Guidance and manufacturer's declaration – electromagnetic immunity
The Aeroneb Go nebulizer system is intended for use in the electromagnetic
environment specified below. The customer or the user of the Aeroneb Go
should assure that it is used in such an environment.
Immunity test
Electrostatic
discharge (ESD)
IEC 61000-4-2
Electrical fast
Transient/burst
IEC 61000-4-4
Surge
IEC 61000-4-5
Voltage
dips, short
interruptions and
voltage variations
on power supply
input lines
IEC 61000-4-11
IEC/EN 60601
Test level
±6 kV contact
±8 kV air
±2 kV for power
supply lines
±1 kV for input/
output lines
±1 kV differential
mode
±2 kV common
mode
<5 % Ut
(>95 % dip in Ut)
for 0.5 cycle
40 % Ut
(60 % dip in Ut)
for 5 cycles
70 % Ut
(30 % dip in Ut)
for 25 cycles
<5 % Ut
(>95 % dip in Ut)
for 5 sec
Compliance
level
±6 kV contact
±8 kV air
±2 kV for power
supply lines
±1 kV for input/
output lines
±1 kV differential
mode
±2 kV common
mode
<5 % Ut
(>95 % dip in Ut)
for 0.5 cycle
40 % Ut
(60 % dip in Ut)
for 5 cycles
70 % Ut
(30 % dip in Ut)
for 25 cycles
<5 % Ut
(>95 % dip in Ut)
for 5 sec
Electromagnetic
environment –
guidance
Floors should be
wood, concrete or
ceramic tile. If floors
are covered with
synthetic material,
the relative humidity
should be at
least 30%.
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 the user of
the Aeroneb Go
requires continued
operation during
power mains
interruption, it is
recommended that
the Aeroneb Go
be powered from
an uninterruptible
power supply or
battery.