Helicobacter pylori immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration
Helicobacter pylori immunoglobulin A (IgA) 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 150651. The device is manufactured by VicTorch Meditek, Inc. from United States, classified as In Vitro Diagnostic Device. The authorized representative in the UK is UKCApartner4U 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
Helicobacter pylori immunoglobulin A (IgA) antibody IVD, kit, enzyme immunoassay (EIA)
Type
IVD General
Date Registered
Jun 30, 2022
Last Updated
Apr 13, 2023
Address
6888 Nancy Ridge Drive
San Diego, California, United States
Created Date
Jun 30, 2022
Relationship Type
Address
7 CAMPION WAY
BINGHAM, NOTTINGHAM, England, United Kingdom
Postcode: NG13 8 TR
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