Trypanosoma cruzi immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA) - UK MHRA Medical Device Registration
Trypanosoma cruzi 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 129586. The device is manufactured by Wiener Laboratorios S.A.I.C from Argentina, classified as In Vitro Diagnostic Device. The authorized representative in the UK is MT Promedt Consulting 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
Trypanosoma cruzi immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
Type
IVD General
Date Registered
Nov 19, 2024
Last Updated
Oct 25, 2024
Relationship Type
Address
Beaver House, 23-38 Hythe Bridge Street
Oxford, England, United Kingdom
Postcode: OX1 2EP
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