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 - APrevent Biotech GmbH

Address:

Im Letten 3a

Feldkirch

6800

Austria

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

Preformed vocal cord medialization implant Preformed vocal cord medialization implant Class IIb

ENT surgical procedure kit non-medicated reusable ENT surgical procedure kit non-medicated reusable Class I

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
Preformed vocal cord medialization implant	Preformed vocal cord medialization implant	Class IIb
ENT surgical procedure kit non-medicated reusable	ENT surgical procedure kit non-medicated reusable	Class I