Verity Medical NeuroTrac IFC Rehab Operation Manual page 32

Table 201:
The NeuroTrac™ product is intended for use in the electromagnetic environ�
ment specified below. The customer or the user of the The NeuroTrac™ product
should ensure that it is used in such environment
Emission test
RF emission
CISPR 11
RF emission
CISPR 11
Harmonic emissions
IEC 61000�3�2
Voltage fluctuations/
flicker emissions
IEC 61000�3�3
Table 202:
The NeuroTrac™ product is intended for use in the electromagnetic environ�
ment specified 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
Electrostatic
discharge (ESD)
IEC 61000�4�2
Power frequency
(50/60 Hz)
magnetic field
IEC 61000�4�8
Guidance and manufacturer's declaration
� electromagnetic emission
Compliance
Group 1
Class B
Not applicable
Not applicable
Guidance and manufacturer's declaration
– electromagnetic immunity
IEC 60601
test level
6 kV contact ±6 kV contact
±8 kV air ±8 kV air
3 A/m 3 A/m
NeuroTrac™ IFC Rehab Operation Manual
Electromagnetic environment guid-
The NeuroTrac™ product uses RF energy
only for its internal function.
emissions are very low and are not likely to
cause any interference in nearby electronic
equipment
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
Compliance Electromagnetic environ-
level
Floors should be wood, con�
crete or ceramic tile. If floors are
covered with synthetic material,
the relative humidity should be
at least 30 %.
Power frequency magnetic
fields should be at levels char�
acteristic of a typical location in
a typical commercial or hospital
environment.
32
ance
Therefore, its RF
ment guidance