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 - Biogroup laboratory limited

Address:

21 evesham street The studio building

London

London

W11 4AJ

England United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Home blood collection kit IVD Home blood collection kit IVD IVD General

Oral/upper respiratory tract specimen collection kit IVD home-use Oral/upper respiratory tract specimen collection kit IVD home-use IVD General

Faecal specimen collection kit IVD home-use Faecal specimen collection kit IVD home-use IVD General

General specimen collection kit IVD home-use General specimen collection kit IVD home-use 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
Home blood collection kit IVD	Home blood collection kit IVD	IVD General
Oral/upper respiratory tract specimen collection kit IVD home-use	Oral/upper respiratory tract specimen collection kit IVD home-use	IVD General
Faecal specimen collection kit IVD home-use	Faecal specimen collection kit IVD home-use	IVD General
General specimen collection kit IVD home-use	General specimen collection kit IVD home-use	IVD General