Hepatitis A virus total antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Hepatitis A virus total 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 121751. The device is manufactured by DiaSorin Italia S.p.A. from Italy, classified as In Vitro Diagnostic Device. The authorized representative in the UK is DiaSorin Italia S.p.A. UK Branch.

This page provides comprehensive regulatory information including complete registration details, manufacturer information, device classification, authorized representative details, and related products. Pure Global AI offers free access to 150,962+ UK MHRA medical device registrations, helping global MedTech companies identify partners, analyze markets, and discover business opportunities efficiently.

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Hepatitis A virus total antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 121751•Ref: 121751

Device Type

In Vitro Diagnostic Device

Devices

Hepatitis A virus total antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Sep 24, 2024

Last Updated

Jun 7, 2024

Manufacturer Information

Name

DiaSorin Italia S.p.A.

Address

DiaSorin Italia S.p.A. Via Crescentino SALUGGIA

VC, Piemonte, Italy

Created Date

Apr 27, 2021

Authorized Representative

Name

DiaSorin Italia S.p.A. UK Branch

Relationship Type

UK Responsible Person

Address

Central Road

Dartford, England, United Kingdom

Postcode: DA1 5LR

DJ Fang

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Hepatitis A virus total antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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DJ Fang

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