United Kingdom MHRA device registration 90272

Influenza B virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

United Kingdom flagUnited Kingdom·In Vitro Diagnostic Device·Virion\Serion GmbH·Registered Jul 12, 2021
Registration details
Device ID
90272
MHRA Reference Number
90272
Date Registered
Jul 12, 2021
Last Updated
Oct 13, 2022
Device classification
Device Type
In Vitro Diagnostic Device
Devices
Influenza B virus immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Type
IVD General
Manufacturer
Address
Friedrich-Bergius-Ring 19
Wurzburg, Germany
Created Date
Jul 12, 2021
Authorized Representative
Relationship Type
UK Responsible Person
Address
Ash House Ash Road New Ash Green
Longfield, Kent, United Kingdom
Postcode: DA3 8JD
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About this record

Influenza B virus immunoglobulin G (IgG) 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 90272. The device is manufactured by Virion\Serion GmbH from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Launch Diagnostics 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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