1-2 Patient Data Module 2030047-001A
Introduction
Manual information
Revision history
Each page of this manual has the document part number and revision letter at the
bottom of the page. The revision letter identifies the document’s update level. The
revision history of this document is summarized below.
Manual purpose
This manual provides technical information for service representatives and technical
personnel for maintaining the equipment.
Intended audience
This manual is intended for service representatives and technical personnel who
install, configure, maintain, administer, troubleshoot, or repair this equipment.
Ordering manuals
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.
Safety information
Responsibility of the manufacturer
GE is responsible for the effects of safety, reliability, and performance only if:
Assembly operations, extensions, readjustments, modifications, or repairs are
carried out by persons authorized by GE.
The electrical installation of the relevant room complies with the requirements of
the appropriate regulations.
The equipment is used in accordance with the instructions for use.
Intended use
This device is intended for use under the direct supervision of a licensed health care
practitioner.
This device is not intended for home use.
Federal law restricts this device to be sold by or on the order of a physician.
Revision Comments
A Initial release.
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