Guidance and manufacturer’s declaration
–
electromagnetic emission
Emission test
RF emissions
GB4824
Group 1
RF emissions
GB4824
Harmonic emissions
GB17625.1
Voltage fluctuations/
flicker emissions
GB17625.2
Group B
Class A
Compliant
Compliance
Electromagnetic environment
–
guidance
22
23
The instrument conforms to the requirements of electromagnetic compatibility of GB9706.1：
2007/YY0505-2012. The instrument doesn't require any installation. Please use and operate this
instrument according to the Guidance and Manufacturer's Declaration in below table.
The BreathCare PAP device is intended for use in the electromagnetic environment specified below. The
customer or the user of the PAP device should assure the instrument is used in such an environment.
The the BreathCare PAP device uses RF energy only for
its internal function. Therefore, its RF emissions are
very low and are not likely to cause any interference in
nearby electronic equipment.
The BreathCare PAP device is suitable for use in all
establishments, including domestic establishments
and those directly connected to the public
low-voltage power supply network that supplies
buildings used for domestic purposes.
Guidance and manufacturer's declaration
–
electromagnetic emissions
–
for all EQUIPMENT and SYSTEMS
Guidance and manufacturer's declaration
–
electromagnetic immunity
–
for all EQUIPMENT and SYSTEMS
Guidance and manufacturer's declaration
–
electromagnetic immunity
Immunity test
Electrostatic
discharge (ESD)
GB/T17626.2
±6 kV contact
±8 kV air
±6 kV contact
±8 kV air
<5% U
T
, (>95% dip
in U
T
) for 0.5 cycle
40% U
T
, (60% dip
in U
T
) for 5 cycle
70% U
T
,(30% dip
in U
T
) for 25 cycle
<5% U
T
,(>95% dip
in U
T
) for 5 seconds
<5% U
T
, (>95% dip
in U
T
) for 0.5 cycle
40% U
T
, (60% dip
in U
T
) for 5 cycle
70% U
T
,(30% dip
in U
T
) for 25 cycle
<5% U
T
,(>95% dip
in U
T
) for 5 seconds
Electrical fast
transient/burst
GB/T17626.4
Surge
GB/T17626.5
Voltage dips,
short
interruptions
and voltage
variations on
power supply
input lines
GB/T17626.11
±2 kV to power
supply lines
±1 kV to input/
output lines
±1 kV lines to lines
±2 kV lines to ground
±1 kV lines to lines
±2 kV lines to ground
±2 kV to power
supply lines
Not applicable
IEC 60601 test level
Compliance level
Electromagnetic environment - guidance
The BreathCare PAP decice is intended for use in the electromagnetic environment specified
below. The customer or the user of the PAP device should assure the instrument is used in such
an environment.
Floors should be wood, concrete or
ceramic tile. If floor 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
BreathCare PAP device requires
continued operation during power
mains interruptions, it is recommended
that the BreathCare PAP device be
powered from an uninterruptible power
supply.
