Varicella-zoster virus (VZV) immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration
Varicella-zoster virus (VZV) immunoglobulin G (IgG) 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 125026. The device is manufactured by Clark Laboratories, INC., dba Trinity Biotech USA from United States, 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
Varicella-zoster virus (VZV) immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Type
IVD General
Date Registered
Nov 26, 2024
Last Updated
Sep 27, 2024
Address
Clark Laboratories, INC., dba Trinity Biotech USA 2823 Girts Road
Jamestown, NY, United States
Created Date
Dec 21, 2021
Relationship Type
Address
Maidstone Innovation Centre Gidds Pond Way
Maidstone, Kent, England, United Kingdom
Postcode: ME14 5FY
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