SPORT-ELEC FARMADOLOR Manual De Uso página 27

GUIDANCE AND MANUFACTURER'S DECLARATION
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
Electrostatic
discharge
(ESD)
IEC 61000-4-2
Electrical fast
±2 kV for power supply lines
transient/burst
IEC 61000-4-4
±1 kV line(s) and neutral
Surge
IEC 61000-4-5
± 2 kV line(s) to earth
Voltage <5 % U
dips, short
interruptions
40 % U
and voltage
variations
70 % U
on power supply
input lines
<5 % U
IEC 61000-4-11
Power frequency
(50/60 Hz)
magnetic field
IEC 61000-4-8
NOTE - U is the a.c. mains voltage prior to application of the test level
T
ELECTROMAGNETIC IMMUNITY
COMPLIANCE
±6 kV contact
±6 kV contact
±8 kV air
Not applicable
and dc lines
Not applicable
(>95 % dip in U )
T T
for 0,5 cycle
(60 % dip in U )
T T
for 5 cycles
Not applicable
(30 % dip in U )
T T
for 25 cycles
(>95 % dip in U )
T T
for 5s
3 A/m
ELECTROMAGNETIC
LEVEL ENVIRONMENT - GUIDANCE
Floors should be wood, concrete
or ceramic tile. If floors are
covered with synthetic material,
±8 kV air
the relative humidity should be at
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.
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
Power frequency magnetic
fields should be at levels
3A/m characteristic of a typical location
in a typical commercial or hospital
environment.
least 30 %.
a battery.