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 - Dewei Medical Equipment Co. Ltd

Address:

5th Floor No.4 Building Shiyou Industrial Park Jun'an Shunde

Foshan

Guangdong 528329

China

Authorised Representative/ UK Responsible Person
Name: CMC Medical Devices LTD
Address:

Office 32 19-21 Crawford Street

London

W1H 1PJ

United Kingdom

Code/Term Type

Viral transport medium IVD Viral transport medium IVD IVD General

Nucleic acid extraction/isolation kit IVD Nucleic acid extraction/isolation kit IVD IVD General

SARS-CoV-2 neutralizing antibody IVD kit rapid ICT clinical SARS-CoV-2 neutralizing antibody IVD kit rapid ICT clinical IVD General

Oral/upper respiratory tract specimen collection kit IVD clinical Oral/upper respiratory tract specimen collection kit IVD 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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Code/Term		Type
Viral transport medium IVD	Viral transport medium IVD	IVD General
Nucleic acid extraction/isolation kit IVD	Nucleic acid extraction/isolation kit IVD	IVD General
SARS-CoV-2 neutralizing antibody IVD kit rapid ICT clinical	SARS-CoV-2 neutralizing antibody IVD kit rapid ICT clinical	IVD General
Oral/upper respiratory tract specimen collection kit IVD clinical	Oral/upper respiratory tract specimen collection kit IVD clinical	IVD General