Guidance and manufacturer’s declaration – Electromagnetic immunity
The REHAB SERIES device is intended for use in the electromagnetic environment specified
below. The customer or the user of the REHAB SERIES device should assure that it is used
in such an environment.
Immunity test
Electrostatic
discharge (ESD) to
IEC 61000-4-2
Electrical fast
transient / burst to
IEC 61000-4-4
Surge
IEC 6100-4-5
Voltage dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
± 6 kV contact
± 8 kV air
± 2 kV for
power supply lines
± 1 kV for
input /output lines
± 2 kV
for power supply lines
not applicable
± 1 kV
differential mode
± 2 kV
common mode
<5% UT
(>95% dip in UT for
0.5 cycle) 40% UT
(60% dip in UT for
5 cycles) 70% UT
(30% dip in UT for
25 cycles) <5% UT
(>95% dip in UT for
5 seconds)
<5% UT
(>95% dip in UT for
0.5 cycle) 40% UT
(60% dip in UT for 5
cycles) 70% UT
(30% dip in UT for 25
cycles) <5% UT
(>95% dip in UT for 5
seconds)
± 6 kV contact
± 8 kV air
IEC 60601
test level
Compliance
level
Electromagnetic
environment - Guidance
Power frequency
(50/60 Hz)
magnetic field to
IEC 61000-4-8
Note: UT is the AC mains voltage prior to application of the test level.
3 A/m
3 A/m
Power frequency magnetic
fields should be at levels
characteristic of a typical
location in a typical
commerical or hospital
environment.
Mains power quality should
be that of a typical
commercial or hospital
environment. If the use
of the REHAB SERIES
device requires continued
operation during mains
power interruptions,
it is recommended to
install a battery.
Mains power quality should
be that of a typical
commercial or hospital
environment.
Mains power quality should
be that of a typical
commercial or hospital
environment.
Floors should be wood,
concrete or ceramic tile.
If floors are covered with
synthetic material, the
relative humidity should
be at least 30%.
± 1 kV
differential mode
± 2 kV
common mode
83
Rehab-Series
