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 antigen IVD kit rapid microfluidic immunoassay clinical-SARS-CoV-2 antigen IVD kit rapid microfluidic immunoassay clinical
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
LumiraDx UK Ltd.
Unit 1 Block 5 Dumyat Business Park
Bond Street
Alloa
FK102PB
United Kingdom
05/06/2020
9941