United Kingdom MHRA device registration 140136

Interferon IVD, kit, enzyme immunoassay (EIA)

United Kingdom·In Vitro Diagnostic Device·Lionex GmbH·Registered Nov 26, 2024

Registration details

Device ID: 140136
MHRA Reference Number: 140136
Date Registered: Nov 26, 2024
Last Updated: Nov 15, 2023

Device classification

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

Manufacturer

Name: Lionex GmbH
Address: Salzdahlumer Str. 196
Gebäude 1A, Germany
Created Date: Mar 15, 2022

Authorized Representative

Name: A. Menarini Diagnostics Ltd.
Relationship Type: UK Responsible Person
Address: 405 Wharfedale Road
Wokingham, Berkshire, England, United Kingdom
Postcode: RG41 5RA

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About this record

Interferon IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 140136. The device is manufactured by Lionex GmbH from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is A. Menarini Diagnostics Ltd..

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