SARS-CoV-2 immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

SARS-CoV-2 immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 148039. The device is manufactured by Immundiagnostik AG from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qserve Group UK, 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) antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 148039•Ref: 148039

Device Type

In Vitro Diagnostic Device

Devices

SARS-CoV-2 immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 31, 2024

Manufacturer Information

Name

Immundiagnostik AG

Address

Stubenwald-Allee 8a

Bensheim, Germany

Created Date

May 23, 2022

Authorized Representative

Name

Qserve Group UK, Ltd.

Relationship Type

UK Responsible Person

Address

49 Greek Street

London, England, United Kingdom

Postcode: W1D 4EG

DJ Fang

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SARS-CoV-2 immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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