United Kingdom MHRA device registration 129385

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

United Kingdom·In Vitro Diagnostic Device·Bio-Rad ·Registered Nov 26, 2024

Registration details

Device ID: 129385
MHRA Reference Number: 129385
Date Registered: Nov 26, 2024
Last Updated: Apr 16, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Rubella virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Type: IVD Annex II List B

Manufacturer

Name: Bio-Rad
Address: 3, boulevard Raymond Poincaré
Marnes-la-Coquette, France
Created Date: Dec 29, 2021

Authorized Representative

Name: BIO-RAD LABORATORIES LIMITED
Relationship Type: UK Responsible Person
Address: The Junction 3rd And 4th Floor, Station Road, Watford, United Kingdom, WD17 1ET
WATFORD, Hertfordshire, England, United Kingdom
Postcode: wd17 1et

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About this record

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 129385. The device is manufactured by Bio-Rad from France, classified as In Vitro Diagnostic Device. The authorized representative in the UK is BIO-RAD LABORATORIES LIMITED.

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