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 Centromere antibody IVD kit fluorescent immunoassay-Centromere antibody IVD kit fluorescent immunoassay
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
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