7. Compliance information
Europe:
Declaration of Conformity
Hereby Sonova AG declares that this product meets the
requirements of the Medical Device Regulation 2017/745
as well as the Radio Equipment Directive 2014/53/EU. The
full text of the EU Declaration of Conformity can be
obtained from the manufacturer or the local Phonak
representative whose address can be taken from the list
on https://www.phonak.com/com/en/certificates.html
(Phonak worldwide locations).
Australia/New Zealand:
Indicates a device's compliance with applicable
Radio Spectrum Management's (RSM) and
Australian Communications and Media Authority
(ACMA) regulatory arrangements for the legal sale
in New Zealand and Australia.
The compliance label R-NZ is for radio products
supplied in the New Zealand market under
conformity level A1.
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FCC ID: KWCRX23
IC:
2262A-RX23
R 202-SMI050
In compliance with Regulation (EU) 2017/1354,
authorization for frequency use requirements in the
countries as shown on the pictogram below:
BE
DK
FR
IE
Notice 1:
This device complies with Part 15 of the FCC
Rules and with RSS-210 of Industry Canada.
Operation is subject to the following two
conditions:
1) this device may not cause interference, and
2) this device must accept any interference,
including interference that may cause undesired
operation of the device.
LT
MT
PT
SK
SI
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