Electromagnetic Compatibility; Guidance And Manufacturer's Declaration; Din En 60601-1-2:2007; Electromagnetic Emissions - INQUA Inhalator Instrucciones De Uso

Electromagnetic compatibility -

Guidance and manufacturer's declaration

Equipment Under Test (EUT): INQUA
Medical electrical devices are subject to special precautionary measures in particular
regarding the EMV with the installation and the operation.
Portable and mobile HF-communication devices e.g. mobile phone can affect medical
electrical devices.
A use of other accessories and lines than the indicated, can lead to an increased sending
or a reduced noise immunity of the equipment. The equipment has to be operated exclu-
sively with original accessories.
The device should not be used adjacent to or stacked with other equipment. If adjacent or
stacked use is necessary, the device should be observed to verify normal operation in the
configuration in which it will be used.
The EUT is intended for use in the electromagnetic environment specified below. The
customer or the user of the EUT should assure that it is used in such environment.

ELECTROMAGNETIC EMISSIONS

Emission test
RF emissions
CISPR 11
Harmonic emissions
IEC 61000-3-2
Voltage fluctuations /
flicker emissions
IEC 61000-3-3

DIN EN 60601-1-2:2007

(IEC 60601-1-2:2007)
Compliance Electromagnetic environment – Guidance
Group 1
Class B
Class A
Passed
®
Inhalator
EUT uses RF energy only for its internal func-
tion.
Therefore, RF-emission is very low and are not
likely to cause any interference in nearby elec-
tronic equipment.
The EUT is suitable for use in all establish-
ments, including domestic establishments and
those directly connected to the public low-volt-
age power supply network that supplies build-
ings used for domestic purposes.
Table 1 of DIN EN 60601-1-2:2007 (IEC 60601-1-2:2007)
181