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 Gliadin antibody IVD kit fluorescent immunoassay-Gliadin antibody IVD kit fluorescent immunoassay
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
EUROIMMUN Medizinische Labordiagnostika AG
Seekamp 31
Lubeck
23560
Germany
Euroimmun UK Limited
Ashville House 131-139 The Broadway
Wimbledon
London SW19 1QJ
England United Kingdom
05/05/2021
14448
Phadia AB
Rapsagatan 7P PO. Box 6460
751 37 Uppsala
Uppsala
Uppsala Län 751 37
Sweden
Thermo Fisher Diagnostics Ltd.
16 Shenley Pavillions Chalkdell Drive
Shenley Wood
Milton Keynes
MK5 6LB
England United Kingdom
04/06/2023
23998