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

Coxiella burnetii 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 74270. 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 Launch Diagnostics Limited.

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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Coxiella burnetii immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 74270•Ref: 74270

Device Type

In Vitro Diagnostic Device

Devices

Coxiella burnetii immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Oct 27, 2024

Last Updated

Apr 5, 2024

Manufacturer Information

Name

Dia.Pro Diagnostic Bioprobes S.r.l.

Address

27 Via Giosue Carducci SESTO SAN GIOVANNI

MI, Lombardia, Italy

Created Date

Apr 20, 2021

Authorized Representative

Name

Launch Diagnostics Limited

Relationship Type

UK Responsible Person

Address

Unit 20 Ash Way Thorp Arch Estate

Wetherby, England, United Kingdom

Postcode: LS23 7FA

DJ Fang

MedTech Regulatory Expert

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

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