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 - Audio Technologies Srl

Address:

Via Dell'Artigianato 8

GOSSOLENGO

PC

Emilia-Romagna 29020

Italy

Authorised Representative/ UK Responsible Person
Name: Delta Surgical Limited
Address:

Unit 10 Evolution Lymedale Business Park

Newcastle under Lyme

Staffordshire ST5 9QF

United Kingdom

Code/Term Type

Dura mater biomatrix implant Dura mater biomatrix implant Class III

Ossicular prosthesis partial Ossicular prosthesis partial Class IIb

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
Dura mater biomatrix implant	Dura mater biomatrix implant	Class III
Ossicular prosthesis partial	Ossicular prosthesis partial	Class IIb