35
At the end of the service life, replacement is recommended to ensure problem-free operation. In the
event of visible damage or a noticeably longer nebulisation time with the same substance and same
quantity of medication, the components must be replaced immediately.
11.6
Electromagnetic Compatibility (EMC)
CAUTION:
Guidance and Manufacturer’s Declaration
Electromagnetic Immunity Enclosure Port
The AKITA JET nebuliser is intended for use in the electromagnetic environment specified below. The
customer or the user of the AKITA JET nebuliser should assure that it is used in such an environment.
Immunity test
IEC 60601-1-2:2014
Test Condition
Compliance
Level
Electromagnetic Environment -
Guidance
Electrostatic
discharge (ESD)
IEC 61000-4-2
± 8 kV contact
± 8 kV contact
Floors should be wood, concrete or
ceramic tile. If floors are covered with
synthetic material, the relative humidity
should be at least 30 %.
± 15 kV air
± 15 kV air
3 V/m
3 V/m
Guidance and Manufacturer’s Declaration
Electromagnetic Emission
The AKITA JET nebuliser is intended for use in the electromagnetic environment specified below. The
customer or the user of the AKITA JET should assure that it is used in such an environment.
Emissions Test
Compliance
Electromagnetic Environment - Guidance
RF emissions
CISPR 11
Group 1
The AKITA JET nebuliser 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.
RF emissions
CISPR 11
Class B
The AKITA JET nebuliser 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.
Harmonic emissions
IEC 61000-3-2
Class A
Voltage fluctuations /
flicker emissions IEC 61000-3-3
Complies
