GE MP100 Series, CIC Pro Service Manual

GE Healthcare
CIC Pro™ Clinical Information Center
Software Version 5.1 MP100 Series
CIC Pro™ English 2026420-003 (CD) 2026421-026E (paper) © 2008-2010 General Electric Company. All rights reserved.
NOTE
The information in this manual only applies to CIC Pro center software versions 5.1.x or later. It does not apply to earlier software versions. Due to continuing product innovation, specifications in this manual are subject to change without notice.
NOTE
For technical documentation purposes, the abbreviation GE is used for the legal entity name, GE Medical Systems Information Technologies, Inc.
NOTE
The product names CIC Pro, CIC Pro center, CARESCAPE CIC Pro Clinical Information Center , CARESCAPE CIC Pro, CARESCAPE CIC Central Station, CARESCAPE Clinical Information Center Pro, and CARESCAPE Clinical Information Center all refer to the CIC Pro Clinical Information Center product.
Listed below are GE Medical Systems Information Technologies, Inc. trademarks used in this document. All other trademarks contained herein are the property of their respective owners.
APEX, Aware, SOLAR, and MUSE are trademarks of GE Medical Systems Information Technologies, Inc., registered in the United States Patent and Trademark Office.
APEXPRO, CARESCAPE, CD TELEMETR Y-LAN, CENTRALSCOPE, CIC PRO, and UNITY NETWORK are trademarks of GE Medical Systems Information Technologies, Inc.
T-2 CIC Pro™ 2026419-033E
21 September 2010

Contents

1 Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-1
Equipment information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
License agreement. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-2
Intended use of the equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4
Safety information. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-4
Equipment symbols . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-9
Service requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-11
Manufacturer responsibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-12
Equipment identification . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-12
Manual information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-13
Manual purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-13
Intended audience . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-13
Related manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-13
Conventions used. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-13
Ordering manuals . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-14
Revision history . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 1-14
2 Equipment overview . . . . . . . . . . . . . . . . . . . . . . . . . 2-1
Standard components. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-2
Display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
Processor box . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-3
Controls . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-6
Power indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Optional components . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-7
Secondary display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-8
Touchscreen displays . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
Mirror display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
Laser printer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-9
PRN 50-M digital writer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-10
Un-interruptible power supply (UPS) . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
Theory of operation. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
Functional description . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-11
Block diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
Physiological data. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-12
File and data management. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-13
Licensing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
Full disclosure. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-14
Networking. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-20
Patient monitoring network . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-21
Web access server network . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-21
2026419-033E CIC Pro™ i
Patient data interface . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-22
Multi-patient viewer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-22
Single patient viewer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-24
Patient data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-24
Real-time patient data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-25
Stored patient data . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-25
Service interfaces . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 2-26
3 Licensing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-1
CIC Pro center configurations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
License requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-2
Available licenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
Description of licenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-4
License packages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-6
Patient Data Server information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
License activation methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 3-7
4 Service interfaces . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-1
Introduction . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
Access methods . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
Direct access method . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
Network access method . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-2
Operating modes. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Administrator mode access . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-3
Service interface access. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-4
Setup CIC with service access. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-5
Command-line interface access (for advanced users). . . . . . . . . . . . . . . . 4-5
Windows utilities access . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
Screen-sharing interface access . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-6
Webmin interface access . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-7
Webmin overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9
Information tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-9
Configuration tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-10
Diagnostics tab . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 4-12
5 Installation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-1
Requirements. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2
Complete product training . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2
ii CIC Pro™ 2026419-033E
Complete site survey . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2
Service PC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2
Pre-installation checklist . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-2
Format a USB memory stick . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Procure necessary licenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-3
Gather required tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Inspect equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Evaluate site. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-4
Installation process. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-8
Precautions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-8
Installation process checklist . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-10
Mount the equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-11
Connect the cables and peripheral devices . . . . . . . . . . . . . . . . . . . . . . . 5-12
Remote view (view only). . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-15
Install optional accessories. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-16
Plug in the power cable to the CIC Pro center . . . . . . . . . . . . . . . . . . . . 5-18
Turn on the power . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 5-19
6 Configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-1
Pre-configuration process . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
Pre-configuration requirements . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
Pre-configuration instructions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-2
Configuration process checklist . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7
Disconnect CARESCAPE Network IX and MC networks . . . . . . . . . . . . . 6-7
Install licenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7
Configure Webmin-related settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-7
Configure desktop-related settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-8
Configure clinical application settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-8
Reconnect the CIC Pro center with the network . . . . . . . . . . . . . . . . . . . . . 6-9
Perform MultiKM (Multimouse) setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-9
Run Log File Compression Configuration Utility . . . . . . . . . . . . . . . . . . . . . 6-9
Disconnect from the CARESCAPE Network IX and MC networks . . . . . . 6-10
Configure Webmin-related settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Activate software licenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-10
Set the network IP address . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-12
Configure clinician review workstation . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-14
Configure network laser printers. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-14
Configure the server for remote connectivity . . . . . . . . . . . . . . . . . . . . . . 6-16
Set up a Citrix client . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-19
Configure browser favorites . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-21
Configure set flags settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-22
Configure the CIC Pro center language . . . . . . . . . . . . . . . . . . . . . . . . . 6-27
Configure desktop-related settings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-28
2026419-033E CIC Pro™ iii
Configure USB laser printers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-28
Set the laser printer default paper size . . . . . . . . . . . . . . . . . . . . . . . . . . 6-30
Configure a secondary display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-30
Calibrate a touchscreen display . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-32
Set the time zone . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-34
Restart CIC Pro center . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-36
Configure clinical application settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-36
Configure the printer settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-36
Configure clinical application, telemetry, and care unit settings. . . . . . . . 6-36
Set the Telemetry Unit Defaults . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-44
Set the Telemetry Alarm Control Defaults . . . . . . . . . . . . . . . . . . . . . . . . 6-45
Full disclosure license management setup. . . . . . . . . . . . . . . . . . . . . . . . 6-47
Set the Display Configuration (non-mirror CIC Pro centers) . . . . . . . . . . 6-49
Set the Current Telemetry Listings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-51
Set up locked beds . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-53
(Chinese only) Set the pressures unit-of-measure . . . . . . . . . . . . . . . . . 6-53
Screen calibration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-55
Browser configuration. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-57
Configure customize groupings. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-61
Set up customize groupings for graphic trends . . . . . . . . . . . . . . . . . . . . 6-61
Set up custom groupings for vital signs . . . . . . . . . . . . . . . . . . . . . . . . . . 6-64
Configure shortcuts to favorite CIC Pro center views . . . . . . . . . . . . . . . 6-65
Configure the print location settings for stored patient data . . . . . . . . . . 6-67
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-67
Configure the print location settings for the patient data categories . . . . 6-67
Set the time-of-day or the date . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-68
Back up and restore the CIC Pro center configuration . . . . . . . . . . . . . . . 6-71
Back up care unit default configuration settings . . . . . . . . . . . . . . . . . . . 6-71
Planning your care unit defaults restore strategy. . . . . . . . . . . . . . . . . . . 6-72
Backing up and restoring local custom default configuration settings . . . 6-75
Reconnect the CIC Pro center with the network . . . . . . . . . . . . . . . . . . . . 6-77
Perform MultiKM (Multimouse) setup . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-77
Pre-configure the CIC Pro centers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-78
Configure the keyboard and mouse group . . . . . . . . . . . . . . . . . . . . . . . 6-80
Change a keyboard and mouse group. . . . . . . . . . . . . . . . . . . . . . . . . . . 6-83
Run Log File Compression Configuration Utility . . . . . . . . . . . . . . . . . . . . 6-88
Equipment/tools required . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 6-88
Create a Log File Compression Configuration Utility USB memory stick 6-88
Run Log Compression Configuration Utility . . . . . . . . . . . . . . . . . . . . . . . 6-89
Complete configuration checkout procedures . . . . . . . . . . . . . . . . . . . . . 6-91
iv CIC Pro™ 2026419-033E
7 Checkout procedures . . . . . . . . . . . . . . . . . . . . . . . . 7-1
Safety tests and checkout procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2
Test equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-2
Configuration checkout procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3
Check the unit defaults . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3
Check status of installed printers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3
View system information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-3
Check operation of the secondary display . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
Check mirror configuration . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
Check the status of installed licenses . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-4
Verify settings with Check Centrals command . . . . . . . . . . . . . . . . . . . . . 7-5
Check and configure the speaker volume . . . . . . . . . . . . . . . . . . . . . . . . . 7-5
Check operation of audible alarm tones . . . . . . . . . . . . . . . . . . . . . . . . . . 7-7
Check access to all other care units . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-7
Check the operation of the Citrix application viewed at the CIC Pro center 7­7
Check the hospital intranet browser functionality . . . . . . . . . . . . . . . . . . . 7-7
Check the status of locked beds . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-7
Check the language settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-7
Check the pressures unit-of-measure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-8
Check the custom groupings for patient data . . . . . . . . . . . . . . . . . . . . . . 7-8
Check the shortcuts to favorite CIC Pro center views . . . . . . . . . . . . . . . . 7-8
Check MultiKM (Multimouse) operation . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-8
Check current system settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-8
Check full disclosure license type for all admitted in-unit beds . . . . . . . . . 7-9
Check full disclosure report printing . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-9
Save backup defaults file on the USB memory stick . . . . . . . . . . . . . . . . 7-10
FRU checkout procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-10
Check read and write integrity of hard drive and solid state flash drive . 7-10
Check USB devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-11
Check internal hardware temperature and voltage status . . . . . . . . . . . . 7-12
Check COMM ports . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-13
Check BIOS information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-13
Check drive operation information (Flash drive and hard drive) . . . . . . . 7-14
Check audio component operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-16
Check speaker status . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-17
Check operation of the Watchdog countdown function . . . . . . . . . . . . . . 7-18
Check processor fan status . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-19
Check video function and status of video card and drivers . . . . . . . . . . . 7-19
Check integrity of system files . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-20
Check asset information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 7-21
Check successful execution of Log File Compression Configuration Utility 7­21
8 Troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-1
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-2
2026419-033E CIC Pro™ v
Required tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-2
Tips . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-2
Error messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-2
Display issues . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8
Blank screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8
Blue screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-8
Red screen . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
Incorrect colors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
Browser connectivity issues . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
Printer issues. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
Laser printer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-9
Digital display writer . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-10
MultiKM issues. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-10
License activation failures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-10
CIC Pro center setup issues. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11
Unable to communicate with a device . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-11
List full disclosure beds . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-12
Set full disclosure mode . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-13
Ping full disclosure server . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-14
Display current system settings . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-14
Enable alarms . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-15
Admit Request Info button . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-15
Display waveform indicators . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-15
Require age selection for admit . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-16
Licensing issues. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-16
Time zone, daylight saving time setting, and network time issues . . . . . 8-19
PDF file access from MUSE . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-19
Environment Monitor messages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-19
Log files . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-20
Download log files . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-20
Access current log files . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-21
Application logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-23
Operating system event logs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-24
Operating system Dr. Watson log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-25
Webmin action log . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-25
Access additional runtime diagnostic information . . . . . . . . . . . . . . . . . . 8-26
Device driver information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-26
Network information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-26
Operating system runtime statistics . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-27
Operating system service process information . . . . . . . . . . . . . . . . . . . . 8-28
Process information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-28
Time zone information . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-29
SMART drive status . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 8-29
vi CIC Pro™ 2026419-033E
Perform safe restart of the CIC Pro center . . . . . . . . . . . . . . . . . . . . . . . . . 8-30
Perform safe shutdown of the CIC Pro center . . . . . . . . . . . . . . . . . . . . . . 8-31
Change the logon password for Webmin . . . . . . . . . . . . . . . . . . . . . . . . . . 8-32
9 Field replaceable units (FRUs) . . . . . . . . . . . . . . . . . 9-1
Exploded views . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2
Desktop . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-2
Rack-mount . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-4
Interconnect diagram . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-6
FRUs . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-6
Disaster recovery software kit and Service Tools CD . . . . . . . . . . . . . . . . . 9-6
Accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-6
Power cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-7
Keyboard kits . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-8
Replacement procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-8
Desktop assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-9
Rack-mount assembly . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-10
Common replacement procedures. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-11
Replacing the CPU PCB (mother board) . . . . . . . . . . . . . . . . . . . . . . . . . 9-14
Replacing the CPU battery . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-15
Replacing the hard drive . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-17
Replacing the flash drive . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-18
Replacing the SATA drive cables . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-19
Replacing the power supply . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-20
Replacing the fan . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-21
Replacing the dual speakers . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-22
Replacing the fuse . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-22
Replacing the front bezel . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-23
Re-assemble the cover. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 9-24
10 Preventive maintenance . . . . . . . . . . . . . . . . . . . . . 10-1
Maintenance schedule . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-2
Checklist . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-2
Visual inspection . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-3
Cleaning . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-3
Power source tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-6
Power outlet test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-6
Power cord and plug test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-6
2026419-033E CIC Pro™ vii
Electrical safety tests . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-6
Ground (earth) integrity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-6
Ground (earth) wire leakage current test . . . . . . . . . . . . . . . . . . . . . . . . . 10-7
Enclosure leakage current test . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-8
Test completion . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-10
Check the operation of input devices and displays . . . . . . . . . . . . . . . . 10-10
Perform checkout procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-10
System resource indicator . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-11
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-11
Resource indicator messages when hovering over icon . . . . . . . . . . . . 10-12
Resource indicator messages when icon is double-clicked . . . . . . . . . 10-12
Resource indicator messages from Environment Monitoring Service . . 10-12
System resource restart procedure . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-13
Access log files . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 10-14
11 Reload software . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-1
Purpose . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-2
Process overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-2
Gather required equipment and tools . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-2
Create a CIC Pro center image restore USB memory stick . . . . . . . . . . . 11-2
Reload CIC Pro center software . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-5
Complete checkout procedures. . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-7
Confirm images restored to correct drives . . . . . . . . . . . . . . . . . . . . . . . . 11-7
Complete FRU checkout procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-7
Check proper operation . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-8
Reload process troubleshooting . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-8
Incorrect boot order . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 11-8
Software image on USB stick does not match hardware . . . . . . . . . . . . 11-9
12 Upgrade software . . . . . . . . . . . . . . . . . . . . . . . . . . 12-1
Overview . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-2
Establish alternate monitoring methods . . . . . . . . . . . . . . . . . . . . . . . . . . 12-3
Gather the required equipment . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-3
Prepare the CIC Pro center . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-3
Prepare the service PC . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-4
Connect the service PC to the CARESCAPE Network IX network . . . . . 12-4
viii CIC Pro™ 2026419-033E
Start the software transfer utility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-4
Enter the CARESCAPE Network IX network addresses of CIC Pro centers to
be updated . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-5
Install the software on the target CIC Pro centers . . . . . . . . . . . . . . . . . . 12-6
Activate the software packages . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-8
Complete the checkout procedures . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . 12-9
A Electromagnetic compatibility . . . . . . . . . . . . . . . . .A-1
Electromagnetic compatibility (EMC) . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-2
Guidance and manufacturer’s declaration . . . . . . . . . . . . . . . . . . . . . . . . . A-2
Electromagnetic emissions . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A-2
Electromagnetic immunity . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .A-3
Recommended separation distances . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-5
Compliant cables and accessories . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . A-6
B Backup and restore - backed up data modules . . . B-1
Data module detail . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . B-2
C Device compatibility . . . . . . . . . . . . . . . . . . . . . . . . . C-1
CIC Pro center v5.1.x compatibility . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . C-2
Central stations . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .C-2
Telemetry devices . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .C-2
Bedside monitors . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .C-2
Other GE systems . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . . .C-3
2026419-033E CIC Pro™ ix
x CIC Pro™ 2026419-033E
1

Introduction

2026419-033E CIC Pro™ 1-1
Introduction

Equipment information

License agreement

It is important that you carefully read the terms and conditions of this license agreement before commencing the use of the clinical information center workstation (the “workstation”) and the clinical information center program recorded therein and any accompanying user documentation (“program”). This license represents the entire license agreement concerning the program between you and GE and supersedes all other communications or advertising related to the program except any terms and conditions of sale or warranties or warranty limitations relative to the program and/or the workstation as may be embodied in any documentation supplied with the workstation. By commencing the use of the workstation and the program contained therein, you are accepting and agreeing to be bound by all the terms and conditions of this license agreement. If you are not willing to be bound by the terms and conditions of this license agreement, you should promptly return the workstation to GE and you will receive a refund of the purchase price.
I. Grant
II. Royalty
III. Limitations
The Program is capable of coupling one to sixteen patient monitoring units to the Workstation. GE hereby grants you a non-exclusive, non-transferable right and license to use the Program for couplin g the number of patient monitoring units to th e Workstation for which a per-unit royalty has been paid pursuant to Article II hereof.
You have paid GE a one-time, per-unit royalty equal to GE Medical Systems Information T echnologies, Inc.’s current published price for the use of the Program. The per-unit royalty is based on the actual number of patient monitors intended to be coupled by the Program to the Workstation as stated in the Purchase Order for the Workstation and the Program. If you use the Program to couple any patient monitoring units to the Workstation in addition to the number for which a per unit royalty was previously paid, you agree to pay GE an additional per-unit royalty equal to GE Medical Systems Information Technologies, Inc.’s then current published royalty for the Program for each such additional patient monitoring unit so coupled. The additional per-unit royalty shall be paid to GE within 30 days of the use of the Program to couple any such additional patient monitoring units to the Workstation.
You hereby agree not to: (1) use the Program in any network or system other than to couple patient monitoring units to the Workstation; (2) make any copy of the Program for any reason, or allow or assist others to do so; (3) modify, reverse engineer, de­compile or disassemble the Program or merge any part of the Program into any other program; (4) rent, sell, sublease, assign, transfer or otherwise share the Program or any of your rights in the Program under this Agreement with any third party; or, (5) remove or alter any copyright notice, labels or trademarks from the Program or the Workstation.
1-2 CIC Pro™ 2026419-033E
IV. Title
This License is not a sale. Title and all copyrights to the Program and any copy made by you remains the sole property of GE.
V. Term
This Agreement shall continue in force until terminated. This Agreement shall terminate automatically when you cease using the Workstation and the Program for their intended purpose. GE may terminate this Agreement on 30 days written notice if you make any unauthorized copies of the Program or fail to comply with any of the restrictions on use of the Program as set forth herein.
VI. Limited warranty, disclaimer and limitation of liability
A. Licensor warrants that on the acceptance date the Program shall be free from significant programming errors and shall op erate and con form to the published functional specifications applicable thereto, and that the Program shall conform to the standards generally observed in the industry for similar software.
Introduction
VII. Governing law
B. This warranty shall be invalidated by your modification of the Program if such modification or the interaction between such modification and the Program as supplied by GE is the cause of the defect, error or non-conformity.
C. Except as stated above, the warranty covering the Program and the Workstation shall be either GE Standard Warranty or Limited Extended Parts Warranty as published by GE and hereby made a part hereof.
D. Except for the express warranties stated herein, GE disclaims all warranties with regard to the program including implied warranties of merchantability or fitness for a particular purpose.
E. GE Medical Systems Information Technologies, Inc.’ s entire liability to you arising out of or in connection with this Agreement shall not exceed the per-unit royalty paid to GE for use of the Program. You acknowledge that the amount paid to GE for use of the Program is insufficient for GE to undertake any greater risk. In no event shall GE be liable for any indirect, incidental, consequential, special or exemplary damages (including without limitation, lost profits, business interruption , lo ss of business information, personal injury or any other pecuniary loss) arising from the use of the program, even if GE has been advised of the possibility of such damages.
This Agreement shall be governed by the laws of the State of Wisconsin.
VIII. Partial invalidity
If any provision of this Agreement is held invalid or unenforceable, the remaining portions of the Agreement shall continue in full force and effect.
2026419-033E CIC Pro™ 1-3
Introduction

Intended use of the equipment

The CIC Pro Clinical Information Center central station is intended for use under the direct supervision of a licensed healthcare practitioner. The intended use is to provide clinicians with adult, pediatric and neonatal patient data in a centralized location within a hospital or clinical environment.
CIC Pro Clinical Information Center central station is intended to collect information from a network and display this data. This data includes physiological, patient demographic and/or other non-medical information. Physiological parameters and waveforms from monitors and telemetry systems can be displayed and printed from the CIC Pro Clinical Information Center central station. Beat to beat patient information for all parameters and waveforms from the bedside and telemetry systems can be displayed.
The CIC Pro Clinical Information Center central station supports the ability to access information from the CIC Pro Clinical Information Center central stations’ products in a web browser format. Additionally, the CIC Pro Clinical Information Center central station supports the ability to access patient information collected from the unity network and stored on a network server.

Safety information

Dangers
Warnings
The terms danger, warning, and caution are used throughout this manual to point out hazards and to designate a degree or level of seriousness. Familiarize yourself with their definitions and significance.
Hazard is defined as a source of potential injury to a person. Danger indicates an imminent hazard, which, if not avoided, will result in death
or serious injury.
Warning indicates a potential hazard or unsafe practice, which, if not avoided,
could result in death or serious injury.
Caution indicates a potential hazard or unsafe practice, which, if not avoided,
could result in minor personal injury or product/property damage.
Note provides application tips or other useful information to assure that you get
the most from your equipment.
No danger statements apply to this product.
The following warnings apply to this product.
1-4 CIC Pro™ 2026419-033E
Introduction
WARNING
ELECTRIC SHOCK— To avoid electric shock, the CIC Pro center and its accessories should not be placed within the patient environment, which is a volume related to an object (bed, chair, table, treadmill, etc.) where a patient is intended to be diagnosed, monitored, or treated.
WARNING
ACCESSORIES (SUPPLIES) — To ensure patient safety, use only parts and accessories recommended by GE.
WARNING
ACCIDENTAL SPILLS — To avoid electric shock or device malfunction, liquids must not be allowed to enter the device. If liquids have entered a device, take it out of service and have it checked by a service technician before it is used again.
WARNING
ACCURACY — If the accuracy of any value displayed on the screen or printed on a graph strip is questionable, first determine the patient's vital signs by alternative means. Then, verify the CIC Pro center and printer are working correctly.
WARNING
ALARMS — Do NOT rely exclusively on the audible alarm system for Bedside Monitoring. Adjustment of CIC Pro center alarm volume to a low level or OFF during Bedside Monitoring may result in inability to hear the alarm and a hazard to the patient. Remember that the most reliable method of Bedside Monitoring combines close personal surveillance with correct operation of monitoring equipment.
After connecting the monitor to the central station and/or nurse­alert, verify the function of the alarm system. Repeat this verification periodically, including a check of all connected speakers.
CIC Pro center audible alarms will not sound for patients with bedside monitoring devices configured to “Operating Room” mode.
The functions of the alarm system for monitoring of the patient must be verified at regular intervals. Check speaker volume periodically to ensure audio alarm functionality.
2026419-033E CIC Pro™ 1-5
Introduction
WARNING
BEFORE USE — Before putting the system into operation, visually inspect all connecting cables for signs of damage. Damaged cables and connectors must be replaced immediately.
Before using the system, the operator must verify that it is in correct working order and operating condition.
Periodically, and whenever the integrity of the product is in doubt, test all functions.
WARNING
DISCONNECTION FROM MAINS — When disconnecting the system from the power line, remove the plug from the wall outlet first. Then you may disconnect the power cord from the device. If you do not observe this sequence, there is a risk of coming into contact with line voltage by inserting metal objects, such as the pins of leadwires, into the sockets of the power cord by mistake.
WARNING
DISPOSAL — Dispose of the packaging material, observing the applicable waste control regulations and keeping it out of children’s reach.
WARNING
EXPLOSION HAZARD — Do not use this equipment in the presence of flammable anesthetics, vapors or liquids.
WARNING
INTERFACING OTHER EQUIPMENT — Devices may only be interconnected with each other or to parts of the system when it has been determined by qualified biomedical engineering personnel that there is no danger to the patient, the operator, or the environment as a result. The devices must comply with relevant IEC and ISO safety standards.
Safe and proper operation should be verified with the applicable manufacturer’s instructions for use.
WARNING
NETWORK INTEGRITY — The CIC Pro center can reside on the hospital’s computer network, and it is possible that inadvertent or malicious network activity could adversely affect patient monitoring. The integrity of the computer network is the responsibility of the hospital.
1-6 CIC Pro™ 2026419-033E
Cautions
Introduction
The following cautions apply to this product.
CAUTION
EMC — 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 monitor comply with the relevant EMC requirements. X-ray equipment or MRI devices are a possible source of interference as they may emit higher levels of electromagnetic radiation.
CAUTION
EMC — 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 monitor comply with the relevant EMC requirements. X-ray equipment or MRI devices are a possible source of interference as they may emit higher levels of electromagnetic radiation.
Changes or modifications to this device/system not expressly approved by GE may cause EMC issues with this or other equipment. This device/system is designed and tested to comply with applicable standards and regulations regarding EMC and needs to be installed and put into service according to the EMC information stated as follows:
Use of known RF sources, such as cell/portable phones, or other radio frequency (RF) emitting equipment near the system may cause unexpected or adverse operation of this device/system. Consult qualified personnel regarding device/system configuration.
The device/system should not be used adjacent to, or stacked with, other equipment. If adjacent or stacked use is necessary, the device/ system should be tested to verify normal operation in the configuration in which it is being used. Consul t quali fied personnel regarding device/system configuration.
The use of accessories, transducers and cables other than those specified may result in increased emissions or decreased immunity performance of the device/system.
This device/system is suitable for use in all establishments other than domestic and those directly connected to the public low-voltage power supply network that supplies buildings used for domestic purposes. Mains power should be that of a typical commercial or hospital environment.
Refer to the electromagnetic compatibility and guidelines in the service manual for additional compliance and safety info rmation.
2026419-033E CIC Pro™ 1-7
Introduction
CAUTION
NEGLIGENCE — GE does not assume responsibility for damage to the equipment caused by improperly vented cabinets, improper or faulty power, or insufficient wall strength to support equipment mounted on such walls.
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 USA, if the installation of the equipment will use 240V rather than 120V, the source must be a center-tapped, single-phase circuit.
This equipment is suitable for connection to public mains as defined in CISPR11/EN55011.
CAUTION
RESTRICTED SALE — U.S. federal law restricts this device to be sold by or on the order of a physician.
CAUTION
SECURITY — The web browser which runs in conjunction with the CIC Pro center is intended for hospital intranet use only. If confidential patient information is made available from the hospital intranet, the security of the data is the responsibility of the hospital.
CAUTION
SUPERVISED USE — This equipment is intended for use under the direct supervision of a licensed health care practitioner.
CAUTION
During shutdown or while in administrator mode, beds displayed by the CIC Pro center will be unmonitored if not displayed by a different CIC Pro center.
Notes
The following notes apply to this product.
NOTE
This device is not intended for home use.
1-8 CIC Pro™ 2026419-033E
NOTE
Parts and accessories used must meet all local building and safety requirements.
NOTE
Patient environment is any volume in which intentional or unintentional contact can occur between the patient and parts of the system or between the patient and other persons touching parts of the system (IEC 60601-1-1).

Equipment symbols

NOTE
Some symbols may not appear on all equipment.
Symbol Description
ATTENTION: Consult accompanying documents.
Introduction
TYPE B APPLIED PART: Non-isolated applied part suitable for intentional external and internal application to the patient excluding direct cardiac application.
[Medical Standard Definition:] Applied part complying with the specified requirements of IEC 60601-1 Medical Standards to provide protection against electric shock, particularly regarding allowable leakage current.
TYPE BF APPLIED PART: Isolated (floating) applied part suitable for intentional external and internal application to the patient excluding direct cardiac application. “Paddles” outside the box indicate the applied part is defibrillator proof.
[Medical Standard Definition:] F-type applied part (floating/isolated) complying with the specified requirements of IEC 60601-1 Medical Standards to provide a higher degree of protection against electric shock than that provided by type B applied parts.
NOTE
The rating of protection against electric shock (indicated by symbol for CF or BF) is achieved only when used with patient applied parts recommended by GE.
TYPE CF APPLIED PART: Isolated (floating) applied part suitable for intentional external and internal application to the patient including direct cardiac application. “Paddles” outside the box indicate the applied part is defibrillator proof.
[Medical Standard Definition:] F-type applied part (floating/isolated) complying with the specified requirements of IEC 60601-1 Medical Standards to provide a higher degree of protection against electric shock than that provided by type BF applied parts.
Writer door button.
Silence Alarm keyboard key.
CE mark.
2026419-033E CIC Pro™ 1-9
Introduction
Symbol Description
This symbol indicates the date of manufacture of this device. The first four digits identify the year and the last two digits identify the month.
Fuse. Replace the fuse with a fuse of the same type and rating.
Power On and Off.
Medical Equipment. With Respect to Electric Shock, Fire and Mechanical Hazards Only, In Accordance with UL 60601-1, CAN/CSA C22.2 NO.601.1, and IEC 60601-1.
For Russia only: Russian GOST-R certification.
USB connector port.
Ethernet connector port used to connect to the CARESCAPE Network (MC or IX network) as indicated on the device.
Serial connector ports 1 and 2.
Digital Visual Interface - Integrated for primary video connection that supports digital and analog displays.
Digital Visual Interface - Digital for secondary video connection that supports digital displays only.
Speaker out connector port.
Power indicator.
1-10 CIC Pro™ 2026419-033E
Symbol Description
This symbol indicates that the waste of electrical and electronic equipment must not be disposed as unsorted municipal waste and must be collected separately. Please contact the manufacturer or other authorized disposal company to decommission your equipment.
European authorized representative.
Manufacturer name and address.
Equipotential stud. A ground wire from another device can be tied here to ensure the devices share a common reference point.
NOTE
The following symbols (required by China law only) are representative of what you may see on your equipment.
Introduction
The number in the symbol indicates the EFUP period in years, as explained below. Check the symbol on your equipment for its EFUP period.
This symbol indicates the product contains hazardous materials in excess of the limits established by the Chinese standard SJ/T11363-2006 Requirements for Concentration Limits for Certain Hazardous Substances in Electronic Information Products. The number in the symbol is the Environment-friendly User Period (EFUP), which indicates the period during which the toxic or hazardous substances or elements contained in electronic information products will not leak or mutate under normal operating conditions so that the use of such electronic information products will not result in any severe environmental pollution, any bodily injury or damage to any assets. The unit of the period is “Year”.
In order to maintain the declared EFUP, the product shall be operated normally according to the instructions and environmental conditions as defined in the product manual, and periodic maintenance schedules specified in Product Maintenance Procedures shall be followed strictly.
Consumables or certain parts may have their own label with an EFUP value less than the product. Periodic replacement of those consumables or parts to maintain the declared EFUP shall be done in accordance with the Product Maintenance Procedures. This product must not be disposed of as unsorted municipal waste, and must be collected separately and handled properly after decommissioning.
This symbol indicates that this electronic information product does not contain any toxic or hazardous substance or elements above the maximum concentration value established by the Chinese standard SJ/T1 1363-2006, and can be recycled after being discarded, and should not be casually discarded.

Service requirements

Follow the service requirements listed below, and in the Preventive maintenance chapter of this manual.
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.
2026419-033E CIC Pro™ 1-11
Introduction
### ## ## #### # #
123456
Failure on the part of the responsible individual, hospital, or institution using this
equipment to implement a satisfactory maintenance schedule may cause undue equipment failure and possible health hazards.
Regular maintenance, irrespective of usage, is essential to ensure that the
equipment is always functional when required.

Manufacturer responsibility

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.

Equipment identification

Every GE device has a unique serial number for identification. A sample of the information found on a serial number label is shown below.
1
Product code
1
2 Year manufactured 3 Fiscal week manufactured 4 Production sequence number 5 Manufacturing site 6 Miscellaneous characteristic
1
The product code is:
SDY for the MP100D (desktop model) platform SDZ for the MP100R (rack-mounted mode l) plat form
1-12 CIC Pro™ 2026419-033E

Manual information

Manual purpose

This manual supplies technical information for service representatives and technical personnel so they can maintain the equipment to the assembly level. Use it as a guide for maintenance and electrical repairs considered field repairable. Where necessary, the manual identifies additional sources of relevant information and technical assistance.

Intended audience

This manual is intended for use by service representatives and technical personnel who maintain, troubleshoot, or repair the equipment.

Related manuals

Introduction

Conventions used

Equipment terms
Critical Care Monitoring Clinical Reference and Troubleshooting Guide CIC Pro™ Clinical Information Center Operator’s Manual CIC Pro™ Clinical Information Center Technical Specifications Supplement
MP100 Series
This manual uses the following terms to simplify common equipment names.
Term Description
MC network Refers to the CARESCAPE Network MC network. IX network Refers to the CARESCAPE Network IX network. CIC Pro center Refers to the CIC Pro Clinical Information Center. CIC Pro Refers to the CIC Pro Clinical Information Center. Flash drive Solid-state drive. Telemetry Server Refers to the ApexPro Telemetry Server/Tower. Transmitter/transceiver Refers to an Apex, ApexPro or ApexPro CH transmitter or
ApexPro FH transceiver.
USB memory stick A memory data storage device which is used to create an
image to restore the CIC Pro center software and to activate CIC Pro center licenses.
Writer Refers to the PRN 50-M digital writer.
2026419-033E CIC Pro™ 1-13
Introduction
Text styles
Illustrations and names
This manual uses the following text styles to identify hardware terms, software terms and the correct way to enter data.
Style Definition
Bold Indicates hardware items, such as keys, labels or connectors.
Bold and italicized Indicates software items, such as menus, menu options or
screen text. Italics Emphasizes a word. > Indicates menu options or control settings to select
consecutively. + Indicates keyboard keys to select simultaneously.
In this manual, all illustrations are provided as examples only. They may not necessarily reflect your monitoring setup or data viewed on your monitoring device.

Ordering manuals

Revision history

All names appearing in examples and illustrations are fictitious. The use of any real person’s name is purely coincidental.
A paper copy of this manual will be provided upon request. Contact your local GE representative and request the part number on the first page of the manual.
Each page of this document has the document part number and revision letter at the bottom of the page. The revision letter changes whenever the document is updated.
Revision Comments
A Release of CIC Pro v5.1. B Updated Warnings and the Set up a mirror CIC Pro center
section. C Updated for Log Compression Configuration Utility. D Updated for new printer. E Updated the section on configuring the NO COMM alarm
setting.
1-14 CIC Pro™ 2026419-033E
2

Equipment overview

2026419-033E CIC Pro™ 2-1
Equipment overview
1
2
3
4

Standard components

NOTE
The Unity Network has been renamed to the CARESCAPE Network. Not all references to the Unity Network will be changed immediately; Unity may appear in some places and CARESCAPE in others. It is important to understand that while the CARESCAPE Network replaces the Unity Network name, they refer to the same GE monitoring network
Standard components include the following items:
Processor box Primary display External speakers Standard keyboard and mouse
2-2 CIC Pro™ 2026419-033E
Item Function
1 Processor box Run the CIC Pro center application. 2 Primary display Display real-time and stored patient data,
control windows, and various system level operations. Can display 16 patients simultaneously.
3 Standard mouse and keyboard Enter data, navigate menus, and choose
options.
4 External speakers Sound audible patient status and system
status alarm tones.
022B

Display

14
Front view
1 2
3 4
5
6
7
9
8
10
11
12
13
Back view
18

Processor box

Desktop views
Equipment overview
You can configure the CIC Pro center to display real-time parameter waveforms and numeric data for one to 16 patients. See Set the Display Configuration (non-mirror
CIC Pro centers) on page 6-49.
You can also view stored parameter waveforms and numeric data, control windows, and various system level operations.
The processor box runs the CIC Pro center application. It can be ordered as a desktop server (MP100D) or as a rack-mounted server (MP100R) and has the following connectors, ports, and switches. For information on USB extender limitations, see
Restrictions on page 5-11.
2026419-033E CIC Pro™ 2-3
Equipment overview
16
Side view
3 4
5
6
7
8
9
10
11
14
Front view
16
17
1
2
12
13
15
Back view
Rack-mount views
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