Hepatitis E virus total antibody IVD, kit, chemiluminescent immunoassay - UK MHRA Medical Device Registration

Hepatitis E virus total antibody IVD, kit, chemiluminescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 203831. The device is manufactured by DIA.PRO Diagnostic Bioprobes S.r.l. from Italy, classified as In Vitro Diagnostic Device. The authorized representative in the UK is A. Menarini Diagnostics Ltd..

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In Vitro Diagnostic Device

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Hepatitis E virus total antibody IVD, kit, chemiluminescent immunoassay

MHRA Device ID: 203831•Ref: 203831

Device Type

In Vitro Diagnostic Device

Devices

Hepatitis E virus total antibody IVD, kit, chemiluminescent immunoassay

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 26, 2024

Manufacturer Information

Name

DIA.PRO Diagnostic Bioprobes S.r.l.

Address

Via Giosuè Carducci, 27 20099 Sesto San Giovanni

Milan, Italy

Created Date

Oct 24, 2024

Authorized Representative

Name

A. Menarini Diagnostics Ltd.

Relationship Type

UK Responsible Person

Address

405 Wharfedale Road

Wokingham, Berkshire, England, United Kingdom

Postcode: RG41 5RA

DJ Fang

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Hepatitis E virus total antibody IVD, kit, chemiluminescent immunoassay - UK MHRA Medical Device Registration

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Created Date

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DJ Fang

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