Gamma-hydroxybutyrate (GHB) IVD, reagent - UK MHRA Medical Device Registration
Gamma-hydroxybutyrate (GHB) IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 154061. The device is manufactured by CITEST DIAGNOSTICS INC from Canada, classified as In Vitro Diagnostic Device. The authorized representative in the UK is UK RepMed 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
Gamma-hydroxybutyrate (GHB) IVD, reagent
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
May 14, 2024
Address
170-422 Richards Street Vancouver BC V6B 2Z4 Canada
Vancouver, Canada
Created Date
Aug 3, 2021
Name
UK RepMed Ltd.Relationship Type
Address
Unit D, Crondall Place Coxbridge Business Park Alton Road Farnham, Surrey,
Farnham, England, United Kingdom
Postcode: GU10 5EH
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