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 - Medifa GmbH & Co. KG

Address:

Industriestrabe 5

Finnentrop

57413

Germany

Authorised Representative/ UK Responsible Person
Name: DP Medical Systems Limited
Address:

15a Oakcroft Road

Chessington

Surrey KT9 1RH

England United Kingdom

Code/Term Type

General examination/treatment chair electric General examination/treatment chair electric 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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