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.
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Manufacturer's By Device SARS-CoV-2 immunoglobulin G (IgG)/IgM antibody IVD kit rapid microfluidic immunoassay clinical-SARS-CoV-2 immunoglobulin G (IgG)/IgM antibody IVD kit rapid microfluidic immunoassay clinical
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
CITEST DIAGNOSTICS INC
170-422 Richards Street Vancouver BC
V6B 2Z4 Canada
Vancouver
V6B 2Z4
Canada
UK RepMed Ltd.
Wey Court West Union Road
Farnham Surrey
Farnham
GU9 7PT
England United Kingdom
08/11/2021
16644
LumiraDx UK Ltd.
Unit 1 Block 5 Dumyat Business Park
Bond Street
Alloa
FK102PB
United Kingdom
05/06/2020
9941