United Kingdom MHRA device registration 73566

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

United Kingdom flagUnited Kingdom·In Vitro Diagnostic Device·bioMérieux S.A·Registered Nov 26, 2024
Registration details
Device ID
73566
MHRA Reference Number
73566
Date Registered
Nov 26, 2024
Last Updated
May 17, 2024
Device classification
Device Type
In Vitro Diagnostic Device
Devices
Toxoplasma gondii immunoglobulin G (IgG) antibody avidity index IVD, kit, enzyme immunoassay (EIA)
Type
IVD Annex II List B
Manufacturer
Address
bioMérieux S.A
Marcy L'Etoile (69280), France
Created Date
Mar 30, 2021
Authorized Representative
Relationship Type
UK Responsible Person
Address
Chineham Gate Crockford Lane
Basingstoke, Hampshire, England, United Kingdom
Postcode: RG24 8NA
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About this record

Toxoplasma gondii immunoglobulin G (IgG) antibody avidity index IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 73566. 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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