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The device is designed to operate in the electromagnetic environment specified
below. The customer or the user must guarantee that it is used in this environment.
Immunity test
Level
indicated
by EN
60601-1-2
ESD
± 6kV
(EN 61000-4-2)
contact;
±8kV in air
Fast Transient
± 2kV for
Burst
power supply
(EN61000-4-4)
and ; ±1kV
for the signal
conductors
Over voltage
± 1kV
(EN 61000-4-5)
differential
mode; ± 2kV
common
mode
Voltage dips,
<5% Ut
brief voltage
(>95% dip in
Interruptions
Uv)
and variations
For 0,5
on the power
cycles
supply line
40% Ut
(60% dip in
Uv)
For 5 cycles
70% Ut
(30% dip in
Uv)
For 25 cycles
<5% Ut
(>95% dip in
Uv)
For 5 sec
EN 61000-4-11
Network
3 A/m
frequency
magnetic field
(50/60Hz)
(EN 61000-4-8)
This device is designed to operate in the electromagnetic environment specified
below. The customer or the user must guarantee that it is used in this environment.
emc_cardioline
Conformit
Guide to the
y level
electromagnetic
environment
conforms
The floor must be of wood,
concrete or ceramic. If
covered with synthetic
material, the relative
humidity must be at least
30%
conforms
The power supply network
quality must be typical of a
commercial or hospital
environment
conforms
The power supply network
quality must be typical of a
commercial or hospital
environment
not
The device operates with
applicable
buffer batteries and is
designed for continuous
operation
conforms
Network frequency
magnetic field should have
levels typical of
installations in commercial
or hospital environments
Rel. 1.xx – Ed. 1.0
Immunity
®
CARDIOLINE
is an et medical devices SpA brand
w w w . c a r d i o l i n e . b i z
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