DJO ARTROMOT-K1 Standard Mode D'emploi page 207

. Electromagnetic immunity
Guidance and Manufacturer's Declaration Electromagnetic Immunity
ARTROMOT® K is intended for use in the electromagnetic environment specified below.
It is the responsibility of the customer or user to ensure that the ARTROMOT® K unit is
used in such an environment.
Immunity test IEC
test level
Home healthcare
Electrostatic ±
discharge ESD to
±
IEC
Electrical fast ±
transient/bursts to
IEC
frequency
Surges to ±
IEC line to line
voltage
±
line to ground
voltage
Voltage dips
To IEC at
and
Single phase at °
Power frequency
/ Hz
magnetic field to
IEC
Voltage
interuptions to cycles
IEC
Note: U is the a.c. mains voltage prior to application of the test level.
Compliance
level
Home healthcare
kV contact ±
kV air ±
kV ±
kHz repetition
frequency
kV ±
line to line
voltage
kV ±
line to ground
voltage
% U ; , cycle % U ; , cycle
at
°, °, °, °, °,
°, °, °,
°
% U ; cycle % U ;
and
% U ; % U ;
/ cycles /
Single phase at °
A/m
% U ; / % U ;
cycles
Electromagnetic
environment
kV contact Floors should be wood, con
crete or ceramic tile. If floors
kV air
are covered with synthetic
material, the relative humidity
should be at least
kV Mains power should be that
kHz repetition of a typical commercial or
hospital environment.
kV Mains power should be that
of a typical commercial or
hospital environment.
kV
Mains power should be that
of a typical commercial or
°, °, °, hospital environment. If the
user of the ARTROMOT® K
°, °, °,
° unit requires continued
operation during power
cycle
mains interruptions, it is
recommended that the
ARTROMOT® K unit
cycles
be powered from an
uninterruptible power
supply or a battery.
A/m Power frequency magnetic
fields should be at levels
characteristics of a typical
location in a typical commer
cial or hospital environment.
/
guidance
%.