Biocompatibility - GE SEER 1000 Operating Manual

Ecg recorder and mobile application
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Introduction
Radio Frequency (RF) devices may interfere with the use or accuracy of
the device or system. When installing or using the device or system, be
aware of the proximity of known RF sources, such as:
Radio and TV stations
Portable and mobile RF communication devices (cell phones, two-way
radios)
X-ray, CT, or MRI devices.
These devices are also possible sources of interference as they may
emit higher levels of electromagnetic radiation.
WARNING
EQUIPMENT MALFUNCTION — Use of portable phones or other radio fre-
quency (RF) emitting equipment near the system may cause unexpected
or adverse operation.
Do not use unauthorized portable phones or other electronic equipment
that may emit radio frequency (RF) near this system.
WARNING
ACCESSORIES/COMPONENTS — Adding accessories or components, or
modifying the medical device or system, may result in increased EMIS-
SIONS or decreased IMMUNITY of the device or system.
Use the following resources for more information on EMI/EMC and RF
concerns:
The Supplies and Accessories Reference Guide for your system
GE Healthcare or GE Healthcare authorized representatives
The Electromagnetic Compatibility appendix in this operator's manual

Biocompatibility

The parts of the system described in this manual, including all accessories
that come into contact with the patient during the intended use, fulfill the
biocompatibility requirements of the applicable standards. If you have
questions in this matter, contact your GE Healthcare representative.
18
SEER™ 1000
2067634-077 Revision B

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