Total estrogen (oestrogen) IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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.

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.

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

MHRA Device ID: 202203•Ref: 202203

Device Type

In Vitro Diagnostic Device

Devices

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

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Oct 4, 2024

Manufacturer Information

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

DJ Fang

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Total estrogen (oestrogen) IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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