Compliance Information - Sonova Phonak Audeo L-312 User Manual

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19. Compliance information

Europe:
Declaration of Conformity for the hearing aid
Hereby Sonova AG declares that this product meets the
requirements of the Medical Devices Regulation (EU)
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 www.phonak.com/en-int/certificates
(Phonak worldwide locations).
Australia/New Zealand:
44
PH_UserGuide_Audeo_L-312_92x125_EN_V1.00_029-1326-02.indd 44
PH_UserGuide_Audeo_L-312_92x125_EN_V1.00_029-1326-02.indd 44
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.
2023-12-04 11:42:47 AM
2023-12-04 11:42:47 AM

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Phonak audeo l-312 trialPhonak audeo l90-312Phonak audeo l70-312Phonak audeo l50-312Phonak audeo l30-312

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