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

Rubella virus 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 73546. 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.

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Rubella virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 73546•Ref: 73546

Device Type

In Vitro Diagnostic Device

Devices

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

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