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Verity Medical NeuroTrac IFC Rehab Manual de usuario Pagina 32

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NeuroTrac™ IFC Rehab Operation Manual
32
Table 201: Guidance and manufacturer’s declaration
� electromagnetic emission
The NeuroTrac™ product is intended for use in the electromagnetic environ�
ment specied below. The customer or the user of the The NeuroTrac™ product
should ensure that it is used in such environment
Emission test Compliance Electromagnetic environment guid-
ance
RF emission
CISPR 11
Group 1
The NeuroTrac™ product 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 emission
CISPR 11
Class B
The NeuroTrac™ product is suitable for use
in all establishments , including domestic es�
tablishments and those directly connected to
the public low voltage power supply network
that supplies buildings used for domestic
purposes
Harmonic emissions
IEC 61000�3�2
Not applicable
Voltage uctuations/
icker emissions
IEC 61000�3�3
Not applicable
Table 202: Guidance and manufacturer’s declaration
– electromagnetic immunity
The NeuroTrac™ product is intended for use in the electromagnetic environ�
ment specied below. The customer or the user of theNeuroTrac™ product
should assure that it is used in such an environment, and that precautions
regarding that environment are heeded.
Immunity test
IEC 60601
test level
Compliance
level
Electromagnetic environ-
ment guidance
Electrostatic
discharge (ESD)
IEC 61000�4�2
6 kV contact
±8 kV air
±6 kV contact
±8 kV air
Floors should be wood, con�
crete or ceramic tile. If oors are
covered with synthetic material,
the relative humidity should be
at least 30 %.
Power frequency
(50/60 Hz)
magnetic eld
IEC 61000�4�8
3 A/m 3 A/m
Power frequency magnetic
elds should be at levels char�
acteristic of a typical location in
a typical commercial or hospital
environment.
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