Antisera matrix (non-reactive) IVD, control - UK MHRA Medical Device Registration
Antisera matrix (non-reactive) IVD, control is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 195221. The device is manufactured by DIAGAST from France, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad UK 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.
Device Type
In Vitro Diagnostic Device
Devices
Antisera matrix (non-reactive) IVD, control
Type
Class D
Date Registered
Nov 26, 2024
Last Updated
May 9, 2024
Name
DIAGASTAddress
Eurasantรฉ parc, 251, Avenue Eugรจne Avinรฉe
Loos, Nord, France
Created Date
Apr 15, 2021
Name
Qarad UK Ltd.Relationship Type
Address
8 Northumberland Ave
Westminster, London , England, United Kingdom
Postcode: WC2N 5BY
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