United Kingdom MHRA device registration 202203

Total estrogen (oestrogen) IVD, kit, enzyme immunoassay (EIA)

United Kingdom·In Vitro Diagnostic Device·Diagnostics Biochem Canada, Inc.·Registered Nov 26, 2024

Registration details

Device ID: 202203
MHRA Reference Number: 202203
Date Registered: Nov 26, 2024
Last Updated: Oct 4, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Total estrogen (oestrogen) IVD, kit, enzyme immunoassay (EIA)
Type: IVD General

Manufacturer

Name: Diagnostics Biochem Canada, Inc.
Address: 384 Neptune Crescent
London, Ontario , Canada
Created Date: Oct 1, 2024

Authorized Representative

Name: MedEnvoy UK Limited
Relationship Type: UK Responsible Person
Address: 85 Great Portland Street First Floor
London, England, United Kingdom
Postcode: W1W 7LT

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About this record

Total estrogen (oestrogen) IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 202203. 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.

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