United Kingdom MHRA device registration 194606

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

United Kingdom·In Vitro Diagnostic Device·HYCOR Biomedical Inc.·Registered Nov 26, 2024

Registration details

Device ID: 194606
MHRA Reference Number: 194606
Date Registered: Nov 26, 2024
Last Updated: Jun 5, 2024

Device classification

Device Type: In Vitro Diagnostic Device
Devices: Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, enzyme immunoassay (EIA)
Type: IVD General

Manufacturer

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

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About this record

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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