Revision B SEER Light Ambulatory Recorder/Controller B-3
2019818-008
Electromagnetic Compatibility: Electromagnetic Compatibility (EMC)
Electromagnetic Compatibility (EMC)
Changes or modification to this system not expressly approved by GE
Medical System could cause EMC issues with this or other equipment.
This system is designed and tested to comply with applicable regulation
regarding EMC and needs to be installed and put into service according
to the EMC information stated as follows.
WARNING
Use of portable phones or other radio frequency (RF)
emitting equipment near the system may cause
unexpected or adverse operation.
WARNING
The equipment or system should not be used adjacent to,
or stacked with, other equipment. If adjacent or stacked
use is necessary, the equipment or system should be
tested to verify normal operation in the configuration in
which it is being used.
Guidance and Manufacturer’s Declaration – Electromagnetic
Emissions
The SEER Light recorder and controller are intended for use in the
electromagnetic environment specified below. It is the responsibility of
the customer or user to ensure that the SEER Light recorder and
controller are used in such an environment.
Emissions Test Compliance Electromagnetic Environment - Guidance
RF emissions
CISPR11
Group 1
The equipment uses RF energy only for its
internal function. Therefore, its RF emissions
are very low and are not likely to cause any
interference in nearby electronic equipment.
RF emissions
CISPR11
Class A
The equipment is suitable for use in all
establishments including domestic
establishments and those directly connected to
the public low-voltage power supply network
that supplies buildings used for domestic
purposes.
Harmonic Emissions
EN 61000-3-2
Class A
Voltage fluctuations/
Flicker emissions
EN 61000-3-3
Complies
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