Revision C 250cx Series Maternal/Fetal Monitor 1-9
2036947-001
Introduction: Electromagnetic Interference
Electromagnetic Interference
This device has been tested and found to comply with the limits for medical devices to
the IEC 601-1-2:1993, EN60601-1-2:2001, Medical Device Directive 93/42/EEC.
These limits are designed to provide reasonable protection against harmful interference
in a typical medical installation.
However, because of the proliferation of radio-frequency transmitting equipment
and other sources of electrical noise in the health-care and home environments (for
example, cellular phones, mobile two-way radios, electrical appliances), it is
possible that high levels of such interference due to close proximity or strength of a
source, may result in disruption of performance of this device.
Refer to the Electromagnetic Immunity information in this product’s service manual
for EN 60601-1-2 (2001) Edition 2 compliance information and safety information
for this product.
This equipment generates, uses, and can radiate radio frequency energy and, if not
installed and used in accordance with these instructions, may cause harmful
interference with other devices in the vicinity. Disruption or interference may be
evidences by erratic readings, cessation of operation, or incorrect functioning. If this
occurs, the site of use should be surveyed to determine the source of this disruption,
and actions taken to eliminate the source.
The user is encouraged to try to correct the interference by one or more of the
following measures:
Turn equipment in the vicinity off and on to isolate the offending equipment.
Reorient or relocate the other receiving device.
Increase the separation between the interfering equipment and this equipment.
If assistance is required, contact your GE Medical Systems
Information Technologies Service Representative.
To Next Page
Loading...
Need help?
General
