Multiple traumatic brain injury marker IVD, kit, enzyme immunoassay (EIA), rapid - UK MHRA Medical Device Registration
Multiple traumatic brain injury marker IVD, kit, enzyme immunoassay (EIA), rapid is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 134468. The device is manufactured by Abbott Point of Care 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
Multiple traumatic brain injury marker IVD, kit, enzyme immunoassay (EIA), rapid
Type
IVD General
Date Registered
Jan 28, 2022
Last Updated
Jan 24, 2023
Address
400 College Road East
Princeton, New Jersey, United States
Created Date
Jan 28, 2022
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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