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 - Wuhan EasyDiagnosis Biomedicine Co. Ltd.

Address:

Room 3 & 4 2nd Floor Bldg 25 Phase 3.1 Wuhan Optics Valley International Biopharmaceutical Enterprise Accelerator No. 388 Gaoxin 2nd Road East Lake Hi-Tech Development Zone

Wuhan

Hubei 430074

China

Authorised Representative/ UK Responsible Person
Name: Bioteck Limited
Address:

1 The Green

Richmond

TW9 1PL

England United Kingdom

Code/Term Type

SARS-CoV-2 antigen IVD kit rapid ICT self-testing SARS-CoV-2 antigen IVD kit rapid ICT self-testing IVD Devices for Self-Testing

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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