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.

Back to MHRA

Manufacturer's By Device SARS-CoV-2 immunoglobulin G (IgG)/IgM/neutralizing antibody IVD kit rapid ICT clinical-SARS-CoV-2 immunoglobulin G (IgG)/IgM/neutralizing antibody IVD kit rapid ICT clinical

Displaying 1 to 1 of 1

Page(s) 1

Manufacturer	Address	Authorised Representative	Address	Date Registered	MHRA Reference Number
Hoyotek Biomedical Co. Ltd.	Floor 4 Zone C Workshop No. 1 China Civil Aviation Science and Technology Industrialization Base No. 225 Jinger Road Tianjin Airport Economic Zone Tianjin 300308 China	QAdvis UK Ltd	55-66 Frederick Street Edinburgh EH2 1LS EH2 1LS Scotland United Kingdom	01/23/2023	23248

Manufacturer's By Device SARS-CoV-2 immunoglobulin G (IgG)/IgM/neutralizing antibody IVD kit rapid ICT clinical-SARS-CoV-2 immunoglobulin G (IgG)/IgM/neutralizing antibody IVD kit rapid ICT clinical

Contact details