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

Rubella virus immunoglobulin M (IgM) 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 180139. 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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In Vitro Diagnostic Device

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Rubella virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 180139•Ref: 180139

Device Type

In Vitro Diagnostic Device

Devices

Rubella virus immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)

Type

Class C

Date Registered

Nov 26, 2024

Last Updated

Apr 16, 2024

Manufacturer Information

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

DJ Fang

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

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