Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 194606. The device is manufactured by HYCOR Biomedical Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Advena Ltd.

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Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, enzyme immunoassay (EIA)

MHRA Device ID: 194606•Ref: 194606

Device Type

In Vitro Diagnostic Device

Devices

Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, enzyme immunoassay (EIA)

Type

IVD General

Date Registered

Nov 26, 2024

Last Updated

Jun 5, 2024

Manufacturer Information

Name

HYCOR Biomedical Inc.

Address

7272 Chapman Avenue CA 92841 U.S.A.

Garden Grove, CA, United States

Created Date

May 30, 2024

Authorized Representative

Name

Advena Ltd

Relationship Type

UK Responsible Person

Address

Pure Offices Plato Close

Warwick, England, United Kingdom

Postcode: CV34 6WE

DJ Fang

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Other Products from HYCOR Biomedical Inc. (1)

Chemiluminescent immunoassay analyser IVD

Type: In Vitro Diagnostic Device

Registered: Nov 26, 2024

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Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration

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