Multiple Borrelia species immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration
Multiple Borrelia species 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 142734. The device is manufactured by Mikrogen GmbH from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is IVDeology UKRP Ltd.
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
Multiple Borrelia species immunoglobulin M (IgM) antibody IVD, kit, enzyme immunoassay (EIA)
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Sep 20, 2024
Name
Mikrogen GmbHAddress
Anna-Sigmund-Str 10 Neuried
Mรผnchen, Oberbayern, Germany
Created Date
Mar 31, 2022
Relationship Type
Address
Maidstone Innovation Centre Gidds Pond Way
Maidstone, Kent, England, United Kingdom
Postcode: ME14 5FY
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