Interferon gamma release IVD, reagent - UK MHRA Medical Device Registration
Interferon gamma release IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 135328. The device is manufactured by Biocare Medical, LLC from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Emergo Consulting (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.
Device Type
In Vitro Diagnostic Device
Devices
Interferon gamma release IVD, reagent
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Apr 17, 2024
Address
60 Berry Drive
Pacheco, California, United States
Created Date
Dec 30, 2021
Relationship Type
Address
Compass House, Vision Park Histon c/o Cr360 โ UL International
Cambridge, England, United Kingdom
Postcode: CB24 9BZ
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