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decreased immunity of the device.
4.6 Guidance and manufacturer’s declaration – electro-
magnetic immunity
These devices are intended for use in the electromagnetic environment
specified below. The customer or the user of the device should assure that
the device is used in such an environment.
Immunity
IEC
Compliance
Elec
tromagnetic
Test
60601-1-2
level
environment—
test level
guidance
Electro-
±6 kV
±6 kV
Floors should be wood,
static
contact
contact
concrete or ceramic tile.
discharge
±8 kV air
±8 kV air
If floors are covered
(ESD)
with synthetic material,
IEC
the relative humidity
61000-4-2
should be at least 30%.
Electrical
±2 kV
±2 kV
Mains power quality
fast
for power
for power
should be that of a
transient/
supply
supply
typical commercial or
burst
lines
lines
hospital environment.
IEC
±1 kV
±1 kV
61000-4-4
for input/
for input/
output
output
lines
lines
Surge
±1 kV
±1 kV
Mains power quality
IEC
line(s) to
line(s) to
should be that of a
61000-4-5
line(s)
line(s)
typical commercial or
±2 kV
±2 kV
hospital environment.
line(s) to
line(s) to
earth
earth
Voltage
<5% UT
<5% UT
Mains power quality
dips, short
(>95% dip
(>95% dip
should be that of a
interrup-
in UT)
in UT)
typical commercial or
tions and
for 0.5
for 0.5
hospital environment.
voltage
cycle
cycle
If the user of the device
variations
40% UT
40% UT
requires continued operation
Summary of Contents for ApneBoot
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