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

Rubella virus immunoglobulin M (IgM) antibody IVD, kit, chemiluminescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 193506. 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.

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

MHRA Device ID: 193506•Ref: 193506

Device Type

In Vitro Diagnostic Device

Devices

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

Type

Class C

Date Registered

Nov 26, 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

MedTech Regulatory Expert

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

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