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Sm/RNP antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Sm/RNP 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 203810. 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..

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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In Vitro Diagnostic Device
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Sm/RNP antibody IVD, kit, enzyme immunoassay (EIA)
MHRA Device ID: 203810โ€ขRef: 203810

Device Type

In Vitro Diagnostic Device

Devices

Sm/RNP antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 26, 2024

Manufacturer Information

Address

Via Giosuรจ Carducci, 27 20099 Sesto San Giovanni

Milan, Italy

Created Date

Oct 24, 2024

Authorized Representative

Relationship Type

UK Responsible Person

Address

405 Wharfedale Road

Wokingham, Berkshire, England, United Kingdom

Postcode: RG41 5RA

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