Neutrophil elastase IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration
Neutrophil elastase IVD, kit, enzyme immunoassay (EIA) is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 148046. The device is manufactured by Immundiagnostik AG from Germany, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qserve Group UK, 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
Neutrophil elastase IVD, kit, enzyme immunoassay (EIA)
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Oct 31, 2024
Relationship Type
Address
49 Greek Street
London, England, United Kingdom
Postcode: W1D 4EG
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