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 - European Orthopaedic Centre

Address:

M. Birli - A. Tsitouras O.E. Aigaiou 12 Str.

Near Smyrni

South Athens

Attica 171 21

Greece

Authorised Representative/ UK Responsible Person
Name: Portsand Ltd T/A Brace Orthopaedic
Address:

Unit 8 Evans Business Centre Orion Business Park

Orion Way North Shields

North Shields

Tyne & Wear NE29 7SN

England United Kingdom

Code/Term Type

Ankle/foot orthosis Ankle/foot orthosis 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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