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 HIV1/HIV2 antigen IVD kit enzyme immunoassay (EIA)-HIV1/HIV2 antigen IVD kit enzyme immunoassay (EIA)
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
Fujirebio Europe N.V.
Technologiepark 6
Gent
Oost-Vlaanderen 9052
Belgium
Qarad UK Ltd.
8 Northumberland Ave
Westminster
London WC2N 5BY
England United Kingdom
04/13/2021
13308