Estradiol (oestradiol) (E2) IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Estradiol (oestradiol) (E2) IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 202181. 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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Estradiol (oestradiol) (E2) IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 202181•Ref: 202181

Device Type

In Vitro Diagnostic Device

Devices

Estradiol (oestradiol) (E2) 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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Estradiol (oestradiol) (E2) IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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