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 - Jiangsu Swirl Medical Technology Co. LTD

Address:

2F Building 1 Electronic Industrial Park No.9 Xindong Road Economic and Technological Development Zone

Nantong

Jiangsu Province 226000

China

Authorised Representative/ UK Responsible Person
Name: MedPath Limited
Address:

27 Old Gloucester Street

London

WC1N 3AX

England United Kingdom

Code/Term Type

SARS-CoV-2 immunoglobulin G (IgG)/IgM antibody IVD kit rapid ICT clinical SARS-CoV-2 immunoglobulin G (IgG)/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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