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 170258. The device is manufactured by Guangzhou Wondfo Biotech Co., Ltd. from China, classified as In Vitro Diagnostic Device. The authorized representative in the UK is Qarad 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
Allergen-specific/total immunoglobulin E (IgE) antibody IVD, kit, fluorescent immunoassay
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Jul 31, 2024
Address
No.8 Lizhishan Road, Science City, Huangpu District
Guangzhou, China
Created Date
Mar 7, 2021
Name
Qarad UK Ltd.Relationship Type
Address
8 Northumberland Ave
Westminster, London , England, United Kingdom
Postcode: WC2N 5BY
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