6 – Dust tight
 y indicates the classification for liquid according to the following list:
 0 – Not protected
 1 – Protected against vertical dripping
 2 – Protected against dripping with a 15 degree tilt
 3 – Protected against spraying
 4 – Protected against splashing
 5 – Protected against jetting
 6 – Protected against powerful jetting
 7 – Protected against immersion up to 1 minute
 8 – Protected against immersion beyond 1 minute
PCT. GOST marking symoblizing conformity with applicable Russian
Gosstandart technical and safety standards.
USA only.
For use by or on the order of a Physician, or persons licensed by state

law.
Service Requirements
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.

Introduction
Product Identification
Every GE Healthcare product carries a serial number label that
identifies the model, the product code, and the unit’s serial number, as
seen in the following illustration and table.
A Date of manufacture in YYYY-MM format.
B Product part number.
C Product description code.
D Unit serial number.
The following illustration and table identify the basic structure of the
serial number itself.
A The product code for MAC 800 systems is SDS.
B Year Manufactured (00-99): 07 = 2007, 08 = 2008, and so on.
C Fiscal Week Manufactured
D Production Sequence Number
E Manufacturing Site
F Miscellaneous Characteristic

2 Equipment Overview

Equipment Overview
Equipment Description
Front View
005
Name Description
A Display Presents waveform and text data.
B Power LED Indicates the unit is plugged in and receiving power.
C Battery LED Indicates various battery states:
 Solid amber light indicates the battery is charging.

 Flashing amber light indicates the battery is low.
 Off indicates the battery is neither charging nor low.
D Operating LED Indicates the system is running.
E Keyboard Input device for controlling the system or entering data.
See “Keyboard Layout” on page 2-5 for more information.
F Writer Prints reports.

Equipment Overview
Side View
004
Name Description
A ECG signal input connector D-sub 15-pin female connector for the
acquisition cable.
B SD card slot Secure Digital card slot. Insert card as indicated

by the icon. The MAC 800 system supports only
SD cards formatted for FAT or FAT16 file
systems.
Back View
003
Name Description
A Modem Port RJ11 connector from the optional internal modem to an

analog telephone line.
B LAN connection RJ45 network LAN connector. The LEDs indicate LAN
status.
 The green LED right of this port indicates a good

Ethernet connection.
 The amber LED left of this port flashes indicates
network traffic.

Equipment Overview
Name Description
C USB connector Universal Serial Bus connector for USB devices, such
as the optional barcode reader, a magnetic card
reader, or an external USB keyboard.
D COMM Port Serial connector for data communication with CASE/

CardioSoft or MUSE system with a serial cable.
E AC power connection Standard connector for the AC power cable.
F Equipotential grounding Connect non-grounded peripheral devices to ensure

lug equipotential.
Bottom View
066A
Name Description
A Battery Rechargeable lithium-ion battery.
B Carrying handle Handle for carrying the MAC 800 unit.

Equipment Overview
Keyboard Layout
Your keyboard may differ slightly from that shown.
002
Name Description
A Function Keys Selects menu options on the screen. Refer to

(F1 through F6) “Selecting Menu Options” on page 2-13 for details.
B Leads key Changes the leads when the screen is being used to
display waveforms.
C Power Button Turns the unit on and off.
D ECG key Acquires a resting ECG and prints a 10-second report

in Arrhythmia mode.
E Trimpad The arrows move the cursor left, right, up, or down.
The center button moves the focus within a window or
selects the currently active item.
F Rhythm key Prints a continuous, real-time rhythm ECG strip. Press

the Stop key to stop the rhythm strip from printing.
(Rhythm report is not stored and cannot be
transmitted.)
G Stop key Stops the writer from printing.
H Backspace Key Deletes characters.
I Space Key Adds a space between typed characters.
J T9 key Switches between different input methods. For more

information, refer to “Entering Data Using the T9 key”
on page 2-14.

Equipment Overview
Acquisition Modules
The MAC 800 system supports a variety of acquisition modules.
041A
WARNING
BURN PROTECTION — To ensure defibrillator
protection and protection against high-frequency burns,
use only the acquisition cable that ships with this
equipment.
Otherwise, serious injury could result.
CAUTION
Trace each individual leadwire from its acquisition cable

label to the colored connector and then to the proper
electrode to ensure that it is matched to the correct label
location.

Equipment Overview
Name Description
A D-Sub 15-pin male Connects to the system’s ECG signal input connector.
connector One end of each acquisition cable consists of a D-sub
15-pin male connector.
B Multi-link Acquisition The lead end of the multi-link acquisition cable

Cable Leads attaches to the leadwire adapters and uses 10 or 12
leadwires.
C NEHB Acquisition The lead end of the NEHB acquisition cable attaches to
Cable Leads the leadwire adapters and uses 12 leadwires.
D Value Acquisition Cable The lead end of the value acquisition cable consists of
Leads 10 leadwires.
Leadwire Adapters
The leadwires require an adapter to connect to an electrode, as shown in
the following illustration.
010
A leadwire end
B 4 mm pin
C grabber
D mactrode clip

Equipment Overview
Carrying Handle
When you need to move the system, you can use the handle for
convenience. Use the following steps to use the handle correctly
067A
Setting Up the Equipment

Setting up the MAC 800 system consists of the following steps:
1. Inserting the battery.

2. Connecting the AC power adapter.
3. Connecting leadwires.
4. Inserting paper.
5. Connecting a magnetic card reader.
6. Connecting a barcode reader.
7. Connecting the optional internal modem.
8. Connecting the LAN.
9. Connecting the external laser printer.
10. Turning on the unit.
11. Configuring the system.
12. Testing the equipment.
Each step is described in more detail on the following pages.

Equipment Overview
Inserting the Battery

The MAC 800 system is shipped with a lithium-ion battery that is
charged when inserted into a MAC 800 system connected to AC power.
1. Gently turn unit over and find the empty battery compartment.
2. Insert the battery as shown.
NOTE
The battery charges when it is inserted in a MAC 800 system that is
connected to AC power. You may begin using the system connected to
AC power. However, do not use the system on battery power until the
battery is fully charged as indicated by the on-screen battery gauge
and the solid amber LED next to the display.
Connecting the AC Power Adapter

The MAC 800 system can run using AC or battery power. When the unit
is plugged into an AC outlet, it uses AC power and charges the installed
battery.
NOTE
The system should be connected to an independent power socket and
used alone in the patient environment.
Use the following instructions to connect the system to an AC power

outlet.
042A
1. Connect the female end of the unit’s power cord to the AC power
connector on the back of the unit. (A)

Equipment Overview
2. Plug the male end of the unit’s power cord into an AC outlet. (B)
3. Check the Power LED to make sure the unit is receiving power from
the AC outlet.
For more information, refer to “Front View” on page 2-2.
Connecting Leadwires
Use the following instructions to connect your leadwires and acquisition
module to the MAC 800 unit.
WARNING
ELECTRICAL SHOCK — To avoid potential injury
resulting from electrical shock, DO NOT attempt to
connect the patient cables directly to an AC power outlet.
Connect patient cables only to the ECG Signal Input

Connector on the MAC 800 unit, as described in the
following procedure.
011A
1. Assemble the leadwires and adapters.
Refer to “Replacing Leadwire Adapters” on page 10-7 for details.
2. Connect the leadwires to the front of the acquisition module. (A)
Refer to “Acquisition Modules” on page 2-6 for more information.
3. Connect the acquisition cable to the MAC 800 system. (B)
Ensure the cable is seated snugly.

Equipment Overview
Inserting Paper
Before printing ECG reports, insert the MAC 800 110mm z-fold paper.
Refer to “Replacing Paper” on page 10-8 for instructions.
Connecting a Magnetic Card Reader

The MAC 800 system supports third-party magnetic card readers
capable of reading magnetic strips that adhere to ISO 7810, 7811-1,
7811-2, 7811-3, 7811-4, and 7811-5 standards. To use a third-party card
reader with the system, connect it to the MAC 800 system’s USB port.
Refer to the magnetic card reader’s documentation for additional
information.
NOTE
Do not connect a magnetic card reader if the bar code reader option
(BCRD) is enabled. If the BCRD option is enabled, the system will
expect a bar code reader and the magnetic card reader will not
function correctly.
Connecting the Barcode Reader

If the optional barcode reader was purchased with the unit, connect it to
the MAC 800 system’s USB port. Refer to the barcode reader’s
documentation for additional information.
NOTE
The BCRD option, which must be enabled in the system in order to
use the reader, is activated at the factory when the barcode reader is
purchased with the unit. However, the barcode settings must be
configured for the site before the reader can be used. Refer to
“Patient Setup” on page 9-18 for details.
Connecting the Optional Internal Modem

If the MAC 800 system was purchased with the internal modem option,
connect the modem to an analog phone line using the RJ11 connector on
the back of the unit. See “Back View” on page 2-3 for details.
Connecting to a LAN
If the LANC (LAN Communication to Cardiosoft) or LANM (LAN
Communication to MUSE) options were purchased, connect an ethernet
cable to the RJ45 network connector on the back of the MAC 800 unit.
See LAN Option Installation and Troubleshooting Guide
(PN 2020299-025) for information on configuring the LAN connection.
NOTE
If the MAC 800 unit will be used as a mobile unit, do not connect the
device to a LAN until you are ready to import, transmit, or export
records.

Equipment Overview
Connecting an External Laser Printer

The MAC 800 system can be used with an external laser printer
connected to its USB port. The printer must be used away from the
patient vicinity and must:
 be compliant with IEC60950 or equivalent standards,

 be compliant with the PCL5e language or higher,
 have a minimum of 600 dpi resolution, and
 have a minimum of 8 MB memory.
Refer to the printer’s documentation for setup information.
Turning on the System

Press the Power button to power on the system. Verify the following:
 The Power LED lights.

 The selected MAC 800 startup screen appears with no errors.
If you encounter any problems powering on the system, refer to

Appendix A for troubleshooting instructions.
Configuring the Device

When the device is ready for operation, configure the system settings
using the information in Chapter 9.
If the same settings will be applied to multiple devices at the site, export
the settings to an SD card and use that card to import the settings to
other MAC 800 systems.
Testing the Device

After the MAC 800 unit has been set up and configured, test the device
completely before using it with patients. Test scenarios include:
 Conducting and printing a resting ECG

Refer to Chapter 5 for instructions on resting ECGs.
 Conducting and printing an arrhythmia ECG
Refer to Chapter 6 for instructions on arrhythmia ECGs.
 Conducting and printing an RR analysis
Refer to Chapter 7 for instructions on RR Analysis.
 Saving, importing, printing, deleting, transmitting, and exporting
records
Refer to Chapter 8 for instructions on using internal storage.

Equipment Overview
System Description
Start Up Screen
Depending on what options have been selected for Power up mode in
Basic Setup, the start up screen will be one of the following:
 Resting ECG
 Arrhythmia
 Main Screen
 A window prompting you to enter User ID and Password.
NOTE
The password window will appear only if the High Security Mode
option is selected in Basic Setup. The system can be used to take
a STAT ECG without having to log in. Press the STAT ECG
softkey to begin taking an ECG without logging into the MAC
800 system.
Using the MAC 800 Keyboard

You interact with the MAC 800 system by using the keyboard to:
 Enter data
 Select menu options
 Navigate through data entry fields
For a complete description of the MAC 800 keyboard features, refer to
“Keyboard Layout” on page 2-5. For information on entering data using
the keyboard, refer to “Entering Data Using the T9 key” on page 2-14.
Selecting Menu Options

Configure the device and initiate ECG readings by selecting menu
options that appear across the bottom of the display. Up to six menu
options may be available at any given time, and each option corresponds
to a function key (F1–F6) directly below the display.
043A

Equipment Overview
Press a function key to select the corresponding menu option. Depending

on the selected option, one of the following results occurs:
 Start an ECG
For example, selecting the Resting ECG menu option opens the
Resting ECG function.
 Change a setting
For example, during a resting ECG, selecting the 25 mm/s option
changes the speed of the reading.
 Open a window
For example, the Patient Data option opens the Enter Patient Data
window.
 Save your selections
After entering data or changing a configuration, you may have the
option to save your changes by selecting the Save menu option.
Navigating Data Entry Windows

Use the trimpad to navigate through data entry windows.
Press the arrows to move the cursor left, right, up, and down through the
fields.
Press the center button to select the current field. If the field is
associated with a list of valid values, that list will be displayed.
Entering Data Using the T9 key

Twenty-six letters are mapped to 8 numeric keys (from 2 to 9). Pressing a
key multiple times cycles through each letter associated with that key.
For example, ACE is entered by pressing 2 222 33. Because mapping is
many-to-one, converting number sequences to a word can be ambiguous.
T9 Text Input is available in the following languages: Chinese

(Simplified), Czech, Danish, Dutch, English, Finnish, French, German,
Hungarian, Italian, Japanese, Korean (Hangul), Norwegian, Polish,
Portuguese, Russian, Slovak, Spanish, and Swedish.
Use the following instructions to input information using the T9 key
1. To input numbers, press the T9 key until the input method indicator
is “123” and then press 0 through 9 to enter numbers.

Equipment Overview
2. To input letters, press the T9 key until the input method indicator is
“ABC” (for uppercase) or “abc” (for lowercase) and then press 2
through 9 to enter the corresponding letters printed on the keys.
Press 0 to enter a space.
To toggle through the available letters, press the key repeatedly in

succession. When the desired letter is displayed, pause before
pressing the next key.
3. To input symbols, press the T9 key until the input method indicator
is “@” and press 1 to display the available symbols.
Available symbols are:
To toggle through the available symbols, use the left and right
arrows on the trimpad until the desired symbol is displayed. Press
the central button on the trimpad to select the symbol.
4. To delete a character, press the backspace key.

Equipment Overview

3 Preparing the Patient

Preparing the Patient
Prepare the Patient’s Skin

Careful skin preparation is the key to an interference-free ECG. The
signal quality is shown on the Hookup Advisor indicator.
25A
1. Shave any hair from each electrode site and degrease each electrode
site with alcohol.
2. Apply electrode to prepared area.
WARNING
SHOCK HAZARD — Ensure that conductive parts of the
electrodes or lead wires do not come in contact with other
conductive parts, including earth.
This would cancel the protection provided by the isolated

signal input.
WARNING
SHOCK HAZARD — The operator shall not touch the
SIP (Signal Input Part) / SOP (Signal Output Part) and
the patient simultaneously.

3. Verify the leads are all connected and working properly.
NOTE
You can use the Hookup Advisor to review connection quality
before beginning the ECG. For more information, refer to
“Hookup Advisor” on page 5-12.
Applying Electrodes
The placement of electrodes varies depending on whether you wish to
acquire a standard 12-lead ECG or an NEHB ECG. Both methods are
described in this section.
WARNING
ELECTRICAL SHOCK — To avoid electrical shock, do
not touch the SIP/SOP (Signal Input Part/Signal Output
Part) and the patient simultaneously.
CAUTION
Trace each individual leadwire from its acquisition

module label to the colored connector and then to the
proper electrode to ensure that it is matched to the correct
label location.

Standard 12 Lead Placement

To acquire a standard 12 lead ECG, use the placement shown in the
following illustration.
026A
AHA
IEC Label Electrode Placement
Label
A V1 red C1 red Fourth intercostal space at the right sternal border.
B V2 yellow C2 yellow Fourth intercostal space at the left sternal border.
C V3 green C3 green Midway between location B and D.
D V4 blue C4 brown Mid-clavicular line in the fifth intercostal space.
E V5 orange C5 black Anterior axillary line on the same horizontal level as

D.
F V6 purple C6 purple Mid-axillary line on the same horizontal level as D

and E.
G LA black L yellow Left deltoid. (Alternate placement: left wrist.)
H LL red F green Above left ankle. (Alternate placement, upper leg as

close to torso as possible.)
I RL green N black Above right ankle. (Alternate placement, upper leg as

close to torso as possible.)
J RA white R red Right deltoid. (Alternate placement: right wrist.)

NEHB Lead Placement

To acquire a NEHB ECG, use the standard 12 lead electrode placement
and items A and B as shown in the following figure.
027A
AHA
IEC Label Electrode Placement
Label
A A1 orange Nst white Attachment point of the 2nd rib to the right sternal
edge.
B A2 orange Nax white 5th intercostal space on the left posterior axillary line.
(Same position as V7 or C7.)
C V4 blue Nap white Mid-clavicular line in the fifth intercostal space.

(Same position as C4.)


4 Entering Patient
Information

Entering Patient Information
Entering Patient Information Manually

Patient information should be entered for each new patient from whom
readings are taken. Use the following procedure to enter the information
if you do not use a barcode reader or magnetic card reader, or if you want
to modify or add to the patient data entered with a barcode reader or
magnetic card reader.
CAUTION
ACCURATE PATIENT INFORMATION — Patient
information may be retained from a previous patient. Be
sure to check the patient information screen for each new
patient. Data assigned to the wrong patient causes
erroneous patient information that can affect diagnosis
and treatment of the patient(s).
Make sure that you enter patient information for the

correct patient.
1. Open the Enter Patient Data window.
For Resting ECG and RR Analysis, the window is opened by pressing

the Patient Data softkey.
For Arrhythmia ECGs, the window opens automatically when you

initially select the application. For subsequent patients, press Stop
Recording > Confirm Stop > More > Start Recording > New Patient to
reopen the Enter Patient Data window.
2. Enter the necessary patient information. or press the Patient List

softkey to select a patient from a list of patients.
Refer to “Entering Data Using the T9 key” on page 2-14 for

additional information on entering data.
NOTE
The Patient List is available only if the optional internal storage
is enabled.
If you select a patient from the patient list, only the first page of
patient information is reused: all subsequent pages must be
entered manually.
3. Use the Page Up and Page Down softkeys to move backward and
forward through the patient data windows, respectively.
NOTE
If the CTDG (Clinical Trial Data Guard) option is activated, you
enter clinical trial data on the last window.
4. When all the patient data has been entered, press the Save softkey to
save the data.

Entering Patient Information with a Barcode Reader

Using a barcode reader can simplify the entry of patient information and
reduce the introduction of errors. When you scan a patient’s barcode, it
retrieves the patient information encoded in the barcode. You can then
verify or modify the information as appropriate.
To use the barcode reader, it must be connected to the USB port on the
MAC 800 back panel and properly configured. Refer to Chapter 9 for
instructions on setting up the optional barcode reader.
1. When the Scan the Patient Barcode prompt appears on the screen,
scan the patient’s barcode.
044A
A Please wait message is displayed on the screen and the barcode
reader beeps. The first Patient Data window opens with the data
from the patient’s barcode entered in the appropriate fields.
2. Confirm that the data entered from the patient’s barcode is accurate.
3. Enter or modify patient information as necessary.
Refer to “Entering Patient Information Manually” on page 4-2 for

details.
4. After verifying that the patient information is correct, press the Save
softkey to save the patient data.

Entering Patient Information with a

Magnetic Card Reader
Using a magnetic card reader can simplify the entry of patient
information and reduce the introduction of errors. When you swipe a
patient’s magnetic card, it retrieves the patient information encoded in
the card’s magnetic strip. You can then verify or modify the information
as appropriate.
To use a magnetic card reader, it must be connected to the USB port on

the MAC 800 back panel and properly configured. Refer to Chapter 9 for
instructions on setting up a third-party magnetic card reader.
1. When the Swipe the Patient Card prompt appears on the screen,
swipe the patient’s magnetic card through the card reader.
044A
A Please wait message is displayed on the screen. After the data has
been processed, the first Patient Data window opens with the data
from the patient’s card entered in the appropriate fields.
2. Confirm that the data entered from the patient’s card is accurate.
3. Enter or modify patient information as necessary.
Refer to “Entering Patient Information Manually” on page 4-2 for

details.
4. After verifying that the patient information is correct, press the Save
key to save the patient data.

5 Recording a
Resting ECG

Recording a Resting ECG
Introduction
The Resting ECG function is part of the basic MAC 800 system. Resting
ECG mode is the default Power up mode. When the system is turned on,
the Resting ECG display will appear, similar to the following figure. The
default can be modified in the Basic Setup.
045A
Resting ECG Display
Item Name Description
A ECG Type Type of ECG. Valid types are Resting ECG,

Arrhythmia, and RR Analysis.
B Display Format Format of current waveforms. Press the Leads key

to cycle through all 12 leads.
C Date Current system date.
D Time Current system time.
E Battery status indicator Displays the current battery level. Appears only
when the unit is operating on battery.
F Internal storage indicator Appears only if the internal storage option is

enabled. Format is:
Approximate number of ECG records that can be

stored in remaining memory / Maximum number of
ECG records that can be stored

Resting ECG Display (Continued)
Item Name Description
G Hookup Advisor Indicator See “Hookup Advisor” on page 5-12 for more
information.
H Patient’s Heart Rate Current patient heart rate measured in beats per
minute.
I Menu Options The available menu options. The list of available

options changes depending on the function and the
current location within that function. For more
information, refer to “Selecting Menu Options” on
page 2-13.
J Lead Labels Identifies each waveform and indicates waveform

quality. Yellow = noisy lead.
Red = disconnected lead.
Resting ECGs
A resting ECG is the default mode of the MAC 800, although this may be
changed in the system configuration. This section describes how to record
a resting ECG as well as the available options.

The following steps describe how to conduct a resting ECG.
NOTE
To take a stat ECG, do one of the following.
 If the password screen is displayed, press the STAT ECG softkey.

 If the password screen is not displayed, skip directly to step 7.
1. Prepare the patient as described in Chapter 3.
2. Verify the system is in Resting ECG mode.
If the system is not in the Resting ECG mode, press the Resting ECG
softkey at the Main Menu.
3. Enter the patient data as described in Chapter 4.
4. Adjust the Speed, Gain, and Low Pass Filter until the waveforms are
configured as desired.
For more information, refer to “ECG Options” on page 5-4.
5. If the patient has a pacemaker, press the Pace Enhance softkey.

6. Press the Leads key to scroll through the leads or change the lead
format.
For more information on display formats, refer to “Resting ECG

Setup” on page 9-5.
7. When the waveforms are configured, press the ECG key to begin the
acquisition.
A progress bar indicates the percentage of the data acquired. When

the acquisition is complete, one of two things will occur, depending
on the setting of the Preview Before Analysis option on the Resting
ECG Setup window.
 If the Preview Before Analysis option is enabled, a preview of the

10 second ECG is shown on the display. Proceed to step 8.
 If the Preview Before Analysis option is not enabled, the ECG
data will be analyzed and printed after it has been acquired. Skip
to step 9.
8. While reviewing the preview, do one of the following.
 To discard the reading and begin over, press Cancel and repeat
from step 4.
 To accept the reading, press Continue.
The menu options change to allow you to manage the acquisition.
Proceed to step 9.
 To print the reading to a laser printer attached to the device,
press Laser Print.
The ECG is saved and printed on the laser printer. You return to
the main ECG screen, where you can take another ECG.
9. Use the options to edit patient information, to print a copy, or to
save, transmit, or reanalyze the data.
For more information on each option, refer to “Post-Acquisition

Options” on page 5-6.
ECG Options
The MAC 800 provides several options for configuring an ECG. The
options, presented as option keys across the bottom of the display, are
listed in the following table.

Option Description
Patient Data Opens the patient data entry window.
Sweep Speed Changes the speed of the waveform on the display and printout.
Changing the speed also changes the speed the wiper bar moves
across the display.
Measurement is in millimeter per second (mm/s) and includes the

following options:
 25 mm/s
 50 mm/s
 12.5 mm/s - 5 mm/s
When the option includes two speeds (12.5 mm/s - 5 mm/s), the
first speed is for the display and the second speed is for the
printout.
Gain Changes the amplitude of the ECG signal on the display or in the
report. Measurement is in millimeter per millivolt (mm/mV) and
includes the following options:
 5 mm/mV
 10 mm/mV
 20 mm/mV
 40 mm/mV
 2.5 mm/mV
 Automatic
The larger the selected measurement, the larger the waveform
appears. Only the appearance of the waveform changes; signal
strength is not affected.
NOTE
If Automatic is selected, the system calculates the best gain
based on the peak-to-peak amplitudes of all displayed leads
and the selected display format.

Option Description
Filter Eliminates noise in the waveform by restricting which frequencies

are included. Frequencies are measured in Hertz (Hz) and
include the following options:
 20 Hz
 40 Hz
 100 Hz
 150 Hz
Selecting a frequency eliminates signals that exceed that
frequency. The smaller the frequency selected, the more signal is
filtered out. For example, a filter of 40 Hz displays only signals at
40 Hz or less; signals greater than 40 Hz will be ignored.
CAUTION
INACCURATE READINGS — Using the filter can result in a
cleaner waveform, but selecting a frequency that is too low could
alter the waveform’s morphology, resulting in an inaccurate
reading.
To avoid this, use the filter only to eliminate excessive noise and
use the highest frequency that provides a readable waveform.
Pace Enhance Standardizes the pace spike. Options are On and Off.
More Toggles between the first row of options (above) and the second
row of options (below).
Printer Leads Selects which leads to include in the printout. Options are:
 First Six
 Second Six
 Rhythm Six
Used only when conducting rhythm ECGs. Refer to “Generating a
Rhythm Report (Manual recording)” on page 5-8 for more
information.
Main Menu Exits the Resting ECG function and returns to the Main Menu.
Post-Acquisition Options
In addition to setup options, the Resting ECG functionality offers
additional options after the ECG has been acquired. Presented as option
keys across the bottom of the display, they are listed in the following
table.

Option Description
Page 1
Next Patient Opens the patient entry window to allow you to enter or select a
new patient.
Print Prints the ECG report.
Save Stores the current ECG report. Not available in either of the
following conditions:
 neither the M100 nor M300 internal storage option is

enabled, or
 ECGs are set up to save automatically.
Transmit Sends the current ECG report to the location defined on the
Communication Setup window. Applies only if a valid LAN or
Modem communication option is enabled.
Refer to Chapter 9 for more information.
RR Analysis Enters the RR Analysis Modality. Available only if the RRAN

option is enabled.
More Toggles between the first and second row of acquisition options.
Page 2
Next Patient Opens the patient entry window to allow you to enter or select a
new patient.
Speed Changes the speed of the waveform on the display and printout.
Change the speed also changes the speed the wiper bar moves
across the display.
Gain Changes the magnitude of the ECG signal on the display or in

the report. Measurement is in millimeter per millivolt (mm/mV).
Filter Eliminates noise in the waveform by restricting which

frequencies are included. Frequencies are measured in Hertz
(Hz).
More Toggles between the second and third row of acquisition options.
Page 3
Printer Leads Selects which leads to include in the printout.
Reanalyze Allows you to edit the global measurement and T-wave

dispersion. Available only if:
 the Audit Trail is disabled on the Basic Setup window,

 either measurement option (ME12 or MI12) is enabled, and
 the Reanalysis option is selected in the Resting ECG Setup
window.

Option Description
Laser Print Prints the ECG report to an external USB laser printer.
Main Menu Exits the Resting ECG function and return to the Main Menu.
Generating a Rhythm Report (Manual recording)

The Resting ECG mode allows you to generate Rhythm Reports, which
are printed reports only. They will not have computer-generated
interpretation or measurements, and they cannot be stored to internal
memory or transmitted. Use the following steps to generate a Rhythm
Report.
2. Verify the system is in Resting ECG mode.
If the system is not in the Resting ECG mode, press the Resting ECG
softkey at the Main Menu.
4. Adjust the Speed, Gain, and Low Pass Filter until the waveforms are
configured as desired.
5. If the patient has a pacemaker, press the Pace Enhance softkey.
6. Press the Leads key to scroll through all 12 leads.
For more information on display formats, refer to “Resting ECG

7. Press the More softkey.
8. Press the Printer Leads softkey to select the appropriate option.
For more information on the Printer Leads option, refer to “ECG

9. Press the Rhythm key to begin recording the ECG.
10. Press the Stop key to stop the ECG recording.
If you press the Rhythm key after pressing the Stop key, the new report
will either begin printing immediately on the current sheet of paper or
advance to a new page, depending on the setting of the Start rhythm
report on a new page field on the Resting ECG Setup window. Refer to
“Resting ECG Setup” on page 9-5 for details.

ECG Reanalysis
You can reanalyze ECGs if the following conditions have been met:
 The Audit Trail option is disabled on the Basic Setup window,

 Either the Measurement and 12SL Interpretation system option
(MI12) or the Measurement 12SL system option (ME12) is enabled,
and
 Reanalysis is selected on the Resting ECG Setup window.
Reanalysis allows you to modify the Global Measurements fiducial points

on acquired waveforms. Refer to the Marquette 12SL ECG Analysis
Program Physician’s Guide (416791-004) for additional information.
Reanalyzing an ECG
Use the following procedure to reanalyze a resting ECG.
For additional information, refer to “Reanalysis Layout” on page 5-10

and “Reanalysis Options” on page 5-11.
1. After acquiring an ECG, press More > More > Reanalyze.
For instructions on acquiring a resting ECG, refer to “Recording a

Resting ECG” on page 5-3.
2. Review the waveforms to determine the accuracy of the system-

selected fiducial points.
For a better view of individual waveforms, use the Leads key to

toggle through the waveforms. See “Reanalysis Layout” on page 5-10
for more information.
3. After you have analyzed the waveforms, use the following procedure
to adjust the fiducial points:
a. Press the Next softkey to toggle through the fiducial points.
The selected point changes size and is highlighted green.
b. When the correct point is selected, use the trimpad to adjust its
position.
c. To verify correct positioning, refer to the values in the

Measurement Legend in the lower left corner of the display.
For more information on the Measurement Legend, refer to

“Reanalysis Layout” on page 5-10.
d. Repeat step a through step c for each fiducial point to be

adjusted.
4. When you are done adjusting the fiducial points, do one of the
following:

 To discard your adjustments and start over, press the Restore

softkey.
The original readings are restored. Return to step 2 to start over.
 To save your adjustments, press the Save softkey.
The changes are saved
5. Repeat from step 2 to make adjustments in the other edit mode.
6. After all your changes have been made, press the Return softkey to
return to the original menu options.
Reanalysis Layout
Selecting the Reanalysis option after acquiring a resting ECG displays
the following screen. The screen’s key features are described in the
following table.
047A
Feature Description
A Waveforms A composite view of the ECG reading generated by

superimposing the median waveforms from all 12
leads.
Press the Leads key to toggle through the individual

waveforms. The selected waveform is brighter than the
others.

Feature Description
B Fiducial Points Each fiducial point is represented by a vertical line

through the composite waveforms.
Press the Next softkey to toggle through the fiducial

points. When a point is selected, it increases in size
and is highlighted green. A selected fiducial point can
be adjusted by pressing the left and right arrows on the
trimpad.
C Measurement The measurement, in milliseconds (ms), for the

Legend following:
 P Duration
 PR Interval
 QRS Duration
 QT Interval
As you adjust the fiducial points, these measurements
adjust accordingly.
Reanalysis Options
The following options are available when reanalyzing an ECG.
Option Description
Next Cycles through the following fiducial points on the superimposed

waveforms:
 P-onset
 P-offset
 QRS-onset
 QRS-offset
 T-offset
As it cycles through each point, the selected point is doubled in
size and highlighted green for ease of visibility.
Use the left and right arrows on the trimpad to move the
selected point. As you adjust points, the corresponding
measurements in the Measurement Legend adjust accordingly.
P Measurement Toggles the format of the P Duration and PR Interval

measurements in the Measurement Legend and toggles the
fiducial points from solid lines (certain) to dotted lines (uncertain).
Available only when the P-onset or P-offset fiducial points are

selected.

Option Description
Restore Returns all fiducial points to their original positions.
Use this option to undo any changes and begin over.
Save Applies the waveform marker changes to the ECG record. When
the ECG is next printed, it will be reanalyzed with the new
settings.
Return Exits the reanalysis function and returns to the Resting ECG
mode.
If you select this option before you press the Save softkey to
save your changes, you will lose your changes
Hookup Advisor
The Hookup Advisor is a visual indication of the quality of lead signals.
Monitoring it can help reduce or eliminate poor quality ECGs, saving
time and preventing the need to take additional ECGs.
046A
The Hookup Advisor is positioned in the upper right corner of the screen,
to the left of the heart rate. The following table describes each of the
indicator’s conditions.
Indicator Description
Red Indicates a lead-fail condition or extreme baseline shifts. A

corresponding message is displayed.
Yellow Indicates muscle artifact, power line interference, baseline wander, or

electrode noise. A corresponding message is displayed.
Green Indicates acceptable signal quality.

When a red or yellow indicator is lit, identify and correct the error before
proceeding with the ECG.
Hookup Advisor is enabled and configured in the Resting ECG Setup.

Refer to “Resting ECG Setup” on page 9-5 for more information.
Special Considerations
When recording ECGs, special considerations must be made for the
following situations:
 Recording ECGs of pacemaker patients

 Recording ECGs during defibrillation
Recording ECGs of Pacemaker Patients

Because of slow paper speed, pacer pulses cannot be displayed directly on
the ECG recording. For example, with a paper speed of 50 mm/s and a
pulse duration of only 0.5 ms, the width of the recorded pacer pulse
would be only 0.025 mm.
If Pulse Enhance is enabled, the recorder reduces the pulse amplitude

and expands its width to make pacer pulses easier to identify. The
system records the pulse with the correct polarity, a width of 5 ms, and
equal amplitude in all leads. Depending on the polarity of the pacer pulse
in leads I and II, the pacer pulse in lead III may be suppressed. The
following figure of an ECG recording with pacer pulses shows the
amplitude of the reverse current.
047A
WARNING
INCORRECT HR, NO HR ALARM — If several adverse
conditions exist at once, the possibility that the pacer pulses
are interpreted (and counted) as QRS complexes should be
considered. At the same time, however, QRS complexes
might be suppressed in certain situations. Therefore,
pacemaker patients should always be watched closely.

Recording ECGs during Defibrillation

This equipment is protected against the effects of cardiac defibrillator
discharge to allow the ECG trace to return after defibrillation, as
required by test standards.
The patient signal input is defibrillation-proof; it is not necessary to

remove the ECG electrodes before defibrillating the patient.
However, when using stainless steel or silver electrodes, the defibrillator

discharge current may cause the electrodes to retain a residual charge,
causing an electrode polarization or DC offset voltage. This will block
ECG signal acquisition for several minutes. If polarizing electrodes are
used, GE recommends that the leadwires be disconnected from the
patient before delivering the shock.
To prevent polarization, GE recommends the use of non-polarizing

disposable electrodes with defibrillation recover ratings as specified in
AAMI EC12 3.2.2.4 (MMS PN 9623-105 Silver MacTrodes, MMS spec
TP9623-003), which requires the polarization potential of an electrode
pair not exceed 100mV five seconds after a defibrillation discharge.
WARNING
EQUIPMENT DAMAGE — For patient safety, use only
the original GE patient cable. Before connecting the cable
to the device, check it for signs of mechanical damage. Do
not use a damaged cable.
WARNING
SHOCK HAZARD — During defibrillation, do not touch
the patient, the electrodes, or the leadwires.
Observe all defibrillator safety information.

6 Arrhythmia Mode
Recording

Arrhythmia Mode Recording
Introduction
The Arrhythmia mode is part of the basic MAC 800 system. It allows you
to manually generate an arrhythmia printout in a table format, an
episode format, or a summary format.
The interface of the Arrhythmia mode is identical to the interface for the
Resting ECG mode. For more information on the interface, refer to
“Introduction” on page 5-2. In addition to the same waveform options
(speed, gain, filter, pace enhance, and patient data) as the Resting ECG
mode, arrhythmia mode also offers an anti-drifting system (ADS) that
helps reduce baseline shift.
Arrhythmia Mode
This section describes the process for recording an arrhythmia report,
the waveform options, and the printing options.
Printing an Arrhythmia Report

Use the following steps to record an arrhythmia report.
2. From the MAC 800 Main Menu, press the Arrhythmia softkey
The Enter Patient Data window opens.
4. Adjust the gain, speed, filter, anti-drift system, and pacemaker

detection as necessary.
Refer to “Arrhythmia Options” on page 6-3 for details.
5. When the settings have been adjusted as required, press the Start
Recording softkey to begin the arrhythmia report.
6. After you have recorded an adequate amount of information, press

the Stop Recording softkey.
Two new options become available: Confirm Stop and Continue

Recording.
7. Do one of the following:
 If additional information needs to be recorded, press the

Continue Recording softkey.
This returns to the recording mode. Repeat from step 6.
 If you have determined enough information has been recorded,
press the Confirm Stop softkey.
Report options become available.

8. Select the type of Arrhythmia Report to print and press the

appropriate function key.
 To print the summary report, press the Print Summary softkey.

 To print the table report, press the Print Table softkey.
 To print episodes report, press the Print Episodes softkey.
Refer to “Printing Options” on page 6-5 for details.
9. Review the report as necessary.
For more information, refer to “Arrhythmia Codes” on page 6-5.
Arrhythmia Options
The MAC 800 provides several options for configuring an Arrhythmia
report. The options, presented as option keys across the bottom of the
display, are listed in the following table.
Option Description
Start/Stop Recording Starts and stops the arrhythmia reading.
Sweep Speed Changes the speed of the waveform on the display and printout.
Changing the speed also changes the speed the wiper bar
moves across the display.
Measurement is in millimeter per second (mm/s) and includes the

following options:
 25 mm/s
 50 mm/s
 12.5 mm/s - 5 mm/s
When the option includes two speeds (12.5 mm/s - 5 mm/s), the
first speed is for the display and the second speed is for the
printout.

Option Description
Gain Changes the magnitude of the ECG signal on the display or in

the report. Measurement is in millimeter per millivolt (mm/mV)
and includes the following options:
 5 mm/mV
 10 mm/mV
 20 mm/mV
 40 mm/mV
 2.5 mm/mV
 Automatic
NOTE
If Automatic is selected, the system calculates the best gain
based on the peak-to-peak amplitudes of all displayed leads
and the selected display format.
Filter Eliminates noise in the waveform by restricting which frequencies

are included. Frequencies are measured in Hertz (Hz) and
include the following options:
 20 Hz
 40 Hz
 100 Hz
 150 Hz
frequency. The smaller the frequency selected, the more signal is
filtered out. For example, a filter of 40 Hz displays only signals at
40 Hz or less; signals greater than 40 Hz will be ignored.
CAUTION
cleaner waveform, but selecting a frequency that is too low could
alter the waveform’s morphology, resulting in an inaccurate
reading.
ADS Toggles the anti-drift system (ADS) on and off. ADS helps reduce
baseline drift.
More Toggles through the softkey options.

Option Description
Main Menu Exits the Arrhythmia function and returns to the Main Menu.
Printing Options
When printing an arrhythmia report, you have the following options.
Option Description
Print Summary Prints a combined report that includes both the Table and
Episode formats.
Print Table Prints a breakdown of the recording in tabular format. The report
includes:
 the analysis duration in minutes and seconds,

 the artifact duration in minutes and seconds,
 a code for each event type recorded, and
 the number of each event type recorded.
For a description of the possible event codes, refer to
“Arrhythmia Codes” on page 6-5.
Print Episodes Prints a standard waveform report of the recorded events. The
signal from all recorded leads is printed, and each event is
marked with the corresponding arrhythmia code.
For a description of the possible event codes, refer to

“Arrhythmia Codes” on page 6-5
Arrhythmia Codes
The following table identifies the codes used on the arrhythmia reports
and the events they represent.
Code Arrhythmia Event
A Artifact
ASYSTO Asystole, limit value 3 s
CPLT Ventricular couplet (2 PVCs)
ESC Ventricular escape beat
L Learn phase
PAU1 Pause of 1 missed beat
PAU2 Pause of 2 missed beats

Code Arrhythmia Event
PCAP Pacemaker capture
PERR Pacemaker malfunction
PSVC Premature supraventricular contraction
PVC Premature ventricular contraction
QRSL Learned QRS complex
RUN Ventricular run (3 PVCs)
VBIG Ventricular bigeminy
VFIB Ventricular fibrillation/flutter
VTACH Ventricular tachycardia (>3 PVCs)

7 RR Analysis

RR Analysis
Introduction
RR Analysis is an optional mode of MAC 800 system. It detects hidden
patterns underlying the complex dynamic phenomena of heart rate
variability (HRV) and measures the cardiac RR intervals. Not available
in the U.S.
RR Analysis Mode
This section outlines the procedure for generating an RR Analysis report
and describes the available setup, waveform, and output options.
Printing an RR Analysis Report

Use the following steps to generate an RR Analysis report.
2. From the MAC 800 Main Menu, press the RR Analysis softkey.
You can also access RR Analysis from the Resting ECG mode after an
ECG has been acquired. For more information, refer to
“Post-Acquisition Options” on page 5-6.
3. Press the Patient Data softkey and enter the patient data as
described in Chapter 4.
4. Press the RR Analysis Setup softkey and adjust the setup options as
necessary.
Setup options include target, record lead, gain, speed, filter,

pacemaker detection, rhythm record, and RR table. Refer to “RR
Analysis Options” on page 7-3 for details.
5. Press the Save softkey to record your settings.
6. Press the Start Test softkey.
The device begins to acquire the ECG. The analysis target, acquired
beats, and acquired time are updated in real time on the screen.
7. While the ECG is being acquired, you can do any of the following:
 Change the sweep speed.

 Change the gain.
 Change the low pass filter.
 Toggle pace enhancement.
For more information on any of these options, refer to “Waveform

When the target is achieved, a preview of the summary results,

histogram, and trendgram is shown on the display.

RR Analysis
8. While reviewing the preview, do any of the following.
 To discard the reading and begin over, press the Return softkey
and repeat from step 6.
 To discard the reading and return to the Main Menu, press the
Main Menu softkey.
 To accept the reading and print the report on the thermal
printer, press the Print softkey.
 To accept the reading and export the results to a PDF file, press
the PDF Export softkey.
 To accept the reading and print the report on an external laser
printer, press the Laser Print softkey.
For more information on each option, refer to “Output Options” on
page 7-5.
RR Analysis Options
The following options are available before you begin an RR Analysis test.
Option Description
Start Test Starts the RR Analysis test.
RR Analysis Setup Configures the RR Analysis test. Refer to “RR Analysis Setup”
on page 7-5 for details.
Main Menu Exits the RR Analysis mode and returns to the Main Menu.
Waveform Options
The following options are available during the RR Analysis test.
Option Description
Stop Test Stops the RR Analysis test.
Sweep Speed Changes the speed of the waveform on the display. Changing
the waveform speed also changes the speed the wiper bar
moves across the display.
Measurement is in millimeter per second (mm/s) and includes

the following options:
 12.5mm/s
 25mm/s
 50mm/s

RR Analysis
Option Description
Gain Changes the magnitude of the ECG signal on the display.

Measurement is in millimeter per millivolt (mm/mV) and includes
the following options:
 2.5mm/mV
 5mm/mV
 10mm/mV
 20mm/mV
 40mm/mV
 Automatic
NOTE
If Automatic is selected, the system calculates the best
gain base on the peak-to-peak amplitudes of all displayed
leads and the selected display format.
Low Pass Filter Eliminates noise in the waveform by restricting which

frequencies are included. Frequencies are measured in Hertz
(Hz) and include the following options:
 20Hz
 40Hz
 100Hz
 150Hz
frequency. The smaller the frequency selected, the more signal
is filtered out. For example, a filter of 40Hz displays only signals
at 40Hz or less; signals greater than 40Hz will be ignored.
CAUTION
cleaner waveform, but selecting a frequency that is too low
could alter the waveform's morphology, resulting in an
inaccurate reading.
Pace Enhancement Improves the readability of pacemaker ECG. Options are On

and Off.

RR Analysis
Output Options
The following options are available after the RR Analysis test completes.
Option Description
Print Prints the RR Analysis Report on the thermal printer.
PDF Export Exports the RR Analysis Report to a PDF file.
Laser Print Prints the RR Analysis Report to an external laser printer.
Main Menu Exits the RR Analysis mode and returns to the Main Menu.
Return Returns to pre-test status.
RR Analysis Setup
The RR Analysis Setup function allows you to configure the RR Analysis
report, including:
 Target
 Record lead
 Waveform parameters
 Report options
To reach the RR Analysis Setup function from the MAC 800 Main Menu,
press RR Analysis > RR Analysis Setup.
The following table describes each available setting on the RR Analysis

Setup window.
Field Description
Target Selects the target of the test.
Record Lead Selects which rhythm lead will be displayed and stored.
Line Filter Enables/disables the line filter defined in Country Setup.

Refer to “Country Setup” on page 9-17 for more
information.
Pace Enhancement Improves the readability of pacemaker ECGs. Options are

On and Off.

RR Analysis
Field Description
Gain Sets the magnitude of the ECG signal. Measurement is in

millimeter per millivolt (mm/mV) and includes the following
options.
 2.5 mm/mV
 5 mm/mV
 10 mm/mV
 20 mm/mV
 40 mm/mV
 Automatic
The larger the selected measurement, the larger the

waveform. Only the appearance of the waveform changes;
signal strength is not affected.
NOTE
If Automatic is selected, the system calculates the
best gain based on the peak to peak amplitudes of all
displayed leads and the selected display format.
Sweep Speed Changes the speed of rhythm printing and the rate the
wiper bar moves across the display.
Measurement is in millimeter per second (mm/s) and

includes the following options.
 12.5mm/s
 25 mm/s
 50 mm/s
Low Pass Filter Sets the maximum frequency to include in the waveform.
Restricting frequencies can help eliminate noise in the
waveform. Frequencies are measured in Hertz (Hz) and
include the following options.
 20Hz
 40Hz
 100Hz
 150Hz
Selecting a frequency eliminates signals above that
frequency. For example, if you select 40, only signals that
have a frequency of 40 Hz or lower are included in the
waveform.

RR Analysis
Field Description
High Pass Filter Sets the minimum frequency to include in the waveform.
 0.04Hz
 0.08Hz
 0.16Hz
 0.31HZ
Selecting a frequency eliminates signals that fall below that

frequency. For example, if you select 0.16, only signals
that have a frequency of 0.16 Hz or higher are included in
the waveform.
Rhythm Record Enables/disables the printing of the rhythm lead waveform

on the report.
RR Table Enables/disables the printing of the RR table on the report.

RR Analysis

8 Managing Internal
Storage

Managing Internal Storage
Introduction
The File Manager provides an interface to the system’s optional internal
storage. It provides the tools to:
 import records from an external source,

 print the internal storage directory,
 search stored records,
 edit a record’s patient data,
 delete records,
 print records,
 transmit records to an external device, and
 export records to a secure digital card or shared directory.
Only resting ECGs can be saved to internal storage; arrhythmia and RR

analysis can only be printed.
Resting ECGs can be stored automatically or manually:
 To save resting ECG records automatically, set the Auto Store ECG
check box on the Resting ECG Settings window.
For more information, refer to “Resting ECG Setup” on page 9-5.
 To save resting ECG records manually, press the Save softkey after
the resting ECG has been acquired.
For more information, refer to “Post-Acquisition Options” on
page 5-6.
To enable internal storage, either the M100 Internal Storage for 100
ECGs option or the M300 Internal Storage for 300 ECGs must be
enabled.
For information on enabling the internal storage option, refer to “Options


Importing Records
In addition to saving ECGs recorded with the MAC 800 device, you can
also import ECG records to internal storage from the following sources:
 Secure Digital (SD) cards

 MUSE systems connected via serial port or modem
No additional set up is required to import from an SD card. However, you

must do the following to import data via serial port or modem:
 Purchase and activate the appropriate communications option.

For more information refer to “Options Setup” on page 9-23.
 Configure the system’s data communication settings.
For more information, refer to “Communication Setup” on page 9-13.
Use the following instructions to import a record into internal storage.
1. From the Main Menu, press the File Manager softkey.
The File Manager window opens.
2. Press the Import softkey.
The function keys change.
051A
3. Select the appropriate import source:
 To import ECGs from an SD card, insert the SD card and press

the SD Card softkey.
A list of the available ECGs on the card opens. Proceed to step 4.
 To import ECGs via serial port, press the Serial softkey.
The serial port opens. The device waits for the external device to
transmit records.
 To import ECGs via modem, press the Modem softkey.
The modem initializes. The device waits for the external device to
transmit records.
4. Select the records to be imported from the SD card.
5. When the correct records are selected, press the Import softkey.

The selected records are imported from the SD card into internal
storage.
NOTE
Imported records have a Sent status of Recv and cannot be edited,
transmitted, or exported in either Hilltop or XML format; however,
they can be exported in PDF format.
Printing the File Manager Directory

Use the following instructions to print the directory of ECGs stored in
internal memory.
2. Press the Print Directory softkey.
The directory prints on the MAC 800 writer.
Finding Records
The File Manager may have up to 300 records to manage, making it
difficult to find a specific record. To help you locate a record or a group of
records, use the following instructions.
2. Press the Search softkey.
The Enter Search Criteria window opens.

054A
3. Enter the search criteria.
4. Press the Search softkey.
The File Manager retrieves all the records that match the search
criteria.
5. To clear the search results, do one of the following:
 Press Main Menu > File Manager.

 Press Search > Return.
Editing Patient Data

Use the following instructions to edit a record’s patient data.
2. Press the Select softkey.
This enters the File Manager into select mode.
3. Use the trimpad to select the record to be edited.
NOTE
You cannot edit the patient data for records that were imported
to internal storage. Imported records have a Sent status of Recv.

4. Press the Edit softkey.
The Enter Patient Data window opens.
052A
5. Edit the information as appropriate.
For instructions on editing patient information, refer to Chapter 4.
6. When the information has been updated, press the Save softkey.
The updated information is saved, and you return to the File

Manager window.
Deleting Records
Use the following instructions to delete all records from internal storage.
2. Do one of the following.
 To delete select records, press the Select softkey and use the
trimpad to select the record(s) to be deleted.
 To delete all the records in storage, press the Select All softkey.

3. Press the Delete softkey.
A window opens and prompts you confirm that you want to delete the
selected record(s).
 To cancel the deletion, press No.

 To delete the record(s), press Yes.
Printing Records
The MAC 800 system supports printing to both the internal thermal
writer and to an external laser printer. Use the following instructions to
print records.
 To print select records, press the Select softkey and use the
trimpad to select the record(s) to be printed.
 To print all the records in storage, press the Select All softkey.
 To print to the internal thermal printer, press the Print softkey.

The selected records are printed on the MAC 800 writer.
 To print to an external laser printer, press the Laser Print
softkey.
The selected records are printed on the designated laser printer.
Transmitting Records
Use the following instructions to transmit records from internal storage
to an external device.
Before transmitting a record, you must do the following:
 Purchase and activate a communication option.

Refer to “Options Setup” on page 9-23 for more information.
 Configure data communications.
Refer to “Communication Setup” on page 9-13 for more information.

 Connect the MAC 800 unit to the communication device.

 To set up a LAN connection to a Cardiosoft system, see
“Connecting to a LAN” on page 2-11.
 To set up a LAN connection to a MUSE system, see the LAN
Option for MAC Series Installation and Troubleshooting Guide
(PN 2020299-025).
 To transmit select records, press the Select softkey and select the
record(s) to be transmitted.
NOTE
You cannot transmit records that were imported to internal
storage. Imported records have a Sent status of Recv.
 To transmit all the records in storage, press the Select All

softkey.
3. Press the Transmit softkey.
One of two things happens, depending on the number of locations

defined in Communications Setup.
 If only one location is defined, the files are transmitted to the

default location.
 If multiple locations are defined, a window listing the locations
opens. Select the correct location and press OK.
Exporting Records
You can export records from internal storage to a Secure Digital card or
to a shared directory in either an XML or PDF format. The maximum
number of records you can export in XML format is determined by which
storage option is enabled: if M100 is enabled, the maximum is 100; if
M300 is enabled, the maximum is 200. Records exported in PDF format
have no maximum limit.

NOTE
The SD card capacity and manufacturer determine data transfer
rates and storage space. This may affect the time required to read or
write to the SD card. It may also limit the number of records that can
be stored on the card. GE Healthcare recommends you use SD cards
with a capacity of 2GB or smaller and either supplied by GE
Healthcare or manufactured by SanDisk.
Setting Up Export Options

The requirements for setting up export differ depending on the export
method.
To export XML data to an SD card, no additional set up is required.
To export PDF files to an SD card, you must first enable the PDFC (PDF
Export) system option. Refer to “Options Setup” on page 9-23 for details.
To export either XML or PDF to a shared directory, you must do the

following:
 Purchase and activate the LAN Communications to Cardiosoft

(LANC) option.
Refer to “Options Setup” on page 9-23 for details.
 Define the shared directory settings on Communications Setup.
Refer to “Communication Setup” on page 9-13 for details.
Exporting Records
Once the necessary configurations are complete, use the following
instructions to export records from internal storage.
2. Select the record(s) to be exported.
 To export select records, press the Select softkey and use the
trimpad to select the records to be exported.
NOTE
Records imported to internal storage cannot be exported in
Hilltop or XML formats; however, they can be exported in
PDF format. Imported records have a Sent status of Recv.
 To export all records in storage, press the Select All softkey.

3. Press More > Export.
The softkeys change. Depending on which options have been

activated, the softkeys may include Hilltop XML, PDF, and Return.
4. To export to an SD card, insert the card into the SD Card slot.
The card must have sufficient free space for the selected records and
must not be write protected.
NOTE
If you do not enter the SD card into the MAC 800 SD Card slot,
you will receive a warning (SD-Card is not present) when you
attempt to export data to the card. Refer to “SD Card Not
Present” on page A-4 for instructions on how to proceed.
5. Press the appropriate softkey.
 To export in XML format, press Hilltop XML.

 To export in PDF format, press PDF.
 To return to the previous set of softkeys, press Return.
If you press Hilltop XML or PDF, one of two things happens,
depending on your system configuration:
 If a shared directory has been configured, the Select Export

Destination window opens.
Skip to step 6.
 If a shared directory has not been configured, the records are
automatically exported in the selected format to the SD Card.
When the export is complete, one of two things happens
depending on the selected format:
 For the Hilltop XML format, the screen clears and the
softkeys change.
 For the PDF format, a summary window opens with the
number of records that exported successfully and the number
that failed to export. Press OK to close the summary window.
You can now select additional records to export. Return to step 2.
6. In the Select Export Destination window, select the appropriate

export destination:
 To export to an SD card, select SD Card.

 To export to the shared directory, select Shared Directory.

NOTE
When exporting to a shared directory, the MAC 800 device
logs on to the directory with the user name and password
defined on the Communications Setup window. If either of
those values are incorrect, you will receive an error message.
Correct the user name and password on the Communications
Setup window and repeat the export process.
7. Press OK.
The selected records are exported to the selected destination. When

the export is complete, one of two things happens depending on the
selected format:
 For the Hilltop XML format, the screen clears and the softkeys
change.
 For the PDF format, a summary window opens with the number
of records that exported successfully and the number that failed
to export. Press OK to close the summary window.
You can now select additional records to export. Return to step 2.
PDF File Naming Convention

To help identify the exported PDF files, they are automatically named
with the following descriptive components:
product_version_serial_ECGmode_cartID_creationdata.pdf
For example:
GEMAC800_1.0_SDS07410016WP_resting_1_2007-11-22T17-56-32.pdf
The following table identifies each component in the example:
Value Component/Description
GEMAC800 Product name. This will always be GEMAC800.
1.0 Software version. This will vary depending on the software

version installed.
SDS07410016WP Unit serial number. This will vary from unit to unit.
resting ECG mode. This will be either resting (Resting ECG mode)
or rrana (RR Analysis mode).

Value Component/Description
1 Cart ID. This will vary from unit to unit.
2007-11-22T17-56-32 Creation data. This consists of the following

subcomponents:
 2007 - Year the PDF was written.

 11 - Month the PDF was written.
 22 - Date the PDF was written.
 T - Indicates the following numbers are time.
 17 - Hour, in 24 hour format, the PDF was written.
 56 - Minute the PDF was written.
 32 - Second the PDF was written.

9 System Configuration

System Configuration
Introduction
System Configuration provides access to functions that allow you to
customize the MAC 800 settings and to utilities to help manage those
settings. This chapter describes the settings managed by each function
and the process followed by each utility.
CAUTION
POTENTIAL DATA LOSS — After making configuration
changes, you MUST return to the MAC 800 Main Menu to
ensure the changes are saved.
Setup Functions
Setup functions fall into the following categories:
 Basic system settings

 Resting ECG settings
 Arrhythmia settings
 Communication settings
 Country settings
 Patient settings
 User settings
 Options
 Service settings
 Date and time
Depending on which system options have been activated, some of these

functions may not be available on your device.
Basic Setup
The Basic Setup function allows you to define the following information:
 Institutional identification
 Default physicians
 System settings
 System security
 Time servers
NOTE
Physicians must be added in User Setup before they can be picked as
default physicians. For more information, refer to “User Setup” on
page 9-21.

To reach the Basic Setup from the MAC 800 Main Menu, press System
Configuration > Basic Setup.
The following table describes each setting available on Basic Setup.
Field Comment
Page 1
Name The name of the institution.
Street The street address of the institution.
City The city where the institution is located.
Ordering Physician The physician who ordered the ECG. Defaults on any
patient records created on the device.
Referring Physician The physician who referred the patient. Defaults on any
Attending Physician The physician who supervised the ECG. Defaults on any
Technician The technician who conducted the ECG. Defaults on any

Location Location ID where the device is located. Defaults on any

Site # Site number where the device is located. Defaults on any

Required to store ECG reports on a cardiology information

system, such as the MUSE™ system.
Cart # Unique cart number of the device. Defaults on any patient

records created on the device.
Test Patient (temporary) Enables/disables simulated ECGs. When enabled,

simulated waveforms are generated in the resting,
arrhythmia, or RR Analysis ECG functions. This is useful
for demonstration, training, or testing purposes.
NOTE
This setting clears when the unit is reset.
Page 2
Power up mode Determines which screen will appear when the device is
powered on. Available options are:
 Resting ECG
 Arrhythmia
 Main Menu
Resting ECG is the default value.

Field Comment
Display Colors Determines the appearance the ECG display. Select a

color combination that is legible for you.
ECG Grid on Display Determines whether a grid is displayed behind the

waveforms. A grid may make reading the ECG easier.
Default is on.
Anti-Aliasing of ECG Determines whether anti-aliasing will be applied to

Waveforms waveforms to reduce distortion caused by the video
display. Default is on.
Auto Standby Determines whether the device will automatically enter

standby mode if it is inactive for a predefined time limit.
This helps reduce power consumption and increases the
life of the device. See also Auto Standby Time.
Auto Standby Time Identifies the amount of time, in minutes, that the device
(1-255 min) can remain inactive before it enters standby mode. Used
by the Auto Standby field.
Page 3
High Security Mode Enables/disables high security mode. It can be activated

only if at least one user with Edit Users and Edit Setup
privileges has been configured with a password.
When high security mode is enabled, users are prompted

to enter an ID and password when logging on to the
device. Each user will need to be added to User Setup. For
more information, refer to “User Setup” on page 9-21.
Audit Trail Determines whether the device will create an audit trail of
activity. Available only if High Security Mode is enabled
and the CFRA audit trail option is activated. For
information on activating the CFRA option, refer to
“Options Setup” on page 9-23.
Auto Logoff Determines whether the device will automatically log the
user off after a predefined period of inactivity.
See also Auto Logoff Time. Available only if High Security

Mode is enabled.
Auto Logoff Time Determines the length of inactivity, in minutes, before the
(1-255 min) device will log off the user. Available only if High Security
Mode is enabled.
Automatically synchronize Enables/disables automatic synchronization with an

with Time Server external time server either on the institution’s network or
the Internet. A LAN option must be activated to set this
option.

Field Comment
Time Server Name Identifies the server with which the device will synchronize
its time. This can be a server on the institution’s network or
on the Internet. Contact your server administrator for this
information.
Last synchronization at Display-only field that identifies when the last

synchronization occurred.
Last synchronized from Display-only field that identifies where the last
Time Server synchronization occurred.
Resting ECG Setup

The Resting ECG Setup option allows you to define:
 Lead usage
 Analysis options
 Lead sequence
 Report options
 Storage options (if the internal storage option is activated)
 Transmission options (if a communications option is activated)
To reach the Resting ECG Setup from the MAC 800 Main Menu, press
System Configuration > Resting ECG Setup.
The following table describes each setting available on the Resting ECG
Setup.

Field Comment
Page 1
Gain [mm/mV] Sets the magnitude of the ECG signal. Measurement is in

millimeter per millivolt and includes the following options.
 2.5
 5
 10
 20
 40
 Automatic
The larger the selected measurement, the larger the

waveform. Only the appearance of the waveform changes;
signal strength is not affected.
NOTE
If Automatic is selected, the system calculates the
best gain based on the peak-to-peak amplitudes of all
displayed leads and the selected display format.
Speed [mm/s] Changes the speed of rhythm printing and that the wiper
bar moves across the display.
Measurement is in millimeter per second (mm/s) and

includes the following options.
 5 (rhythm) / 12.5 (display)

 25
 50
Low Pass Filter [Hz] Sets the maximum frequency to include in the waveform.
 20
 40
 100
 150
Selecting a frequency eliminates signals above that

frequency. For example, if you select 40, only signals that
have a frequency of 40 Hz or lower are included in the
waveform.

Field Comment
High Pass Filter [Hz] Sets the minimum frequency to include in the waveform.
 0.04
 0.08
 0.16
 0.31
Selecting a frequency eliminates signals that fall below that

frequency. For example, if you select 0.16, only signals
that have a frequency of 0.16 Hz or higher are included in
the waveform.
Line Filter Enables/disables the line filter defined in Country Setup.

Refer to “Country Setup” on page 9-17 for more
information.
6 leads: 1x6 Enables/disables a display option that shows one six-

waveform column.
6 leads: 2x3 Enables/disables a display option that shows two three-

waveform columns.
12 leads: 2x6 Enables/disables a display option that shows two six-

waveform columns. Available only if the R12L system
option is enabled.
12 leads: 4x3 Enables/disables a display option that shows four three-

waveform columns. Available only if the R12L system
option is enabled.
Display Format Selects the display format of the resting ECG. Default
value is 3 leads: 1x3. Other values depend on which of the
previous four fields are set.
Display Lead Group Determines which group of leads is displayed. The

available values depends on which Display Format is
selected. For example, if 3 Leads: 1x3 is selected, the
available values are:
 3 rhythm leads
 1st group
 2nd group
 3rd group
 4th group
If either of the 12-lead display formats is selected, this field

is not available, since all 12 leads are displayed.

Field Comment
Page 2
Printer Leads Identifies the default set of leads used for printing. The
values are:
 First 6
 Second 6
 Rhythm 6
Start rhythm report on new Determines whether the rhythm report should begin on a
page its own page.
Pace Enhancement Increases the readability of pacemaker ECG either by

augmenting small pace pulses or by truncating large pace
pulses. If enabled, pace enhance is done in two steps: (1)
Add a marker (1.5mV amplitude, 6 ms duration) to the
electrode signal. (2) Limit the sum to 0.5mV in the lead
signal.
Hookup Advisor Enables/disables the Hookup Advisor option, which

visually indicates the quality of lead signals. For more
information, refer to “Hookup Advisor” on page 5-12.
Preview before Analysis Determines waveform preview options. Values include:
 No
Waveforms are never previewed.
 Always
Waveforms are always previewed.
 Yellow electrodes
Waveforms are previewed when the Hookup Advisor
indicates a yellow or red electrode.
 Red electrodes
Waveforms are previewed when the Hookup Advisor
indicates a red electrode.
For additional information, refer to “Hookup Advisor” on
page 5-12.
ECG Acquisition Determines the ECG acquisition mode. Values include:
 Pre-Acquisition
Uses the last 10 seconds of ECG data already stored
in the system.
 Post Acquisition
Acquires 10 new seconds of ECG data after pressing
the ECG hardkey.

Field Comment
Reanalysis Enables/disables the reanalysis feature, which allows you

to adjust the following ECG measurements:
 P Duration
 PR Interval
 QRS Duration
 QT Interval
Available only if Audit Trail is disabled and either the ME12
or MI12 option is activated. For more information on
activating options, refer to “Options Setup” on page 9-23.
For more information on the reanalysis feature, refer to

“ECG Reanalysis” on page 5-9.
QTC Calculation Determines which formula will be used to correct QT

calculations. Options are:
 Bazett
QTc = QT HR
--------
60
 Framingham
QTc = QT + 154  1 – -------

60-
 HR
 Fridericia
HR-
QTc = QT 3 -------
60
In all formulas, HR = Heart Rate. Available only if the ME12
or MI12 option is activated.
Screening Criteria Enables/disables the inclusion of the screen criteria. This

setting is available only if the MI12 option is activated. It is
disabled by default.
Suppress normal statement Enables/disables the inclusion of the normal statement.

This setting is available only if the MI12 option is activated.
Suppress abnormal / Enables/disables the inclusion of the abnormal/borderline

borderline statements. This setting is available only if the MI12 option
is activated.
Suppress all statements Enables/disables the inclusion of all statements. This

setting is available only if the MI12 option is activated.

Field Comment
Suppress reason statement Enables/disables the inclusion of reason statements. This

setting is available only if the Screening Criteria field is
enabled. It is enabled by default.
NOTE
Reason statements are not yet available for all
languages.
ACI-TIPI Enables/disables the inclusion of the ACI-TIPI (Acute

Cardiac Ischemia Time Insensitive Predictive Instrument)
statement and enables the Chest Pain field on the patient
information window.
To include ACI-TIPI statements, the following conditions

must be met:
 MI12 or ME12 system option is activated

 TIPI system option is activated
 ACI-TIPI must be enabled
 10s ECG Report Format must be enabled
 Print interpretation must be enabled
 Patient data must include: gender, date of birth, and
chest pain indication.
 Patient cannot be a pediatric patient (15 years or
younger), as calculated from the date of birth.
For additional information, refer to the ACI-TIPI Physician’s
Guide (2002197-001).
Sample Rate Determines the report frequency. Options are 500 Hz or

1000 Hz. 1000 HZ is supported only for XML output.
Page 3
Lead Sequence Determines the lead sequence to use. Values are:
 Standard
 Cabrera
 NEHB
 SEQ4
SEQ4 allows you configure a custom 12-lead sequence

using the following fields. If either 12SL option (ME12 or
MI12) is activated, leads I (-I), II (-II), V1, V2, V3, V4, V5,
and V6 must be selected for a correct 12SL analysis.
Sequence Name Set the display name for a custom lead sequence.
Available only if SEQ4 is selected for the Lead Sequence.
1–12 Lead Twelve fields that allow you to define the sequence in
which the leads will appear. Available only if SEQ4 is
selected for the Lead Sequence.

Field Comment
1–12 Label Twelve fields that allow you to define the labels that will
appear/print for the corresponding leads. Available only if
SEQ4 is selected for the Lead Sequence.
1–6 Rhythm Leads Six fields that allow you to define the rhythm leads and
their sequence. You can select the rhythm leads for all four
lead sequences.
Page 4
10s ECG Report Format Determines how the 10s ECG report will print on the
internal writer. If no format is selected, the report will not
print.
Detailed Results Report Determines how the Detailed Results report will print. If no
Format format is selected, the report will not print.
Report Copies Determines how many copies of the selected report will
print.
Print Interpretation Determines whether ECG interpretation will print on the

report. Available only if the MI12 option is activated. For
more information, refer to “Options Setup” on page 9-23.
Auto Store ECG Determines whether the ECG will automatically be stored
on the internal storage. Available only if the M100 or M300
internal storage option is activated. For more information,
refer to “Options Setup” on page 9-23.
File Manager Sort By Determines the field by which the File Manager will sort
records in internal storage. Available only if the M100 or
M300 internal storage option is activated.
Auto Transmit ECG Determines whether the ECG will automatically be

transmitted to an external device. Available only if one of
the communications options is activated.
For more information, refer to “Options Setup” on

page 9-23.
Delete after Transmission Determines whether the ECG will be deleted from internal
storage after it is transmitted to an external device.
Available only if one of the communications options is
activated.

page 9-23.
Print Transmission Log Determines whether the transmission log prints after an
ECG is transmitted from File Manager to an external
device. Available only if one of the communications options
is activated.

page 9-23.

Field Comment
Page 5
10s ECG Report Format Determines how the 10s ECG report will print on an
external laser printer. If no format is selected, the report will
not print.
Report Copies Determines how many copies of the 10s ECG report will
print on an external laster printer. Valid values range from 0
to 5.
Paper Size Determines the page size of the report when it prints on a
laser printer. Valid values are A4 and Letter.
Print Grids Determines whether the grid will print on the report when it
prints on a laser printer.
10s ECG Report Format Determines how the 10s ECG report will print to a PDF file.
If no format is selected, the report will not print.
Arrhythmia Setup
The Arrhythmia Setup function allows you to define:
 Lead usage
 Analysis options
 Lead sequence
 Report options
To reach the Arrhythmia Setup from the MAC 800 Main Menu, press
System Configuration > Arrhythmia Setup.
Most of the fields on the Arrhythmia Setup windows are the same as
those on the Resting ECG Setup. The following table lists the arrhythmia
settings that are unique or differ from the resting ECG. For all other
fields, refer to “Resting ECG Setup” on page 9-5.
Field Comment
Page 1
ADS Enables/disables the Anti-Drift System, which helps reduce

baseline shift. In Arrhythmia mode, this setting is always
available.
Page 2
Rhythm Printing Determines whether the rhythm report will start

automatically when recording starts.

Field Comment
Arrhythmia Event Printing Selects which arrhythmia events will print. Options are:
 All events
 Unequal events
 No event printing
Episodes Printout in Determines how arrhythmia events will print. Options are:
Summary Report
 Chronological order
 Priority order
 Only episodes with ventricular events
 No episodes
Page 3
Lead Sequence Determines the lead sequence to use. Arrhythmia Setup

includes the following options in addition to the four options
available in the Resting ECG Setup:
 STD_C
 STD_RED
 STD_LI
 CABR_LI
 NEHB_6
 HIGH_C
Communication Setup
The Communication Setup function allows you to define:
 Basic communication settings

 Shared directory settings
 Destination location settings
 Modem settings (if a modem option is activated)
 LAN settings (if a LAN option is activated)
To reach the Communication Setup from the MAC 800 Main Menu, press
System Configuration > More > Communication Setup.
The following table describes the settings on Communication Setup.
Field Comment
Page 1
Default Location Determines which of the four available communication

locations will be the default. The locations are defined on
page 2 of Communication Setup.

Field Comment
Export XML Determines whether ECG records will be transmitted as

XML. If set, ECG records exported to SD card will be
stored in both XML and Hilltop formats. If not set, ECG
records exported to SD card will be stored only in Hilltop.
Serial Baud Rate Determines the speed at which data will be transmitted
across the serial communications port.
Allow Export Using Shared Determines whether ECG records can be exported to a
Directory shared network drive. Available only if the LAN
Communications to Cardiosoft option (LANC) has been
activated.
If this field is checked, the following five fields become

available.
Share Name Identifies the name of the shared network drive. It must be
the share’s name; IP addresses are not supported.
Maximum of 256 characters.
Available only if the Allow Export Using Shared Directory

field is checked.
Username Identifies the user name that the MAC 800 system will use
to log on to the shared directory. The user must be set up
on the domain with the appropriate permissions to access
the shared directory. Maximum of 30 characters.

field is checked.
Password Identifies the password that the MAC 800 system will use
to log on to the shared directory. Numeric only. Maximum
of 30 characters.

field is checked.
Confirm Re-enter the password in this field to confirm that the

password was typed correctly.

field is checked.
Domain Identifies the user’s domain. Maximum of 30 characters.

field is checked.
Page 2
Location Identifies the name of a communication location that will

receive the transmission from the MAC 800 system. Up to
four locations can be defined.

Field Comment
Device Identifies the type of device to be used to transmit data to

the location. Options are:
 Serial
 Modem
 LAN
Modem and LAN will be available only if the corresponding

option has been activated.
This field becomes active only after a corresponding

location has been entered.
Phone Number Identifies the location’s phone number. Available only if the
selected device is Modem.
Protocol Determines the protocol to be used to communicate with

the device. Options are:
 A5
 CSI
Select CSI for MUSE connections and A5 for Cardiosoft

connections.
Page 3
Dialing Method Determines whether the system will use a tone or pulse to
dial.
PIN Dialing Identifies whether a personal identification number (PIN) is

required to dial out. If this field is checked, the following
three fields need to be completed.
Delay Determines how long, in seconds, the system should

pause between dialing the Service Provider Number and
the PIN Number and between dialing the PIN Number and
the Outside Line.
Service Provider Number Identifies the service provider’s access telephone number.
PIN Number Identifies the personal identification number to enter.
Outside Line Identifies any access numbers that must be dialed to reach
an outside line.
Manual Dialing Determines whether the system will automatically dial. If

this field is checked, the connection must be made
manually. If this field is cleared, the system automatically
dials and you must complete the Dialing Method, Dialtone
Required, and PIN Dialing fields.

Field Comment
Page 4
Cardiograph Device Name Identifies the name that identifies the MAC 800 unit on the
network. By default, the value is set to
GE_<serial number>. A valid network device name
contains between 1 and 20 alphanumeric and underscore
characters. The first character must be a letter.
This field is available only if a LAN option has been

activated.
Serial/IP Redirector Listen Identifies the port the device should listen to for incoming
Port Serial/IP connections. These communications must match
the values defined on the transmitting MUSE system.
Obtain an IP address Determines whether the MAC 800 device will automatically
automatically (DHCP) receive an IP address from the network.
If this box is checked and LAN communication to a MUSE

system is enabled, the DHCP server must be configured to
reserve a static IP address for the MAC 800 unit. Contact
your network administrator for assistance.
If this field is checked, the IP Address, Netmask, and

Gateway fields are display-only. If this field is cleared, you
must complete those fields.
IP Address Identifies the IP address of the MAC 800 device. If the

Obtain an IP address automatically (DHCP) field is
cleared, you must define a unique IP address.
Netmask Identifies the netmask of the MAC 800 device. If the Obtain
an IP address automatically (DHCP) field is cleared, you
must define a netmask.
Gateway Identifies the IP address of the gateway to be used by the

MAC 800 device. If the Obtain an IP address automatically
(DHCP) field is cleared, you must enter the gateway’s IP
address.
Obtain DNS service Determines whether the MAC 800 device will automatically
address automatically obtain a DNS (Domain Name Server) IP address. If this
(DHCP) field is checked, the following two fields are display-only. If
this field is cleared, you must define the IP address of the
DNS servers to use.
Preferred DNS Server Identifies the IP address of the primary DNS server used to
resolve Internet domain names.
Alternate DNS Server Identifies the IP address of the secondary DNS server
used to resolve Internet domain names.

Country Setup
The Country Setup function allows you to define:
 System language
 Date and time formats
 Measurement units
 Line filter
 Lead label
To reach the Country Setup from the MAC 800 Main Menu, press System
Configuration > More > Country Setup.
The following table identifies the settings on Country Setup.
Field Comments
Language Determines the language used by the interface and

reports.
Date Format Determines the format in which dates are displayed.

Options are:
 DD.MM.YYYY
 MM/DD/YYYY
 YYYY-MM-DD
Time Format Determines whether the system will use a 12-hour or a

24-hour format.
Height/Weight Unit Determines whether the system will use metric

measurements (cm, kg) or English measurements (in, lb)
for patient weight and height.
Blood Pressure Unit Determines whether blood pressure will be measured in

millimeters of mercury (mmHg) or kilopascals (kPa).
Line Filter Determines the frequency of the line filter. Options are
50 Hz and 60 Hz.
Lead Label Determines whether the system will label leads using the
standards of the International Electrotechnical Commission
(IEC) or the American Heart Association (AHA).

Patient Setup
The Patient Setup function allows you to define the:
 Available and required patient information

 Available test information
 Available clinical trial information
Only if the CTDG CT Data Guard option is activated.
 Magnetic card reader
For complete information, refer to Appendix C.
 Barcode reader settings
Only if the BCRD USB Barcode Reader option is activated
To access Patient Setup from the MAC 800 Main Menu, press System
Configuration > More > Patient Setup.
The following table identifies the settings on Patient Setup.
Field Comment
Patient Information Setup Window
Patient ID Determines whether the patient ID is required. On reports,

it will be labelled ID.
Secondary ID Determines whether a secondary patient ID will be

available when entering patient data and whether it is
required. It can only be required if it is first enabled. On
reports, it will be labelled ID 2.
Last Name Determines whether the patient’s last name will be

required. It can only be required if it is first enabled.
First Name Determines whether the patient’s first name will be

required. It can only be required if it is first enabled.
Kanji Name Determines whether the Kanji name will be available when
entering patient data.
Date of Birth Determines whether date of birth will be available when

Age Determines whether age will be available when entering

patient data.
Height Determines whether height will be available when entering

patient data.
Weight Determines whether weight will be available when entering

patient data.

Field Comment
Gender Determines whether gender will be available when

Race Determines whether race will be available when entering

patient data.
Phone Number Determines whether phone number will be available when

Pacemaker Determines whether pacemaker will be available when

Enable Patient ID Check Determines whether additional checks will be performed to

ensure that the patient ID meets the requirements of the
national patient ID used in Scandinavian countries. If this
field is set, you must select the appropriate Patient ID
Type.
Patient ID Type Available only in the Enable Patient ID Check field is set.
Determines which type of ID will be used and, therefore,
which checks to perform. Options are:
 Swedish Patient ID
 Danish Patient ID
 Norwegian Patient ID
When a patient ID is entered, the system will verify its

format, extract the patient’s gender and date of birth, and
populate those fields if they have been enabled.
Patient ID Length (3-30) Defines the maximum length of the patient ID within the
range of 3 to 30 characters.
Available only if the Enable Patient ID Check field is

cleared.
Sort Patient List by Determines the field by which the patient list is sorted.
Options are:
 Patient ID
 Secondary ID
 Patient Name
Test Information Window
Systolic BP Determines whether systolic blood pressure will be

available when entering test information.
Diastolic BP Determines whether diastolic blood pressure will be

Location Determines whether location will be available when

entering test information.

Field Comment
Room Determines whether room will be available when entering

test information.
Order Number Determines whether order number will be available when

Indication Determines whether indication will be available when

Ordering Physician Determines whether the ordering physician will be

Referring Physician Determines whether referring physician will be available

when entering test information.
Attending Physician Determines whether attending physician will be available

when entering test information.
Technician Determines whether technician will be available when

entering test information and whether it will be required. It
can be required only if it has been enabled.
Medications (0-3) Determines the number of medications that can be entered

into the test information window.
Extra Questions… Opens the Extra Questions window, which allows you to
define up to four custom fields. Each field consists of a
Prompt and a Type. The Prompt can be up to 10
characters. The Type can be any of the following:
 Alphanumeric
 Numeric
 Yes/No/Unknown
Clinical Trial Setup Window
Visit Number Determines whether visit number will be available when

entering clinical trial information.
Visit Type Determines whether visit type will be available when

Dose Type Determines whether Dose Type will be available when

entering clinical trial information. If this field is set, use the
Dose List… button to define the types of doses that will
available when entering clinical trial information.
Investigator ID Determines whether investigator ID will be available when

Project Code Identifies the Project ID that will appear when entering
clinical trial information.
Trial ID Identifies the trial ID that will appear when entering clinical
trial information.

Field Comment
Extra Questions… Opens the Extra Questions window, which allows you to
define up to five custom clinical test fields. Each field
consists of a Prompt and a Type. The Prompt can be up to
10 characters. The Type can be any of the following:
 Alphanumeric
 Numeric
 Yes/No/Unknown
Dose List… Opens the Dose List… window, which allows you to define
the dose types that will be available when entering clinical
trial information. Doses are plain text up to 32
alphanumeric characters.
Barcode Scanner or Magnetic Card Reader Setup
Peripheral Device Determines whether the unit will be connected to a

Selection magnetic card reader, an optional barcode scanner, or no
peripheral device at all.
Auto Configure Automatically configures the barcode reader. When you

click this link, you will be prompted to scan a configuration
barcode created by the site’s IT department. For more
information on creating the barcodes, refer to Appendix B.
Available only when Barcode Scanner is select in

Peripheral Device Selection.
Total number of bytes Identifies the total number of bytes on the barcode or
magnetic strip.
Offset Identifies the position of the initial character of the

corresponding field.
Length Identifies the number of characters for the corresponding

field.
User Setup
The User Setup function allows you to define:
 User names
 User identification
 User roles
 User privileges
Users entered in setup can be selected for system defaults and patient
information. If High Security Mode is enabled, anyone who will use the
MAC 800 device must be set up as a user with a user ID, a password, and
privileges to be able to log on to the device. For more information on
setting system defaults and enabling High Security Mode, see “Basic

To reach User Setup from the MAC 800 Main Menu, press System
Configuration > More > User Setup.
When you run User Setup, the Edit User Lists window opens to offer four
choices:
 Ordering Physicians
 Referring Physicians
 Attending Physicians
 Technicians
When you select one of these roles, a list of existing users with that role
opens. You can now add, edit, and delete users.
The following table identifies the settings on User Setup.
Field Comment
Last Name Identifies the user’s surname. Required. 30 alphanumeric

characters.
First Name Identifies the user’s given name. Optional. 20

alphanumeric characters.
User ID Defines a unique ID for the user. If High Security Mode is

enabled, the user will need to enter this ID to log on to the
device. Required. 30 alphanumeric characters.
MUSE ID Defines the ID with which the user logs onto the MUSE
system. Used if reports from this system will be transmitted
to a MUSE system.
Ordering Determines whether the user fills the role of ordering

physician. If this is the role that was selected on the Edit
User List window, this field will be checked by default.
Multiple roles may be selected, but at least one role must
be selected.
Referring Determines whether the user fills the role of referring

be selected.
Attending Determines whether the user fills the role of attending

be selected.
Technician Determines whether the user fills the role of technician. If

this is the role that was selected on the Edit User List
window, this field will be checked by default. Multiple roles
may be selected, but at least one role must be selected.

Field Comment
Password Defines the password the user must enter along with the
User ID to log on to the device if High Security Mode is
enabled. Numeric only. Must be between 6 and 30
characters.
Retype Password Confirms the password was entered correctly.
Edit Setup Enables/disables the user’s ability to edit system setup

information.
Edit Date and Time Enables/disables the user’s ability to edit system date and
time.
Edit Users Enables/disables the user’s ability to edit user information.
Edit Record Enables/disables the user’s ability to edit ECG records.
Delete Record Enables/disables the user’s ability to delete ECG records.
Transmit Records Enables/disables the user’s ability to transmit ECG

records.
Options Setup
The Options Setup function allows you to activate options by entering
Option Codes, which are generated for a specific serial number and can
only be used to activate options on the device with that serial number.
All purchased options will be activated when the device ships. However,
if you purchase a new option or re-activate an option, use the following
instructions.
1. From the Main Menu, press System Configuration > More > More >
Options Setup.
2. Type the 12-digit activation code in the Option Code field.
You can find activation codes for purchased options on the Active
Code Summary Sheet provided with the device or with additional
purchased options.
3. Press the Enter key
The Option Activated message appears at the bottom of the window.
4. Repeat step 2 through step 3 for any additional options to activate.
5. Press the Save softkey to save the configuration options.
The following table identifies the available options. You will be given an
activation code for each purchased option.

Code Item Number Name
CTDG 2037986-001 CT Data Guard
R12L 2037986-002 12 Lead Display for Resting ECG. Always active.
ME12 2037986-003 12SL Measurement
MI12 2037986-004 12SL Measurement and Interpretation
M100 2037986-005 Storage for 100 ECGs
M300 2037986-015 Storage for 300 ECGs
LANC 2037986-006 LAN Communication to Cardiosoft
LANM 2037986-007 LAN Communication to MUSE
MODC 2037986-008 Modem or serial communication to Cardiosoft
MODM 2037986-009 Modem or serial communication to MUSE
CFRA 2037986-010 21 CFR Part 11 Audit Trail
BCRD 2037986-011 USB Barcode Reader
TIPI 2037986-012 ACI-TIPI
RRAN 2037986-013 RR Analysis
PDFC 2037986-014 PDF Export
Service Setup
The Service Setup option allows service personnel to configure the
following:
 Device settings
 Event log
 System diagnostics
See the MAC 800 Service Manual for details.
Date/Time Setup
The Date/Time Setup function allows you to configure the MAC 800
system’s date and time settings.
To reach Date/Time Setup from the MAC 800 Main Menu, press System
Configuration > More > More > More > Date/Time Setup.
The following table identifies the settings on Date/Time Setup.

Field Comment
Date Sets the current system date. The format depends on the date
format selected on Country Setup. See “Country Setup” on
page 9-17.
Time Sets the current system time. If the Automatically Synchronize with
Time Server field is set on Basic Setup, any changes made to the
time will be overwritten during the next synchronization. For more
information, refer to “Basic Setup” on page 9-2.
Time Zone Identifies the time zone in which the device is located. Available
only if Automatically synchronize with Time Server is enabled in
Basic Setup. See “Basic Setup” on page 9-2.
Adjust clock for Determines whether the system will automatically adjust the
daylight savings system time for daylight savings time. Available only if
time Automatically synchronize with Time Server is enabled in Basic
Setup. Refer to “Basic Setup” on page 9-2 for more information.
Setup Utilities
The setup utilities available in System Configuration allow you to print,
switch, export, and import system settings and export the audit trail.
Print Setup Report

The Print Setup Report utility prints a report of individual settings or the
complete system settings. You may use the report to verify that all MAC
800 devices are configured identically or to reference if you need to
reconfigure a device.
Use the following instructions to print a setup report.
1. From the Main Menu, press System Configuration > More > Print
Setup Report.
2. On the Print Setup Report window, select which report to print.
 Basic Setup  Country Setup

 Resting Setup  Patient Setup
 RR Analysis Setup  User Setup
 Arrhythmia Setup  Options Setup
 Communication Setup  Complete Setup
3. When you are done, press the Return softkey to go to the Main Menu.

Select Setup
The Select Setup utility allows you to save up to five system
configurations and switch between them. This is useful if the device is
shared by departments or used in multiple clinical trials.
Use the following instructions to save and load configuration files.
Select Setup.
The Select Setup window opens. The name of the setup currently
being used by the system appears in the Loaded Setup field.
2. To save a copy of the current setup, do the following:
a. Press the Save As softkey.
The Setup Name window opens.
b. Type a name for the configuration and press the Save softkey.
The configuration is saved, and the Setup Name window closes.
3. To load a different setup, do the following:
a. Select the setup to load.
b. Press the Load Setup softkey.
c. Reboot the unit.
The unit must be powered off and on for all setup changes to take
effect, especially if the new setup includes a change to the
language setting: language will not change until the unit reboots.
4. To delete a setup file, do the following:
a. Select the file to delete.
b. Press the Delete softkey.
You are prompted to confirm the deletion.
c. Press OK.
NOTE
You cannot delete a configuration that is currently loaded.
5. To change the name of a system setup file, do the following:
a. Select the setup file to change.
b. Press the Edit Name softkey.
The Setup Name window opens.
c. Type the new name and press the Save softkey.
6. To remove all custom settings, do the following:
a. Select the setup file to reset.

b. Press the Factory Defaults. softkey
c. When prompted to confirm, press Save.
7. When you are done, press the Return softkey to exit.
Export Setup
The Export Setup utility allows you to export saved settings from the
MAC 800 system to an SD card. This SD card can then be used to import
the settings to another MAC 800 system, greatly simplifying the
installation and configuration of multiple MAC 800 systems.
1. Insert the SD card.
Export Setup.
The Select Setup for Export window opens. All saved settings on the
device are listed in the left column. All saved settings on the SD card
are listed in the right column.
3. In the left pane, select the setup file to be exported.
4. Press the Export softkey.
The selected file is copied to the SD card and appears in the right
column.
5. Repeat step 3 through step 4 for each saved configuration file to be

exported.
6. When you are done, press the Return softkey.
Import Setup
The Import Setup utility allows to import up to five system setup files
from another MAC 800 system that were exported to an SD card. This
feature is useful to sites with multiple systems that need to have the
same or similar setups.
1. Insert the SD card with the saved setup file.
Import.
The Select Setup for Import window opens. All saved settings on the
device are listed in the left column. All saved settings on the SD card
are listed in the right column.
3. In the right pane, select the setup file to be imported.
4. Press the Import softkey.
The selected file is copied to the device and appears in the left
column.

5. Repeat step 3 through step 4 for each saved configuration file to be

imported.
6. When you are done, press the Return softkey.
Exporting Audit Trail

The Export Audit function copies the system audit trail in XML format to
an SD card. The Audit Trail tracks the creation, transmission, and
deletion of records; changes to the system setup; and the ID of the users
who made each change.
Audit trail log files are saved to the audittrail directory on the SD card.
Their filenames are in the format audittrail_x.log, where x is a number.
When a log file is saved to the SD card, the system determines whether
the card already contains an audit trail log file and names the new file
accordingly. For example, if the card does not contain a log file, the new
file will be named audittrail_0.log; subsequent files are incremented
by 1: audittrail_1.log, audittrail_2.log, audittrail_3.log, and so on.
After the log file is exported to the SD card, it is cleared from the MAC
800 system.
GE Healthcare recommends exporting the audit trail weekly to long term

storage to meet archive requirements. If the audit trail is not exported
regularly, it will consume storage space and reduce the number of ECGs
that can be stored on the device
To export an audit trail, the following conditions must be met:
 High Security Mode must be enabled.

See “Basic Setup” on page 9-2.
 Audit Trail must be enabled.
See “Basic Setup” on page 9-2.
 The user must have the Edit Setup and Delete Records permissions
set.
See “User Setup” on page 9-21.
Use the following instructions to export the audit trail to an SD card:
1. Insert an SD card into the MAC 800 unit.
More > Export Audit.
When the audit trail has been copied to the SD card and cleared from
the system, a message will appear to notify you the transfer was
successful.
After the XML file has been exported, you can review or print the audit
trail as needed. For more information on how to parse the XML file for
viewing or printing, refer to the GE Cardiology Open XML manual
(PN 2025762-163).

10 Maintenance

Maintenance
Introduction
Regular maintenance, irrespective of usage, is essential to ensure that
the equipment functions when required. This chapter provides basic
maintenance information for the following components:
 MAC 800 device

 Cables and leadwires
 Paper
 Battery
 Supplies and accessories
See the documentation provided with your peripherals for additional

maintenance procedures.
WARNING
MAINTENANCE — Failure on the part of all responsible
individuals, hospitals, or institutions employing this
device to implement the recommended maintenance
schedule may result in equipment failure and possible
health hazards. 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 employing the device.
MAC 800 Maintenance

The MAC 800 ECG Analysis System is designed to require little more
than regular inspection and cleaning to function properly. Any additional
maintenance should be performed by qualified GE service personnel.
CAUTION
ELECTRICAL HAZARD — Improper handling during
inspection or cleaning could result in electrical shock. To
avoid potential shock, observe the following guidelines at
all times:
 Before inspecting or cleaning the system, turn it off,

unplug it from AC power, and remove the battery.
 Do NOT immerse any part of the equipment in water.

Maintenance
Inspecting the Equipment

Perform a visual inspection daily, preferably before the equipment’s first
use each day. During the inspection, verify that the device meets the
following minimum conditions:
 The case and display screen are free of cracks and other damage.
 All plugs, cords, cables, and connectors are free of kinks, frays, and
other damage.
 All cords and connectors are securely seated.
 All keys and controls operate properly.
If you notice any items that need repair, contact an authorized service
representative to make the repairs. Discontinue using the device until
the appropriate repairs can be made.
Cleaning the Device

Clean the exterior surface of the MAC 800 device monthly, or more
frequently if needed.
Cleaning Materials to Use

Use the following materials to clean the device:
 Mild dishwashing detergent

 Clean, soft cloth (2)
 Water
Cleaning Materials to Avoid

DO NOT use any of the following materials to clean the device, because
their use may damage equipment surfaces.
 Organic solvents
 Ammonia-based solvents
 Abrasive cleaning agents
 Alcohol
 Virex
 Sani-Master
Cleaning the MAC 800 Surfaces

Use the following procedure to clean the surfaces of the MAC 800 device.
1. Dilute mild dishwashing detergent in water to create a cleaning

solution.
2. Soak a clean cloth in the solution and wring out any excess.

Maintenance
3. Thoroughly wipe the surface of the MAC 800 device with the damp
cloth.
Do NOT drip the solution or any liquid on the writer assembly.
Avoid contact with open vents, plugs, or connectors.
4. Repeat step 2 and step 3 as necessary until the surface is adequately

cleaned.
5. Wipe the surfaces with a dry, clean cloth or paper towel.
Cable and Leadwire Maintenance

Proper care and maintenance of the cables and leadwires used by the
MAC 800 ECG Analysis System consists of:
 Cleaning the cables and leadwires,

 Storing the cables and leadwires, and
 Replacing the cables and leadwires.
NOTE
The information in this section applies to the Multi-Link acquisition
cable and leadwires.
Sanitizing Cables and Leadwires

Cables and leadwires come into contact with patients and, therefore,
should be cleaned and disinfected after every use. If necessary, they can
also be sterilized.
Before cleaning and disinfecting the cables and leadwires, you need to
know:
 What cleaning materials can be used

 What disinfectants can be used
 What cleaning materials should be avoided
Cleaning Materials to Use

Use the following materials to clean the cables and leadwires:
 Mild dishwashing detergent

 Clean, soft cloth (2)
 Water
Disinfectant to Use
In accordance with the APIC Guidelines for Selection and Use of
Disinfectants (1996), use sodium hypochlorite (5.2% household bleach) to
disinfect the cables and leadwires.

Maintenance
Sodium hypochlorite can be in the form of a liquid or a wipe as long as it

falls within the following range:
 Minimum dilution of 1:500 (minimum of 100 ppm free chlorine)

 Maximum dilution of 1:10
Cleaning Materials To Avoid

DO NOT use the following materials to clean the cables or leadwires:
 Sani-Cloth® Wipes
 Ascepti® Wipes
 HB Quat®
 Clorox® Wipes
 Over-the-counter detergents (Fantastic®, Tilex®, etc.).
 Conductive solutions
 Solutions or products that contain any of the following:
 Abrasive cleaners or solvents
 Acetone
 Alcohol-based cleaning agents
 Ammonium Chloride
 Betadine
 Chlorides, wax, or wax compounds
 Ketone
 Sodium salts
Use of these materials or materials that contain similar active
ingredients and solutions could result in:
 Product discoloration,
 Metal part corrosion,
 Brittle wires and connectors,
 Reduced product life,
 Unit malfunction, and
 Void warranty.
Cautions
Observe the following cautions when cleaning cables and leadwires:
 Never immerse cables or leadwires in any liquid.

 Never pour or spray any liquid directly onto cables or leadwires
 Never permit fluid to seep into connections or openings.
 Never autoclave or steam clean cables or leadwires.
 Always wipe gently to avoid pulling long wires from the connectors.
 Always remove cables and leadwires from the device before cleaning.
Failure to observe these cautions could result in damage to the contact
metal ends, thereby affecting signal quality.

Maintenance
Cleaning Cables and Leadwires

Use the following procedure to clean the cables and leadwires.
NOTE
Cleaning removes dirt and marks but does not disinfect.
1. Dilute mild dishwashing detergent in water to create a cleaning

solution.
2. Soak a clean cloth in the solution and wring out any excess.
3. Thoroughly wipe the exterior of the cables and leadwires with the
damp cloth.
4. Repeat step 2 and step 3 as necessary until adequately cleaned.
5. Wipe with a dry, clean cloth or paper towel and let air dry.
Disinfecting Cables and Leadwires

Use the following procedure to disinfect the cables and leadwires.
NOTE
Clean and dry the cables and leadwires before disinfecting them.
1. Use a lint-free cloth or wipe with a solution of Sodium Hypochloride.
2. Wring excess liquid from the cloth.
3. Gently wipe the cabling.
4. Wipe off the disinfectant with a clean, lightly moistened cloth.
NOTE
If fluid pools around the connectors, blot dry with a soft, lint-free
cloth.
5. Wipe with a dry, lint-free cloth and let air dry for at least 30 minutes.
NOTE
Drying times vary based on the environmental conditions.
DO NOT use excessive drying techniques, such as ovens, forced

heat, or sun drying.
Sterilizing Cables and Leadwires

Although NOT RECOMMENDED, cables and leadwires can be sterilized
with ethylene oxide gas (EtO) at a maximum temperature of 50° C
(122° F). Follow the instructions provided by the sterilizer manufacturer.
NOTE
Frequent sterilization reduces the useful life of cables and leadwires.

Maintenance
Storing Cables and Leadwires

To ensure that the cables and leadwires are in proper working order, use
the following guidelines to store them between use:
 Store in a dry, well-ventilated area.

 Hang cables and leadwires vertically.
 Do not coil cables or leadwires around the device.
Replacing Leadwire Adapters

Although proper cleaning and storage prolong the life of leadwires, you
will eventually need to replace the leadwire adapters. The following
illustration shows the proper method for replacing adapters.
23A

Maintenance
Paper Maintenance
For the proper handling of the MAC 800 thermal writer, you need to
know how to:
 Replace paper
 Store thermal paper
Replacing Paper
Use the following procedure to replace the paper in the MAC 800 thermal
writer.
058A
1. Press the paper tray release button and lift the writer door.
2. Open the writer door fully.
3. Make sure the paper lift tab is pulled forward.
4. Place the pad of paper into the paper compartment on top of the
paper lift tab.
5. Fold out the first sheet of the pad to the right and close the door,
taking care to position the paper on the positioning mark on the top
cover.
6. Press the writer door firmly until it latches.

Maintenance
Storing Thermal Paper

To avoid deterioration or fading of thermal paper and ensure maximum
image life, follow these precautions:
 Store thermal paper separately in manila folders or polyester/

polyimide protectors.
 Keep the paper cool and dry.
Temperature must be below 86°F (30°C). Relative humidity must be
<65%.
 Avoid exposure to bright light or ultraviolet sources.
Sunlight, fluorescent lights, and similar lighting cause yellowing of
paper and fading of tracings.
 Avoid contact with cleaning fluids and solvents, such as alcohols,
ketones, esters, ether, and so on.
 Do not use mounting forms, pressure-sensitive tapes, and labels that
use solvent-based adhesives.
Use only products with starch- or water-based adhesives.
 Keep the paper separate from the following:
 carbon and carbonless forms
 non-thermal chart papers
 any products containing tributyl phosphate, dibutyl phthalate, or
any other organic solvents (often contained in medical and
industrial charts)
 document protectors, envelopes, or sheet separators made of
polystyrene, polypropylene, polyethylene, polyvinyl chloride, or
other vinyl chlorides
Battery Maintenance
The MAC 800 ECG Analysis System uses a rechargeable battery
containing lithium-ion cells. The battery contains an integrated
electronic fuel gauge and a safety protection circuit.
Because of the bias current needed to operate the integrated electronics,

the battery will discharge even when it is not installed in the device. The
rate at which it discharges is dependent on the ambient temperature at
which it is stored. The higher the temperature, the more quickly it
discharges. To prolong the battery’s charge when not in use, store the
battery in a cool, dry location.
A new, fully-charged battery should last for approximately 2 hours of

normal operation. An on-screen gauge indicates the condition and
capacity of the battery’s charge. (For more information on the battery
gauge, refer to “Front View” on page 2-2 and “System Errors” on
page A-6). When the gauge flashes amber, connect the MAC 800 system
to AC power to charge the battery to full capacity.

Maintenance
As the battery ages, the full charge capacity of the battery will degrade
and be permanently lost. As a result, the amount of charge that is stored
and available for use is reduced. When the capacity is no longer sufficient
for your daily operation, you will need to replace the battery.
Battery Safety
Observe the following warnings whenever handling the MAC 800
battery.
WARNING
EXPLOSION OR FIRE — Using non-recommended
batteries could result in injury/burns to patients or users
and may void the warranty.
Use only batteries recommended or manufactured by GE.
WARNING
PHYSICAL INJURY — Leaks from battery cells can
occur under extreme conditions. The liquid is caustic to
eyes and skin.
If the liquid comes in contact with eyes, skin, or clothing,

flush with clean water and seek medical attention.
WARNING
BATTERY PACK DISPOSAL — Do NOT dispose of the
battery by fire or burning.
Follow local environmental guidelines concerning disposal

and recycling.
Replacing the Battery

When the battery’s full-charge capacity can no longer operate the MAC
800 device for an adequate length of time, use the following instructions
to replace the battery.

Maintenance
059A
Conditioning the MAC 800 Battery Pack

To maintain the storage capacity of the battery installed in the MAC 800
unit, GE recommends that you condition the battery once every 6 months
to recalibrate its electronic fuel gauge. A condition cycle consists of an
uninterrupted “charge-discharge-charge” cycle.
Use the following instructions to condition the MAC 800 battery.
1. Insert the battery into a MAC 800 unit that is not being used to
record patient tests.
For details, refer to “Replacing the Battery” on page 10-10.
2. Disconnect the AC mains power from the MAC 800 unit.
3. Enter the Battery Status Service Diagnostic window.
For details on how to access the Battery Status Service Diagnostic

window, refer to the MAC 800 Resting ECG Analysis System Service
Manual.
4. Allow the battery to discharge until its Charge Level is less than
90%.
5. Turn off the unit and reconnect the AC mains power.
6. Allow the battery to fully charge.
The Battery LED will be solid amber while it is charging and turn
off when charging is complete.

Maintenance
7. Remove the AC mains power and turn on the MAC 800 unit.
8. Allow the battery to discharge until MAC 800 unit shuts down.
9. Reconnect the AC mains power to the MAC 800 unit and leave the
unit turned off.
10. Allow the battery to fully charge.
When the Battery LED indicator stops flashing and turns solid, the
battery is fully charged and the conditioning cycle is complete.
Supplies and accessories

For a list of available supplies and accessories for the MAC 800 ECG
Analysis System, refer to the MAC 800 ECG Analysis System Service
Manual (2031504-159).

A Troubleshooting
2031504-182F MAC™ 800 Resting ECG Analysis System A-1

Troubleshooting
General Troubleshooting Tips

The following general troubleshooting tips can be used to help diagnose
problems not specifically discussed elsewhere in this chapter.
 Thoroughly inspect the equipment.

Disconnected or loose cables, missing hardware, and damaged
equipment can cause what may appear to be unrelated symptoms or
equipment failure.
For additional information, refer to “Inspecting the Equipment” on
page 10-3.
 Verify the equipment has not been modified.
Unauthorized modifications to the equipment may cause unexpected
results, poor performance, or system failure.
If the equipment has had unauthorized modifications, contact GE
Technical Support.
 Verify the software has not been updated.
Updated software may change system functionality. If the user is
unaware of the changes, they may appear as unexpected results.
If the software has been updated, refer to the revised Operator’s
Manual to determine whether the update changed features.
 Verify whether there have been changes in the equipment’s location
or environment that could cause the failure.
For example, equipment that emits radio waves could cause
interference during acquisition.
If the environment or location has changed, try using the equipment
in the original location to determine whether the problem persists.
 Verify the problem was not caused by operator error.
Repeat the scenario and compare that to the operation as described
in the manual. If the operator deviated from the manual, repeat the
task using the instructions as written.
If these steps do not resolve the problem, refer to the following section for
specific problems and solutions. If the problem still cannot be resolved,
contact GE Technical Support.
Equipment Problems
The following issues are discussed in the remainder of this chapter.
 “System Will Not Power Up” on page A-3

 “ECG Data Contains Noise” on page A-3
 “ACI-TIPI Statement is Not Included on Report” on page A-4
 “Cannot Export to Shared Directories” on page A-5
A-2 MAC™ 800 Resting ECG Analysis System 2031504-182F

Troubleshooting
System Will Not Power Up

If the system will not power up, do the following:
 Verify the unit is turned on.

If it is not, turn the unit on. Refer to “Turning on the System” on
page 2-12 for instructions.
 Verify the battery is installed and charged.
Refer to “System Errors” on page A-6 for instructions on verifying
whether the battery is installed and charged.
Refer to “Replacing the Battery” on page 10-10 for instructions on
installing the battery.
 Verify the unit is connected to an AC power outlet.
Refer to “Connecting the AC Power Adapter” on page 2-9 for
instructions.
 Verify the equipment is receiving power from the outlet.
If the unit is receiving power, the Power LED will be lit.
ECG Data Contains Noise

If the acquired ECG data displays unacceptable noise levels, do the
following:
 Check the patient’s position.

The patient should remain motionless during the acquisition of a
resting ECG.
 Use Hookup Advisor to help determine the cause of the noise.
For more information, refer to “Hookup Advisor” on page 5-12
 Verify the electrodes are placed properly.
Refer to “Applying Electrodes” on page 3-3 for information on proper
electrode placement.
 Verify the electrodes have been applied correctly.
Perspiration, excessive hair, lotions, and dead skin cells must be
removed from the electrode site.
Refer to “Prepare the Patient’s Skin” on page 3-2 more information.
 Check for defective or expired electrodes.
Replace the electrodes if there are any questions about their
effectiveness.
 Check for defective, broken, or disconnected leadwires.
Replace the leadwires if there are any questions about their
effectiveness. Refer to “Connecting Leadwires” on page 2-10.
 Consider using filters and ADS to help eliminate or reduce ECG
noise.
For more information, refer to “ECG Options” on page 5-4 or
“Arrhythmia Options” on page 6-3.

Troubleshooting
ACI-TIPI Statement is Not Included on Report

If the ACI-TIPI statement does not appear when expected, do the
following:
 Verify the ACI-TIPI option is activated.

For information on activating the ACI-TIPI option, refer to “Options
 Verify ACI-TIPI is enabled on the ECG.
For information, refer to “Resting ECG Setup” on page 9-5.
 Verify the ACI-TIPI required information was entered.
The ACI-TIPI statement will print only if the patient’s gender, date
of birth, and chest pain indication are included in the patient
information.
 Verify the patient is 16 or older.
The ACI-TIPI statement will not print for pediatric patients.
 Verify the original ECG was acquired in an electrocardiograph with
the ACI-TIPI option.
If you attempt to print an ECG that was imported from an external
device, the MAC 800 device will not generate an ACI-TIPI statement;
it will print only if the statement was saved as part of the ECG.
Paper Jams
If the paper jams while printing, verify the paper was inserted correctly.
For details, refer to “Replacing Paper” on page 10-8.
SD Card Not Present

If you receive an error message stating that the SD card is not present or
cannot be found, do the following:
 Verify an SD card is inserted into the card slot on the back of unit.
For details, refer to “Back View” on page 2-3.
 Verify the SD card is seated firmly.
The SD card will click into place when seated firmly.
 Verify the SD card is formatted for FAT or FAT16 file systems.
To verify an SD card is formatted for FAT or FAT16 file systems, do
the following:
1. Insert the card into an SD card reader attached to a PC.
2. Copy any files to keep from the SD card to a folder on the PC.
3. Using the Windows Format command, specify either FAT or
FAT16 as the file system and format the card.
NOTE
Formatting the SD card will erase any existing files on the
card.

Troubleshooting
4. Copy the files from the folder on the PC to the newly formatted
SD card.
Cannot Import or Transmit Records Via Modem

If you receive an error while attempting to import or transmit ECG
records via modem, do the following:
 Verify the correct communication option has been activated.

The MAC 800 system supports two options for communicating via
modem: MODC (for communicating with a Cardiosoft system) and
MODM (for communicating with a MUSE system). For more
information, refer to “Options Setup” on page 9-23.
 Verify the modem is connected to an analog telephone line using a
standard RJ11 phone jack.
For more information, refer to “Back View” on page 2-3.
 Check Communications Setup to:
 Verify the correct modem type is selected.
 Verify the correct dialing method is selected and configured
accurately.
For details, refer to “Communication Setup” on page 9-13.
 If transmitting records, check the selected location to:
 Verify Modem is the selected device.
 Verify the Phone Number is correct.
 Verify the correct Protocol is selected.
For details, refer to “Communication Setup” on page 9-13.
Cannot Export to Shared Directories

To resolve errors received while attempting to export ECG records to a
shared directory, do the following:
 Verify the LANC communication option has been activated.

Refer to “Options Setup” on page 9-23 for information on activating
options.
 Verify connectivity by doing the following:
 Verify that the network cables are connected.
 Verify the IP, netmask, gateway, and DNS server addresses are
all correct.
Refer to “Communication Setup” on page 9-13 for instructions on
setting these values.
 Ping the MAC 800 unit from the file server to verify that the two
devices can communicate.
 Verify the logon information is correct.
Check the user name, password, and domain information. Refer to
“Communication Setup” on page 9-13 for information on the logon
information.

Troubleshooting
 Verify share and directory permissions.

Ensure that the account used to log on to the shared directory has
read/write/create permissions to both the share and the directory.
Refer to Windows online help for instructions on how to set user
permissions.
System Errors
The following table identifies some potential errors that may occur while
you are operating the system, the possible causes, and a recommended
course of action to resolve the error.
If performing the recommended actions does not resolve the problem,

contact authorized service personnel.
Problem Cause Solution
Battery Error message displays The battery is installed incorrectly, or the Verify the battery contacts are clean.
batter is not functioning correctly.
Notify service to check and replace the
battery.
The battery LED flashes intermittently Battery charge is low. Connect the system to an AC wall outlet to
when operating from battery power. charge the battery.
The writer door is open message displays The writer door is closed incorrectly. Close the door correctly.
The system powers down while operating Battery is fully discharged Connect the system to an AC wall outlet to
from battery power. charge the battery or power the unit.
Lead disconnected message displays One or more electrodes is disconnected. Reconnect the electrodes.
MODEM ERROR: The remote device is Modem is not connected. Connect the modem and retry, or move
not responding. Would you like to retry? back into range.
(Ethernet option only) Bad LAN connection Verify that the LAN cable is connected to
the LAN port, the link LED (Green) lights,
and the Activity LED (Yellow) flashes.

B Creating Barcodes
2031504-182F MAC™ 800 Resting ECG Analysis System B-1

Creating Barcodes
Introduction
The barcode reader can read any of the following symbologies:
 Code 39
 Code 39EX
 Code 128
 PDF-417
 Interleaved Code 2 of 5
 Data Matrix
Regardless of which symbology is used, the site’s IT department must:
 set up the patient data scheme

 configure the barcode reader
Setting up the Patient Data Scheme

Use the following rules to set up a data scheme, including patient
demographic data, for your barcodes.
Item Byte Length
Patient ID The Patient ID length should not exceed the 30-character

maximum and should be equal to the ID length set up on the
system in the Patient Setup window.
If the MAC 800 system is communicating with a MUSE

system, the length of the patient ID should also be the same
as that used by the MUSE system.
Last Name 40 (maximum)
First Name 20 (maximum)
Year of birth 4
Month of birth 2
Day of birth 2
Gender 1
B-2 MAC™ 800 Resting ECG Analysis System 2031504-182F

Creating Barcodes
Configuring the Barcode Reader

The barcode reader is configured on the MAC 800 Patient Setup window.
You can choose to configure it manually or automatically. The
requirements for each method are described in the following sections. For
instructions on configuring the barcode reader, refer to “Patient Setup”
on page 9-18.
Configuring the Barcode Reader Manually

To configure the barcode reader manually, you will need to enter the
following information on the MAC 800 Patient Setup window.
Field Number of bytes
Total number of bytes ________
Patient ID offset ________
Patient ID length ________
First name offset ________
First name length ________
Last name offset ________
Last name length ________
Year of birth offset ________
Year of birth length ________
Month of birth offset ________
Month of birth length ________
Day of birth offset ________
Day of birth length ________
Gender offset ________
Gender length ________
2031504-182F MAC™ 800 Resting ECG Analysis System B-3

Creating Barcodes
Configuring the Barcode Reader Automatically

The barcode reader can be configured automatically by scanning a bar
code that has been set up to identify the fields on the barcode, their
offset, and their maximum length.
A field is identified by using its corresponding code. The field codes are
shown in the following table.
Field Code
Month of birth 1
Day of birth 2
Year of birth 3
First name 5
Last name 6
Patient ID 9
Gender F
A field’s offset, or position, is determined by the order in which its field

code appears.
The field length is determined by the number of times its field code is
repeated.
For example, suppose you want the following information in the barcode.
Field Length
Patient ID 10
Last Name 15
First Name 10
Gender 1
This information would be set up as follows:
99999999996666666666666665555555555F
Because the barcode is set up for fixed length fields, the barcode
generator must be programmed to add trailing spaces if data is shorter
than the maximum field length. For example, using the previous
configuration, a patient barcode may appear as follows:
1234567890Jones Robert M
B-4 MAC™ 800 Resting ECG Analysis System 2031504-182F

C Magnetic Card Reader
Configuration
2031504-182F MAC™ 800 Resting ECG Analysis System C-1

Magnetic Card Reader Configuration
Introduction
A magnetic card contains patient data in the form of a string of
fixed-length fields, as seen in the following example.
The following table describes each field in the record.
Position
Name Comment Length Starting Ending
A Data Header Separates records 1 1 1
B Patient ID Unique ID 6 2 7
C First Name Given name 13 8 20
D :Last Name Surname 10 21 30
E Birth Date 01-31 2 31 32
F Birth Month 01-12 2 33 34
G Birth Year Examples: 1960, 1985, 2008 4 35 38
H Gender F, M 1 39 39
Total bytes: 39
NOTE
The field lengths, order, and positions shown are examples only.
They will most likely differ on your system.
Understanding the Data Header

Before configuring the MAC 800 system’s magnetic card reader, you need
to understand the impact of the data header on the configuration file.
The data header is a special character that indicates the beginning of a

record. ISO standards dictate that the header should be a semicolon ( ; ).
The way in which the magnetic card reader handles the data header
affects the configuration file. Some card readers include the data header
when it reads the records. Others strip it out. You need to account for
this difference when you define Offset and Total Bytes in the magnetic
card reader’s configuration file.
C-2 MAC™ 800 Resting ECG Analysis System 2031504-182F

Use the following procedure to identify how the magnetic card reader
handles the data header.
1. Connect a magnetic card reader to a PC.
2. Run Microsoft Notepad or some other ASCII text editor.
3. With Notepad active, swipe a magnetic card through the card reader.
The information on the card will appear in Notepad.
4. Examine the record in Notepad.
 If the first character is a semi-colon, the card reader includes the

data header.
The Offset of each field and the Total Bytes of the configuration
file need to be increased by 1.
 If the first character is alphanumeric, the card reader strips the
data header.
Configuring the Magnetic Card Reader

You configure the magnetic card reader on the MAC 800 Patient Setup
window (see “Patient Setup” on page 9-18). To configure the card reader
for the example in the introduction, you would enter the information
shown in the following table.
Field Offset Length
Patient ID 1 6
First name 7 13
Last name 20 10
Year of birth 34 4
Month of birth 32 2
Day of birth 30 2
Gender 38 1
39
Offset is the number of characters to the left of the field, not the field’s
starting position. To calculate the Offset, add the Offset and Length of
the preceding field in the record. For example, the Offset of First Name is
7, which is the Patient ID Offset (1) plus the Patient ID Length (6).
NOTE
Patient ID has an Offset of 1 because it is preceded by the single
character data header. If the magnetic card reader stripped the
header from the record, the Patient ID Offset would be 0, and all
subsequent Offsets would shift accordingly.
2031504-182F MAC™ 800 Resting ECG Analysis System C-3

Total Bytes is the sum of all the field lengths in the record. If the card
reader includes the data header, Total Bytes is the sum of all field
lengths plus the data header. In this case, the sum of all field lengths is
38; add a length of one for the data header and the Total Bytes is 39.
C-4 MAC™ 800 Resting ECG Analysis System 2031504-182F

Index
Index
Numerics B
12 Lead Display for Resting ECG ......................... 9-24 barcode reader
12SL Measurement............................................... 9-24 configuring ...................................................... 9-21
12SL Measurement and Interpretation ................. 9-24 connecting to .................................................. 2-11
21 CFR Part 11 Audit Trail .................................... 9-24 entering patient information ....................... 4-3, 4-4
option.............................................................. 9-24
A
settings ........................................................... 9-21
A (artifact) ............................................................... 6-5
baseline shift, reducing ........................................... 6-4
AC power, connecting to ......................................... 2-9
Basic Setup
accessories
audit trail ........................................................... 9-4
and parts......................................................... 1-12
auto logoff......................................................... 9-4
recommended................................................. 1-12
auto standby ..................................................... 9-4
ACI-TIPI
high security mode ........................................... 9-4
including ......................................................... 9-10
overview ........................................................... 9-2
option.............................................................. 9-24
power up mode................................................. 9-3
acquisition cable
time synchronization......................................... 9-4
connector.......................................................... 2-3
battery
types ................................................................. 2-6
charging............................................................ 2-9
Acute Cardiac Ischemia-Time Insensitive Predictive
inserting ........................................................ 10-10
Instrument, see ACI-TIPI
LED................................................................... 2-2
ADS
lithium-ion ......................................................... 2-9
definition ........................................................... 6-4
maintenance ................................................... 10-9
on arrhythmia setup........................................ 9-12
replacing ....................................................... 10-10
turn off during defibrillation ............................. 1-11
safety ............................................................ 10-10
Allow Export Using Shared Directory .................... 9-14
BCRD option ................................................ 2-11, 9-24
Anti-Drift System, see ADS
biocompatibility statement..................................... 1-10
arrhythmia codes .................................................... 6-5
Blood Pressure Unit .............................................. 9-17
Arrhythmia ECG
display .............................................................. 6-2 C
mode................................................................. 6-2 Cardiogoraph Device Name.................................. 9-16
options .............................................................. 6-3 Cardiosoft system
printing an arrhythmia report ............................ 6-2 communication option..................................... 9-24
printing options ................................................. 6-5 CDTG option ......................................................... 9-24
Arrhythmia Event Printing ..................................... 9-13 CFRA option .................................................. 9-4, 9-24
Arrhythmia Setup CISPR 11 ................................................................ 1-9
ADS ................................................................ 9-12 cleaning
episode printout .............................................. 9-13 disinfectant to use........................................... 10-4
event printing .................................................. 9-13 disinfecting leadwires ..................................... 10-6
lead sequence ................................................ 9-13 leadwires ........................................................ 10-6
overview ......................................................... 9-12 materials to avoid .................................. 10-3, 10-5
artifact ..................................................................... 6-5 materials to use ..................................... 10-3, 10-4
ASYSTO (asystole) ................................................. 6-5 sterilizing leadwires ........................................ 10-6
asystole ................................................................... 6-5 communication protocol ........................................ 9-15
Audit Trail ................................................................ 9-4 Communication Setup
auto configuring a barcode reader ........................ 9-21 cardiogoraph device name ............................. 9-16
Auto Logoff.............................................................. 9-4 default location ............................................... 9-13
Auto Standby .......................................................... 9-4 device ............................................................. 9-15
Auto Store ECG .................................................... 9-11 DHCP settings ................................................ 9-16
Auto Transmit ECG ............................................... 9-11 DNS settings................................................... 9-16
location ........................................................... 9-14
overview ......................................................... 9-13
2031504-182F MAC™ 800 Resting ECG Analysis System Index-1

Index
protocol........................................................... 9-15 generating......................................................... 5-9

serial baud rate............................................... 9-14 options ............................................................ 5-11
shared directory settings ................................ 9-14 setup................................................................. 9-9
configurations, switching between ........................ 9-26 editing patient information ....................................... 8-5
connecting EFUP (Environment-friendly Use Period) ............. 1-14
to a barcode reader ........................................ 2-11 EGC Acquisition...................................................... 9-8
to AC power...................................................... 2-9 electrodes
to leadwires .................................................... 2-10 12 Lead placement ........................................... 3-4
conventions ............................................................. 1-3 NEHB placement .............................................. 3-5
Country Setup to use during defibrillation............................... 1-11
blood pressure unit ......................................... 9-17 Enabling Patient ID Check .................................... 9-19
date format ..................................................... 9-17 Episode Printout.................................................... 9-13
height/weight unit............................................ 9-17 equipment
language......................................................... 9-17 safety information ............................................. 1-3
overview ......................................................... 9-17 service requirements ...................................... 1-15
time format...................................................... 9-17 type CF ........................................................... 1-13
CPLT (ventricular couplet) ...................................... 6-5 equipotentional grounding lug ................................. 2-4
CT Data Guard...................................................... 9-24 ESC (ventricular escape beat) ................................ 6-5
CTDG option ........................................................... 4-2 ethylene oxide gas ................................................ 10-6
EtO........................................................................ 10-6
D
Export Setup ......................................................... 9-27
date format ............................................................ 9-17
export XML............................................................ 9-14
Date Setup ............................................................ 9-24
exporting ECG records ........................................... 8-8
daylight savings time............................................. 9-25
Extra Questions .................................................... 9-21
Default Location .................................................... 9-13
defibrillation F
electrodes to use during ................................. 1-11 fiducial points ........................................................ 5-11
recording an ECG during....................... 1-11, 5-14 File Manager
turn off ADS during ......................................... 1-11 deleting records ................................................ 8-6
deleting records ...................................................... 8-6 editing patient information ................................ 8-5
DHCP settings ...................................................... 9-16 exporting records.............................................. 8-8
disinfectant to use ................................................. 10-4 finding records .................................................. 8-4
Display Format ........................................................ 9-7 importing records.............................................. 8-3
Display Lead Group ................................................ 9-7 overview ........................................................... 8-2
DNS settings ......................................................... 9-16 printing directory ............................................... 8-4
Dose List ............................................................... 9-21 printing records................................................. 8-7
Dose Type............................................................. 9-20 transmitting records .......................................... 8-7
filter .................................................................. 5-6, 6-4
E
finding ECG records................................................ 8-4
ECG
frequency response .............................................. 1-12
deleting ............................................................. 8-6
function keys ........................................................... 2-5
editing patient information ................................ 8-5
exporting........................................................... 8-8 G
finding ............................................................... 8-4 gain ............................................ 5-5, 6-4, 7-4, 7-6, 9-6
importing........................................................... 8-3 grounding ................................................................ 2-4
printing.............................................................. 8-7
H
recording during defibrillation ................ 1-11, 5-14
handle
transmitting ....................................................... 8-7
location ............................................................. 2-4
see also
proper use ........................................................ 2-8
Arrhythmia ECG
Height/Weight Unit ................................................ 9-17
Resting ECG
High Pass Filter................................................ 7-7, 9-7
see also RR Analysis mode
High Security Mode................................................. 9-4
ECG reanalysis
Hookup Advisor
conducting ........................................................ 5-9
affected by skin preparation ............................. 3-2
display ............................................................ 5-10
overview ......................................................... 5-12
Index-2 MAC™ 800 Resting ECG Analysis System 2031504-182F

Index
setting up .......................................................... 9-8 replacing leadwire adapters............................ 10-7

sterilizing leadwires ........................................ 10-6
I
storing leadwires............................................. 10-7
Import Setup ......................................................... 9-27
ME12 option.......................................................... 9-24
importing ECG records ........................................... 8-3
menu options
input signal accuracy ............................................ 1-12
selecting ......................................................... 2-13
inspecting a MAC 800 device ............................... 10-3
MI12 option ........................................................... 9-24
internal storage, see File Manager
MODC option ................................................. 9-24, A-5
K modem
Kanji name ............................................................ 9-18 troubleshooting ................................................. A-5
keyboard Modem or serial communication to Cardiosoft...... 9-24
layout ................................................................ 2-5 Modem or serial communication to MUSE............ 9-24
using ............................................................... 2-13 MODM option................................................. 9-24, A-5
KISS Multi-Link acquisition cable ..................................... 2-7
cleaning instructions ....................................... 10-4 MUSE system
communication option..................................... 9-24
L
importing from................................................... 8-3
L (learn phase) ........................................................ 6-5
User ID ........................................................... 9-22
LAN Communication to Cardiosoft........................ 9-24
LAN Communication to MUSE.............................. 9-24 N
LANC option................................................... 8-9, 9-24 navigating with the trimpad ................................... 2-14
LANM option ......................................................... 9-24
O
laser printer ............................................................. 7-5
option
Lead Sequence ............................................ 9-10, 9-13
BCRD .................................................... 2-11, 9-24
leadwire
CDTG ............................................................. 9-24
adapters............................................................ 2-7
CFRA....................................................... 9-4, 9-24
cleaning .......................................................... 10-6
CTDG ............................................................... 4-2
connecting to .................................................. 2-10
LANC ....................................................... 8-9, 9-24
replacing adapters .......................................... 10-7
LANM.............................................................. 9-24
sanitizing......................................................... 10-6
M100........................................................ 8-2, 9-24
storing............................................................. 10-7
M300............................................................... 9-24
learn phase ............................................................. 6-5
ME12 .............................................................. 9-24
Line Filter ................................................................ 7-5
MI12................................................................ 9-24
lithium-ion battery, see battery
MODC...................................................... 9-24, A-5
Location ................................................................ 9-14
MODM ..................................................... 9-24, A-5
Low Pass Filter ......................................... 7-4, 7-6, 9-6
PDFC.............................................................. 9-24
M R12L ............................................................... 9-24
M100 option ................................................... 8-2, 9-24 RRAN ............................................................. 9-24
M300 option .......................................................... 9-24 setup............................................................... 9-23
magnetic card reader TIPI ................................................................. 9-24
configuring .............................................. 9-21, C-3
P
connecting ...................................................... 2-11
Pace Enhancement................................................. 7-5
data header ...................................................... C-2
pacemaker
data layout ........................................................ C-2
capture code..................................................... 6-6
settings ........................................................... 9-21
improving ECG readability... 5-6, 6-4, 7-4, 7-5, 9-8
maintenance
malfunction ....................................................... 6-6
cleaning leadwires .......................................... 10-6
recording ECGs of patients with ..................... 5-13
cleaning MAC 800 surfaces............................ 10-3
paper
cleaning materials to avoid .................... 10-3, 10-5
problems with ................................................... A-4
cleaning materials to use....................... 10-3, 10-4
replacing ......................................................... 10-8
disinfectant to use........................................... 10-4
storing............................................................. 10-9
disinfecting leadwires ..................................... 10-6
troubleshooting problems with.......................... A-4
inspecting a MAC 800 device ......................... 10-3
parts and accessories ........................................... 1-12
overview ......................................................... 10-2
patient

Index
editing information with File Manager............... 8-5 mode................................................................. 5-2

setup options .............................................................. 5-4
auto configure .......................................... 9-21 post-acquisition options .................................... 5-6
barcode reader settings ........................... 9-21 printing.............................................................. 8-7
custom fields ................................... 9-20, 9-21 reanalyzing ....................................................... 5-9
dose list .................................................... 9-21 recording........................................................... 5-3
dose type.................................................. 9-20 Rhythm Report ................................................. 5-8
enabling ID check..................................... 9-19 saving automatically ................................ 8-2, 9-11
extra questions................................ 9-20, 9-21 saving manually................................................ 8-2
ID type...................................................... 9-19 setup
Kanji name ............................................... 9-18 ACI-TIPI ................................................... 9-10
magnetic card reader settings.................. 9-21 auto store ................................................. 9-11
overview ................................................... 9-18 auto transmit ............................................ 9-11
skin preparation ................................................ 3-2 display format............................................. 9-7
Patient ID Type ..................................................... 9-19 display lead group ...................................... 9-7
patient information gain ............................................................ 9-6
entering manually ............................................. 4-2 high pass filter ............................................ 9-7
entering with a barcode reader.................. 4-3, 4-4 Hookup Advisor.......................................... 9-8
PAU1 (pause of 1 missed beat) .............................. 6-5 lead sequence.......................................... 9-10
PAU2 (Pause of 2 missed beats) ............................ 6-5 low pass filter ............................................. 9-6
pause overview ..................................................... 9-5
1 missed beat ................................................... 6-5 pace enhancement .................................... 9-8
2 missed beats ................................................. 6-5 printer leads ............................................... 9-8
PCAP (pacemaker capture) .................................... 6-6 QTC Calculation......................................... 9-9
PDF export .............................................................. 7-5 reanalysis ................................................... 9-9
PDFC sweep speed .............................................. 9-6
option.............................................................. 9-24 transmitting .............................................. 8-7, 9-11
PDFC option ......................................................... 9-24 Rhythm Record ....................................................... 7-7
PERR (pacemaker malfunction) ............................. 6-6 Rhythm Report ........................................................ 5-8
PIN dialing............................................................. 9-15 RR Analysis
Power Up Mode ...................................................... 9-3 post-test options ............................................... 7-5
printer leads ..................................................... 5-6, 9-8 pre-test options................................................. 7-3
printing ECG records .............................................. 8-7 printing an RR Analysis Report ........................ 7-2
product code ......................................................... 1-16 setup
protocol gain ............................................................ 7-6
communication ............................................... 9-15 high pass filter ............................................ 7-7
PSVC (premature supraventricular contraction) ..... 6-6 line filter...................................................... 7-5
PVC (premature ventricular contraction)................. 6-6 low pass filter ............................................. 7-6
pace enhancement .................................... 7-5
Q
record lead ................................................. 7-5
QRSL (learned QRS complex)................................ 6-6
rhythm record ............................................. 7-7
QTC Calculation...................................................... 9-9
RR table ..................................................... 7-7
R sweep speed .............................................. 7-6
R12L option........................................................... 9-24 target .......................................................... 7-5
reanalyzing an ECG ................................................ 5-9 test options ....................................................... 7-3
Record Lead ........................................................... 7-5 RR Analysis mode .................................................. 7-2
recording a resting ECG ......................................... 5-3 RR Table................................................................. 7-7
Resting ECG RRAN
deleting ............................................................. 8-6 option.............................................................. 9-24
display .............................................................. 5-2 RRAN option ......................................................... 9-24
editing patient information ................................ 8-5 RUN (ventricular run) .............................................. 6-6
exporting........................................................... 8-8
S
finding ............................................................... 8-4
safety
importing........................................................... 8-3
equipment symbols......................................... 1-13

Index
messages ......................................................... 1-3 time format ............................................................ 9-17

SD card .................................. 2-3, 2-12, 8-8, 9-27, A-4 Time Setup............................................................ 9-24
Secure Digital Card, see SD card ........................... 2-3 time synchronization ............................................... 9-4
Serial Baud Rate ................................................... 9-14 TIPI option............................................................. 9-24
service requirements............................................. 1-15 transmitting ECG records........................................ 8-7
Service Setup, see the MAC 800 Service Manual trimpad
Setup Report ......................................................... 9-25 description ........................................................ 2-5
shared directory ............................................. 8-8, 9-14 navigating with................................................ 2-14
SJ/T11363-2006 ................................................... 1-14 troubleshooting
skin preparation ...................................................... 3-2 basic questions................................................. A-3
Storage for 100 ECGs........................................... 9-24 operator error.................................................... A-2
Storage for 300 ECGs........................................... 9-24 visual inspection ....................................... A-2, A-3
supraventricular type CF equipment................................................ 1-13
premature contraction....................................... 6-6 typographical conventions ...................................... 1-3
Sweep Speed.......................................................... 7-6
U
sweep speed ...................................... 5-5, 6-3, 7-3, 9-6
USB (Universal Serial Bus)..................................... 2-4
symbols ................................................................. 1-13
USB connector ...................................................... 2-11
System Setup
User Setup
Date/Time ....................................................... 9-24
MUSE ID......................................................... 9-22
exporting......................................................... 9-27
overview ......................................................... 9-21
importing......................................................... 9-27
printing............................................................ 9-25 V
switching configurations ................................. 9-26 VBIG (ventricular bigeminy) .................................... 6-6
see also ventricular
Arrhythmia ECG bigeminy ........................................................... 6-6
Basic Setup couplet .............................................................. 6-5
Communication Setup escape beat ...................................................... 6-5
Country Setup fibrillation .......................................................... 6-6
option, setup premature contraction....................................... 6-6
patient, setup run .................................................................... 6-6
Resting ECG tachycardia ....................................................... 6-6
the MAC 800 Service Manual VFIB (ventricular fibrillation/flutter) .......................... 6-6
User Setup visual inspection...................................................... A-2
see also RR Analysis, Setup VTAC (ventricular tachycardia) ............................... 6-6
T X
Target...................................................................... 7-5 XML export............................................................ 9-14

Index

Asia Headquarters
GE Medical Systems GE Medical Systems GE Medical Systems
Information Technologies, Inc. Information Technologies GmbH Information Technologies Asia; GE (China) Co., Ltd.
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T-2 MAC™ 800 Resting ECG Analysis System 2031504-182F

Safety Information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-3

General Information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-11

Service Requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-15

Product Identification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-16

Setting Up the Equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8

2031504-182F MAC™ 800 Resting ECG Analysis System i

System Description. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13

3 Preparing the Patient

Applying Electrodes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-3

4 Entering Patient Information

Entering Patient Information with a Barcode Reader . . . . . . . . . . . . . . . . . . . . . . . 4-3

Entering Patient Information with a Magnetic Card Reader . . . . . . . . . . . . . . . . . . 4-4

5 Recording a Resting ECG

Resting ECGs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3

Generating a Rhythm Report (Manual recording) . . . . . . . . . . . . . . . . . . . . . . . . . . 5-8

ECG Reanalysis. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-9

Hookup Advisor . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-12

Special Considerations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-13

ii MAC™ 800 Resting ECG Analysis System 2031504-182F

6 Arrhythmia Mode Recording

Arrhythmia Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2

Arrhythmia Codes . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-5

RR Analysis Mode. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2

RR Analysis Setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-5

8 Managing Internal Storage

Importing Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-3

Printing the File Manager Directory . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4

Finding Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-4

Editing Patient Data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-5

Deleting Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-6

Printing Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-7

Transmitting Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-7

Exporting Records . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8

PDF File Naming Convention . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11

2031504-182F MAC™ 800 Resting ECG Analysis System iii

Setup Functions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2

Setup Utilities . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-25

MAC 800 Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-2

Cable and Leadwire Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-4

Paper Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-8

Battery Maintenance . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-9

Supplies and accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-12

iv MAC™ 800 Resting ECG Analysis System 2031504-182F

System Errors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-6

Setting up the Patient Data Scheme . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-2

Configuring the Barcode Reader. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-3

C Magnetic Card Reader Configuration

Understanding the Data Header . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-2

Configuring the Magnetic Card Reader . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-3

2031504-182F MAC™ 800 Resting ECG Analysis System v

2031504-182F MAC™ 800 Resting ECG Analysis System 1-1

Revision History, PN 2031504-182

Revision Date Comment

A 11 July 2008 Initial release of document.

B 15 August 2008 Revised document assembly instructions.

C 10 October 2008 Various changes per validation results.

D 5 December 2008 Various changes per pilot site feedback.