Dehydroepiandrosterone (DHEA) IVD, reagent - UK MHRA Medical Device Registration
Dehydroepiandrosterone (DHEA) IVD, reagent is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 202178. The device is manufactured by Diagnostics Biochem Canada, Inc. from Canada, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MedEnvoy 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
Dehydroepiandrosterone (DHEA) IVD, reagent
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Oct 4, 2024
Address
384 Neptune Crescent
London, Ontario , Canada
Created Date
Oct 1, 2024
Relationship Type
Address
85 Great Portland Street First Floor
London, England, United Kingdom
Postcode: W1W 7LT
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