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 - JINAN BABIO BIOTECHNOLOGY CO. LTD.

Address:

303 Building 5 of SME Industrialization Base of Biomedical Park 1777 Dazheng Road High-tech Zone Jinan City 250101 Shandong Province China

Jinan

Shandong 250101

China

Authorised Representative/ UK Responsible Person
Name: PureUKCA Ltd
Address:

59 St. Martin's Lane

London

Middlesex WC2N 4JS

England United Kingdom

Code/Term Type

Oral/upper respiratory tract specimen collection swab IVD Oral/upper respiratory tract specimen collection swab IVD IVD General

General specimen collection kit IVD clinical General specimen collection kit IVD clinical IVD General

Monkeypox virus nucleic acid IVD kit nucleic acid technique (NAT) Monkeypox virus nucleic acid IVD kit nucleic acid technique (NAT) 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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Code/Term		Type
Oral/upper respiratory tract specimen collection swab IVD	Oral/upper respiratory tract specimen collection swab IVD	IVD General
General specimen collection kit IVD clinical	General specimen collection kit IVD clinical	IVD General
Monkeypox virus nucleic acid IVD kit nucleic acid technique (NAT)	Monkeypox virus nucleic acid IVD kit nucleic acid technique (NAT)	IVD General