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 - Shenzhen Lvshiyuan Biotechnology Co. Ltd.

Address:

D Building No.2 Industrial Avenue Buxin Village Buxin Community Dapeng Subdistrict Office Dapeng New District Shenzhen 518120 China

Shenzhen

518120

China

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

59 St. Martin's Lane

London

Middlesex WC2N 4JS

England United Kingdom

Code/Term Type

SARS-CoV-2 antigen IVD kit rapid ICT clinical SARS-CoV-2 antigen IVD kit rapid ICT clinical 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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