CARESCAPE Central Station: Technical Specifications Supplement
CARESCAPE Central Station: Technical Specifications Supplement
2048001-130B
© 2016 General Electric Company
All rights reserved.
The information in this manual applies to the software version and product models on the first page of the manual. Due to continuing
innovation, specifications in this manual are subject to change without notice.
For technical documentation purposes, the abbreviation GE is used for the legal entity name, GE Medical Systems Information Technologies,
Inc., and GE Healthcare Finland Oy.
GE, GE Monogram, APEX, APEXPRO, and CARESCAPE are trademarks of General Electric Company.
12RL, Aware, CIC Pro, DASH, DINAMAP, MARS, MUSE, SOLAR, TRAM, and UNITY NETWORK are trademarks of GE Medical Systems Information
Technologies, Inc.
Mobile Viewer is a trademark of GE Healthcare Finland Oy.
Java Powered. Java and all Java based trademarks and logos are trademarks or registered trademarks of Oracle America, Inc. in the U.S.
and other countries.
All third party trademarks are the property of their respective owners.
Due to continual product innovation, design and specifications for this product are
subject to change without notice. Availability of some features is dependent on the
monitoring devices in use. Additionally, some features may only be available when an
optional license is purchased.
General specifications
Item Description
Multi-Viewer ● Displays parameter numerics and waveforms for up to
16 patients at a time.
● Displays up to four waveforms per patient.
● To select large or small font for secondary parameter
numerics.
● Matches parameter numerics color to waveform color.
Single Viewer ● Displays parameter numerics, waveforms, historical
data for one patient at a time.
● Displays up to nine waveforms per patient.
● Temporarily displays an additional (17th) patient.
● Provides option to create Save As Favorite buttons to
quickly access frequently used screen formats.
Graphic Trends ● Displays parameter data over a period of time in a
graphical format, including AFIB trending with select
monitoring devices.
● Displays arrhythmia alarm trend as vertical bars at the
time of occurrence.
● Displays up to:
■ Six parameters in half screen format.
■ Twelve parameters in full-screen format.
● Defines up to 12 trend groups for customized trend
views.
Display specifications
Item Description
Display size 54.61 cm (21.5 in)
Resolution 1920 x 1080 pixels
Refresh rate 60 Hz
● Horizontal: 178°
Viewing angle
● Vertical: 178°
Touchscreen technology Surface Acoustical Wave (SAW)
Touch interface USB 2.0
Power requirements
Item Description
Voltage 100 - 240 V AC (nominal)
Frequency 50 - 60 Hz (nominal)
Power 100 VA (341 BTU/hr) (maximum)
Physical specifications
Integrated processing unit (MAI700)
Item Description
Height (maximum including
40 cm (15.75 in)
stand)
Width 55.5 cm (21.85 in)
Depth (maximum including
28 cm (11.02 in)
stand)
Weight 12 kg (26 lb 7.2876 oz)
Cooling Convection cooling with heat sink
● Vertical mount with stand
● Wall mount
Mounting
■ Fixed flush mount
■ Tilt and swivel flush mount
● Two DisplayPort output.
● Two network (Ethernet) connection/interfaces.
Connection/interfaces
● Six USB 2.0 (Type A) connection/interfaces.
● Power socket with fuse and switch.
Device classification
The processing unit is afforded the following protection according to its device
classification. All other components (e.g., keyboard and mouse, displays) have the
degree of protection afforded by their device classification. For more information, see
the documentation accompanying the device.
Item Classification
The type of protection against Class I.
electric shock
The degree of protection against Not applicable (no applied parts).
electric shock
The degree of protection against IPX1 (Protection against vertically falling drops of water).
harmful ingress of water
The degree of safety application Equipment is not suitable for use in the presence of
in the presence of a flammable flammable anesthetic mixture with air or oxygen or
anesthetic mixture with air nitrous oxide or within an oxygen-rich environment.
or with oxygen or nitrous
oxide or within an oxygen-rich
environment
Method(s) of sterilization or Not applicable (no applied parts).
disinfection recommended by
the manufacturer
Defibrillator protection Not applicable (no applied parts).
Mode of operation Continuous operation.
Power line connection Not a permanent connection.
Compliance
This device complies with the requirements of the following standards:
● IEC/EN 60601-1
● IEC/EN 60601-1-2
● IEC/EN 60601-1-6
● IEC/EN 60601-1-8
● EN15223
Revision history
The part number and revision letter for this manual are at the bottom of each page.
The revision letter changes whenever the manual is revised. The first letter shown in
this table is the first customer-released version of this manual.
Revision Description
B Initial release.
GE Medical Systems Information Technologies, Inc., a General Electric Company, doing business as GE
Healthcare.
www.gehealthcare.com