Public Access Database for Medical Device Registration

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

Manufacturer's By Name

By Device

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Manufacturer's Devices - Beijing Zhongjian Antai Diagnostic Technology Co. Ltd

Address:

29 Qingfeng Road West Daxing Biological Medicine Base

Zhongguancun Science & Technology Park

Beijing

102629

China

Authorised Representative/ UK Responsible Person
Name: BHA-Medical Limited
Address:

New Broad Street House New Broad Street

London

London EC2M 1NH

England United Kingdom

Code/Term Type

Monkeypox virus immunoglobulin M (IgM) antibody IVD kit rapid ICT clinical Monkeypox virus immunoglobulin M (IgM) antibody IVD kit rapid ICT clinical IVD General

Contact details

Freedom of information

0203 080 7272 (manned 10:00-16:00 hours working days) device.registrations@mhra.gov.uk

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