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 - Genbody Inc

Address:

3-18 Eopseong 2-gil

Seobuk-gu Cheonan-si

Chungcheongnam-do

312-800

South Korea

Authorised Representative/ UK Responsible Person
Name: Phil and Adams Limited
Address:

2 Mannin Way

Lancaster

LA1 3SU

United Kingdom

Code/Term Type

SARS-CoV-2 antigen IVD kit fluorescent immunoassay rapid SARS-CoV-2 antigen IVD kit fluorescent immunoassay rapid 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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