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.
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.
1-2CIC 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.
2026419-033ECIC 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.
1-4CIC 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.
2026419-033ECIC 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.
1-6CIC 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.
2026419-033ECIC 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.
1-8CIC 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.
SymbolDescription
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.
2026419-033ECIC Pro™1-9
Introduction
SymbolDescription
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.
1-10CIC Pro™2026419-033E
SymbolDescription
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.
2026419-033ECIC 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
2Year manufactured
3Fiscal week manufactured
4Production sequence number
5Manufacturing site
6Miscellaneous characteristic
1
The product code is:
SDY for the MP100D (desktop model) platform
SDZ for the MP100R (rack-mounted mode l) plat form
1-12CIC 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.
TermDescription
MC networkRefers to the CARESCAPE Network MC network.
IX networkRefers to the CARESCAPE Network IX network.
CIC Pro centerRefers to the CIC Pro Clinical Information Center.
CIC ProRefers to the CIC Pro Clinical Information Center.
Flash driveSolid-state drive.
Telemetry ServerRefers to the ApexPro Telemetry Server/Tower.
Transmitter/transceiverRefers to an Apex, ApexPro or ApexPro CH transmitter or
ApexPro FH transceiver.
USB memory stickA 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.
WriterRefers to the PRN 50-M digital writer.
2026419-033ECIC 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
BoldIndicates hardware items, such as keys, labels or connectors.
Bold and italicizedIndicates software items, such as menus, menu options or
screen text.
ItalicsEmphasizes 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.
RevisionComments
ARelease of CIC Pro v5.1.
BUpdated Warnings and the Set up a mirror CIC Pro center
section.
CUpdated for Log Compression Configuration Utility.
DUpdated for new printer.
EUpdated the section on configuring the NO COMM alarm
setting.
1-14CIC Pro™2026419-033E
2
Equipment overview
2026419-033ECIC 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
2-2CIC Pro™2026419-033E
ItemFunction
1Processor boxRun the CIC Pro center application.
2Primary displayDisplay real-time and stored patient data,
control windows, and various system level
operations. Can display 16 patients
simultaneously.
3Standard mouse and keyboardEnter data, navigate menus, and choose
options.
4External speakers Sound audible patient status and system
status alarm tones.
022B
Display
14
Front view
12
34
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.
2026419-033ECIC Pro™2-3
Equipment overview
16
Side view
34
5
6
7
8
9
10
11
14
Front view
16
17
1
2
12
13
15
Back view
Rack-mount views
2-4CIC Pro™2026419-033E
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