Electromagnetic Immunity - ARTROMOT SP3 Instrucciones De Uso

12.2 Electromagnetic immunity

Guidance and Manufacturer's Declaration – Electromagnetic Immunity
ARTROMOT®-SP3 is intended for use in the electromagnetic environment specified below.
It is the responsibility of the customer or user to ensure that the ARTROMOT®-SP3 unit is
used in such an environment.
Immunity test IEC 60601
test level
Home healthcare
Electrostatic ± 8 kV contact
discharge (ESD) to
± 15 kV air
IEC 61 000-4-2
Electrical fast
± 2 kV
transient/bursts to 100 kHz repetition
IEC 61 000-4-4 frequency
Surges to ± 1 kV
IEC 61 000-4-5 line-to-line
voltage
Voltage dips 0% U
To IEC 61000-4-11 at
0°, 45°, 90°, 135°,
180°, 225°, 270°,
315°
0% U
and
70% U
cycles
Single phase at 0°
Voltage 0% U
interuptions to cycles
IEC 61000-4-11
Power frequency 30 A/m
(50/60 Hz)
magnetic field to
IEC 61 000-4-8
Note: U
is the a.c. mains voltage prior to application of the test level.
t
Compliance
level
Home healthcare
± 8 kV contact
± 15 kV air
± 2 kV
100 kHz repetition
frequency
± 1 kV
line-to-line
voltage
; 0,5 cycle 0% U ; 0,5 cycle
t t
at
0°, 45°, 90°, 135°,
180°, 225°, 270°,
315°
; 1 cycle 0% U ; 1 cycle
t t
and
; 25/30 70% U
t t
cycles
Single phase at 0°
; 250/300 0% U ; 250/300
t t
cycles
30 A/m
227
Electromagnetic
environment – guidance
Floors should be wood, con-
crete or ceramic tile. If floors
are covered with synthetic
material, the relative humidity
should be at least 30%.
Mains power should be that
of a typical commercial or
hospital environment.
Mains power should be that
of a typical commercial or
hospital environment.
Mains power should be that
of a typical commercial or
hospital environment. If the
user of the ARTROMOT®-SP3
unit requires continued
operation during power mains
interruptions, it is recommen-
ded that the ARTROMOT®-SP3
; 25/30
unit be powered from an
uninterruptible power supply
or a battery.
Power frequency magnetic
fields should be at levels
characteristics of a typical
location in a typical commer-
cial or hospital environment.