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 - Amplifon SpA

Address:

Via Giuseppe Ripamonti 131/133

Milano

20141

Italy

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

Amplifon Ltd Gateway House

Styal Road Manchester

Manchester

Greater Manchester M22 5WY

England United Kingdom

Code/Term Type

Audiometric/hearing device software Audiometric/hearing device software 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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