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 Enterovirus immunoglobulin M (IgM) antibody (serotypes 68-71) IVD reagent-Enterovirus immunoglobulin M (IgM) antibody (serotypes 68-71) IVD reagent
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Manufacturer
Address
Authorised Representative
Address
Date Registered
MHRA Reference Number
CITEST DIAGNOSTICS INC
170-422 Richards Street Vancouver BC
V6B 2Z4 Canada
Vancouver
V6B 2Z4
Canada
UK RepMed Ltd.
Wey Court West Union Road
Farnham Surrey
Farnham
GU9 7PT
England United Kingdom
08/11/2021
16644
Guangzhou Wondfo Biotech Co. Ltd.
No.8 Lizhishan Road Science City Luogang District
Guangzhou
510663
China
Qarad UK Ltd.
8 Northumberland Ave
Westminster
London WC2N 5BY
England United Kingdom
03/07/2021
12536