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 - Bsure Medical BV

Address:

Achillesstraat 85 Amsterdam

Amsterdam

Provincie Noord-Holland 1076 PX

Netherlands

Authorised Representative/ UK Responsible Person
Name: Fagron UK Ltd
Address:

Media Exchange 4b Coquet Street

Newcastle Upon Tyne

NE1 2QB

United Kingdom

Code/Term Type

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

Human genomic analysis interpretive software IVD Human genomic analysis interpretive software 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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Code/Term		Type
General specimen collection kit IVD clinical	General specimen collection kit IVD clinical	IVD General
Human genomic analysis interpretive software IVD	Human genomic analysis interpretive software IVD	IVD General