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 - Thriva Limited

Address:

Thriva Limited Classic House 6th Floor

174-180 Old Street

London

London EC1V 9BP

England United Kingdom

Authorised Representative/ UK Responsible Person
Name: Not Available

Address:

Code/Term Type

Capillary blood collection kit home-use Capillary blood collection kit home-use IVD General

Patient general health self-management software Patient general health self-management software Class I

Phlebotomy kit Phlebotomy kit

Sexually transmitted infection (STI) testing specimen collection kit IVD home-use Sexually transmitted infection (STI) testing 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
Capillary blood collection kit home-use	Capillary blood collection kit home-use	IVD General
Patient general health self-management software	Patient general health self-management software	Class I
Phlebotomy kit	Phlebotomy kit
Sexually transmitted infection (STI) testing specimen collection kit IVD home-use	Sexually transmitted infection (STI) testing specimen collection kit IVD home-use	IVD General