GUIDANCE AND MANUFACTURER’S DECLARATION
ELECTROMAGNETIC IMMUNITY
The FarmaDolor is intended for use in the electromagnetic environment specified below. The
customer or the user of the FarmaDolor should assure that it is used in such an environment.
IMMUNITY TEST
IEC 60601 TEST LEVEL
COMPLIANCE
LEVEL
ELECTROMAGNETIC
ENVIRONMENT - GUIDANCE
Electrostatic
discharge
(ESD)
IEC 61000-4-2
±6 kV contact
±8 kV air
±6 kV contact
±8 kV air
Floors should be wood, concrete
or ceramic tile. If floors are
covered with synthetic material,
the relative humidity should be at
least 30 %.
Electrical fast
transient/burst
IEC 61000-4-4
±2 kV for power supply lines
and dc lines
Not applicable
Mains power quality should be that
of a typical commercial or hospital
environment.
Surge
IEC 61000-4-5
±1 kV line(s) and neutral
± 2 kV line(s) to earth
Not applicable
Mains power quality should be that
of a typical commercial or hospital
environment.
Voltage
dips, short
interruptions
and voltage
variations
on power supply
input lines
IEC 61000-4-11
<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 5s
Not applicable
Mains power quality should be
that of a typical commercial or
hospital environment. If a dips or an
interruption of mains power occurs,
the current of the FarmaDolor
may be dropped off from normal
level, it may be necessary to use
uninterruptible power supply or
a battery.
Power frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
3 A/m
3A/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
