Pure Global

Multiple autoimmune disease-associated antibody screening IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration

Multiple autoimmune disease-associated antibody screening IVD, kit, fluorescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 149673. The device is manufactured by A. Menarini Diagnostics 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.

Free Database
Powered by Pure Global AI
MHRA Registered
In Vitro Diagnostic Device
๐Ÿ‡ฌ๐Ÿ‡ง
Multiple autoimmune disease-associated antibody screening IVD, kit, fluorescent immunoassay
MHRA Device ID: 149673โ€ขRef: 149673

Device Type

In Vitro Diagnostic Device

Devices

Multiple autoimmune disease-associated antibody screening IVD, kit, fluorescent immunoassay

Type

IVD General

Date Registered

Aug 18, 2024

Last Updated

Feb 29, 2024

Manufacturer Information

Address

Via Sette Santi 3

Florence, Italy

Created Date

Aug 16, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

405 Wharfedale Road

Wokingham, Berkshire, England, United Kingdom

Postcode: RG41 5RA

Pure Global
DJ Fang

DJ Fang

MedTech Regulatory Expert

Need help with 30+ markets registration?

Pricing