Public Access Database for Medical Device Registration

Registration does not represent any form of accreditation, certification or approval by the UK Competent Authority(MHRA)
Where a conformity assessment certificate is listed as expired, existing products already placed on the market prior to the expiry may not be affected by this expiry and can continue to be used. This expiry stops new products being placed on the market until there is a new certificate of conformity

Manufacturer's By Name

By Device

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Manufacturer's Devices - Phonak AG

Address:

Phonak AG Laubisruetistrasse 28

Staefa

Zurich 8712

Switzerland

Authorised Representative/ UK Responsible Person
Name: Sonova UK Limited
Address:

Sonova House Lakeside Drive

Centre Park Square

Warrington

WA1 1RX

England United Kingdom

Code/Term Type

Air-conduction hearing aid receiver-in-canal Air-conduction hearing aid receiver-in-canal Class IIa

Air-conduction hearing aid in-the-ear Air-conduction hearing aid in-the-ear Class IIa

Air-conduction hearing aid behind-the-ear Air-conduction hearing aid behind-the-ear Class IIa

Contralateral hearing unit Contralateral hearing unit Class IIa

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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Code/Term		Type
Air-conduction hearing aid receiver-in-canal	Air-conduction hearing aid receiver-in-canal	Class IIa
Air-conduction hearing aid in-the-ear	Air-conduction hearing aid in-the-ear	Class IIa
Air-conduction hearing aid behind-the-ear	Air-conduction hearing aid behind-the-ear	Class IIa
Contralateral hearing unit	Contralateral hearing unit	Class IIa