Guidance And Manufacturer'sdeclaration Electromagnetic Emissions - Agu N7 Mode D'emploi

In order to regulate the requirements for EMC with the aim to prevent unsafe product situa-
tions, the EN60601–1–2 standard has been implemented. The nebulizer AGU N7 (MBPN002)
conforms to the EN60601–1–2:2007 standard for both immunity and emissions.
Nevertheless, DO NOT use the nebulizer close to the strong electrical or electromagnetic
fields. This may result in incorrect operation and create a potentially unsafe situation.
Guidance and manufacturer's declaration – of AGU N7 (MBPN002)
GUIDANCE AND MANUFACTURER'S
DECLARATION ELECTROMAGNETIC EMISSIONS
Mesh–nebulizer (membrane) AGU N7 is intended for use in the electromagnetic environ-
ment specified below.
The customer or the user of the Mesh–nebulizer (membrane) AGU N7 should assure that it
is used in such an environment.
Emission test
RF emissions
CISPR 11
RF emissions CISPR 11
Harmonic emissions
IEC 61000–3–2
Voltage fluctuations /
flicker emissions
IEC 61000–3–3
EN
Compliance Electromagnetic environment–guidance
Group 1
The Mesh–nebulizer (membrane) AGU N7
uses RF energy only for its internal func-
tion. The RF emissions are low and may not
cause interference the material surrounding
electronic
Class B
The Mesh–nebulizer (membrane) AGU N7
is suitable for the whole institution, including
Class A
domestic establishments and those
directly connected to public low–voltage
power supply that provides housing
Compliance
for domestic use
63