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

Hepatitis C 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 72948. The device is manufactured by Fujirebio Europe N.V. from Belgium, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK Ltd..

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In Vitro Diagnostic Device

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

MHRA Device ID: 72948•Ref: 72948

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD Annex II List A

Date Registered

Nov 26, 2024

Last Updated

May 9, 2024

Manufacturer Information

Name

Fujirebio Europe N.V.

Address

Technologiepark 6

Gent, Oost-Vlaanderen, Belgium

Created Date

Apr 13, 2021

Authorized Representative

Name

Qarad UK Ltd.

Relationship Type

UK Responsible Person

Address

8 Northumberland Ave

Westminster, London , England, United Kingdom

Postcode: WC2N 5BY

DJ Fang

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

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