Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Toxoplasma gondii 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 73644. The device is manufactured by bioMérieux S.A from France, classified as In Vitro Diagnostic Device. The authorized representative in the UK is bioMérieux 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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In Vitro Diagnostic Device

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Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 73644•Ref: 73644

Device Type

In Vitro Diagnostic Device

Devices

Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD Annex II List B

Date Registered

Nov 26, 2024

Last Updated

May 17, 2024

Manufacturer Information

Name

bioMérieux S.A

Address

bioMérieux S.A

Marcy L'Etoile (69280), France

Created Date

Mar 30, 2021

Authorized Representative

Name

bioMérieux UK Ltd

Relationship Type

UK Responsible Person

Address

Chineham Gate Crockford Lane

Basingstoke, Hampshire, England, United Kingdom

Postcode: RG24 8NA

DJ Fang

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Toxoplasma gondii immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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