Biowave BiowavePENS, Руководство пользователя

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BiowavePRO
®
User’s Manual
Biowave Corporation 102
The BiowavePRO
®
Neurostimulator is intended for use in the electromagnetic
environment specified below. The customer or the user of the BiowavePRO
Neurostimulator should assure that it is used in such an environment.
±6 kV contact
±8 kV air
Not applicable
±6 kV contact
±8 kV air
±2 kV for power
supply lines
±1 kV for input/
output lines
<5% U
T
(>95% dip
in U
T
) for 0.5 cycle
40% U
T
(60% dip in
U
T
) for 5 cycles
70 % U
T
(30% dip
in U
T
) for 25 cycles
<5% U
T
(>95% dip
in U
T
) for 5 sec
3 A/m
Electrostatic
discharge (ESD)
IEC 61000-4-2
Electrical fast
transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage
dips, short
interruptions
and voltage
variations on
power supply
input lines
IEC 61000-4-11
Immunity test IEC 60601
test level Compliance
level
Guidance and Manufacturer’s Declaration – Electromagnetic Immunity
Electromagnetic
environment – guidance
Floors should be wood,
concrete or ceramic tile. If floors
are covered with synthetic
material, the relative humidity
should be at least 30%.
Mains power quality
should be that of a typical
commercial or hospital
environment.
Power frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
±1 kV differential
mode
±2 kV common
mode
Not applicable Mains power quality
should be that of a typical
commercial or hospital
environment.
Not applicable Mains power quality
should be that of a typical
commercial or hospital
environment.
3 A/m Power frequency magnetic
fields should be at levels
characteristic of a typical
location in a typical
commercial or hospital
environment.
NOTE: U
T
is the A.C. mains voltage prior to application of the test level.