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 - AlgOss Biotechnologies GmbH

Address:

Schumanngasse 15

Vienna

1180

Austria

Authorised Representative/ UK Responsible Person
Name: Qarad UK Ltd.
Address:

8 Northumberland Ave

Westminster

London WC2N 5BY

England United Kingdom

Code/Term Type

Dental bone matrix implant synthetic Dental bone matrix implant synthetic Class III

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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