Legionella pneumophila immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration
Legionella pneumophila immunoglobulin M (IgM) 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 90276. 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.
Device Type
In Vitro Diagnostic Device
Devices
Legionella pneumophila immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
Type
IVD General
Date Registered
Jul 12, 2021
Last Updated
Oct 13, 2022
Relationship Type
Address
Ash House Ash Road New Ash Green
Longfield, Kent, United Kingdom
Postcode: DA3 8JD
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