Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, fluorescent immunoassay - UK MHRA Medical Device Registration
Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, fluorescent immunoassay is a medical device registered with the UK's Medicines and Healthcare products Regulatory Agency (MHRA) under Device ID 193999. The device is manufactured by Vitrosens Biyoteknoloji A.S. from Turkey, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Pathaway Services 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
Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, fluorescent immunoassay
Type
IVD General
Date Registered
Nov 19, 2024
Last Updated
Jul 17, 2024
Address
Serifali Mah Sehit Sokak No: 17/A
Istanbul, Umraniye, Turkey
Created Date
Jul 17, 2023
Relationship Type
Address
Headlands House 1 Kings Court Kettering Parkway
Kettering, Northamptonshire, England, United Kingdom
Postcode: NN15 6WJ
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