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

Back to MHRA

Manufacturer's Devices - Agendia N.V.

Address:

Radarweg 60

Amsterdam

1043 NT

Netherlands

Authorised Representative/ UK Responsible Person
Name: Qserve Group UK Ltd.
Address:

49 Greek Street

London

W1D 4EG

England United Kingdom

Code/Term Type

General specimen collection kit IVD clinical General specimen collection kit IVD clinical IVD General

General specimen collection kit IVD clinical General specimen collection kit IVD clinical Class A

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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Code/Term		Type
General specimen collection kit IVD clinical	General specimen collection kit IVD clinical	IVD General
General specimen collection kit IVD clinical	General specimen collection kit IVD clinical	Class A