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 - Diagam SA

Address:

40 Rue Du Parc Industriel

Ghislenghien

7822

Belgium

Authorised Representative/ UK Responsible Person
Name: IVDeology UKRP Ltd
Address:

22-23 The Joiners Shop Historic Dockyard

Chatham

Rochester

Kent ME4 4TZ

England United Kingdom

Code/Term Type

Buffered sample diluent IVD Buffered sample diluent IVD IVD General

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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