21
Compliance with emission and immunity standards
Emission standards EN 60601–1-2
IEC 60601–1-2
EN 55011
CISPR11
CISPR25
EN 55025
Immunity standards EN 60601-1-2
IEC 60601-1-2
IEC 60601-1-11
EN 61000-4-2
IEC 61000-4-2
EN 61000-4-3
IEC 61000-4-3
EN 61000-4-4
IEC 61000-4-4
EN 61000-4-5
IEC 61000-4-5
EN 61000-4-6
IEC 61000-4-6
EN 61000-4-8
IEC 61000-4-8
EN 61000-4-11
IEC 61000-4-11
IEC 60601-1
ISO 7637-2
9. Information and explanation of
symbols
With the CE symbol, Sonova AG conrms that this
product meets the requirements of the Medical Devices
Regulation MDR 2017/745
Indicates the medical device manufacturer, as
dened in EU Medical Devices Regulation MDR
2017/745
Indicates the Authorized representative in the
European Community. The EC REP is also the importer
to the European Union
This symbol indicates that it is important for the user to
read and take into account the relevant information in
this user guide
This symbol indicates that it is important for the user to
pay attention to the relevant warning notices in this user
guide
Important information for handling and product safety
©
Copyright symbol
This symbol confers that the electromagnetic
interference from the device is under limits approved
by the US Federal Communications Commission
Indicates the manufacturer’s serial number so that a
specic medical device can be identied