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 Bordetella pertussis immunoglobulin G (IgG) antibody IVD kit enzyme immunoassay (EIA)-Bordetella pertussis immunoglobulin G (IgG) antibody IVD kit enzyme immunoassay (EIA)
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
NeoMedica doo
Bulevar Svetog Cara Konstantina 82-86
Nis
18103
Serbia
Wellkang Ltd
Enterprise Hub NW Business Complex 1 Beraghmore Road
Derry Northern Ireland
BT48 8SE
Northern Ireland United Kingdom
11/26/2020
11006
Virion\Serion GmbH
Friedrich-Bergius-Ring 19
Wurzburg
97076
Germany
Launch Diagnostics Limited
Ash House Ash Road New Ash Green
Longfield
Kent DA3 8JD
United Kingdom
07/21/2021
16021