United Kingdom MHRA device registration 125036

Epstein-Barr virus (EBV) immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)

United Kingdom flagUnited Kingdom·In Vitro Diagnostic Device·Clark Laboratories, INC., dba Trinity Biotech USA·Registered Nov 26, 2024
Registration details
Device ID
125036
MHRA Reference Number
125036
Date Registered
Nov 26, 2024
Last Updated
Sep 27, 2024
Device classification
Device Type
In Vitro Diagnostic Device
Devices
Epstein-Barr virus (EBV) immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Type
IVD General
Manufacturer
Address
Clark Laboratories, INC., dba Trinity Biotech USA 2823 Girts Road
Jamestown, NY, United States
Created Date
Dec 21, 2021
Authorized Representative
Relationship Type
UK Responsible Person
Address
Maidstone Innovation Centre Gidds Pond Way
Maidstone, Kent, England, United Kingdom
Postcode: ME14 5FY
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About this record

Epstein-Barr virus (EBV) 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 125036. 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.

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