Clinical specimen extraction buffer IVD - UK MHRA Medical Device Registration
Clinical specimen extraction buffer IVD is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 150419. The device is manufactured by Eurospital S.p.A. from Italy, 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
Clinical specimen extraction buffer IVD
Type
Class A
Date Registered
Nov 26, 2024
Last Updated
Oct 23, 2024
Address
Via Flavia 122
TRIESTE, Friuli-Venezia Giulia, Italy
Created Date
May 20, 2021
Name
Qarad UK Ltd.Relationship Type
Address
8 Northumberland Ave
Westminster, London , England, United Kingdom
Postcode: WC2N 5BY
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