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 Fibrin monomer IVD kit nephelometry/turbidimetry-Fibrin monomer IVD kit nephelometry/turbidimetry
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
Diagnostica Stago
3 Allée Thérésa
Asnières-sur-Seine
92600
France
Diagnostica Stago UK
2 Theale Lakes Business Park Moulden Way
Sulhamstead
Theale
RG7 4GB
England United Kingdom
06/14/2022
20960