Multiple antinuclear antibody (ANA) screening IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Multiple antinuclear antibody (ANA) screening IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 79521. The device is manufactured by EUROIMMUN Medizinische Labordiagnostika AG from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Euroimmun UK 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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Multiple antinuclear antibody (ANA) screening IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 79521•Ref: 79521

Device Type

In Vitro Diagnostic Device

Devices

Multiple antinuclear antibody (ANA) screening IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Aug 31, 2024

Manufacturer Information

Name

EUROIMMUN Medizinische Labordiagnostika AG

Address

Seekamp 31

Lubeck, Germany

Created Date

May 5, 2021

Authorized Representative

Name

Euroimmun UK Limited

Relationship Type

UK Responsible Person

Address

Ashville House 131-139 The Broadway

Wimbledon, London, England, United Kingdom

Postcode: SW19 1QJ

DJ Fang

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Multiple antinuclear antibody (ANA) screening IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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