SARS-CoV-2 immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

SARS-CoV-2 immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 96218. The device is manufactured by Aikang Diagnostics Co Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Medimap Ltd.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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

MHRA Device ID: 96218

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD General

Date Registered

Jul 22, 2021

Last Updated

Dec 22, 2022

Manufacturer Information

Name

Aikang Diagnostics Co Ltd.

Address

501 Building 1&3 Hongxin Industrial Park Guanguang Road 1303 Guanlan Longhua District

Guangdong, Shenzhen, China

Created Date

Jul 22, 2021

Authorized Representative

Name

Medimap Ltd

Relationship Type

UK Responsible Person

Address

2 The Drift

Thurston, Suffolk, United Kingdom

Postcode: IP31 3RT

DJ Fang

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Other Products from Aikang Diagnostics Co Ltd. (2)

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

Type: In Vitro Diagnostic Device

Registered: Jul 22, 2021

SARS-CoV-2 neutralizing antibody IVD, kit, enzyme immunoassay (EIA)

Type: In Vitro Diagnostic Device

Registered: Jul 22, 2021

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SARS-CoV-2 immunoglobulin G (IgG)/IgM antibody IVD, kit, rapid ICT, clinical - UK MHRA Medical Device Registration

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