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 - Arthrogen GmbH

Address:

Burgstaller Strasse 6

Gmund

D-83703

Germany

Authorised Representative/ UK Responsible Person
Name: Patient Choice International Ltd
Address:

Suite G1 Hartsboune House Delta Gain. Carpenders Park.

Watford

WD19 5EF

England United Kingdom

Code/Term Type

Autologous conditioned serum set Autologous conditioned serum set 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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