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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.

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In Vitro Diagnostic Device
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Trypanosoma cruzi immunoglobulin G (IgG) antibody IVD, kit, enzyme immunoassay (EIA)
MHRA Device ID: 129586โ€ขRef: 129586

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

Manufacturer Information

Address

Riobamba 2944

Rosario, Argentina

Created Date

Dec 30, 2021

Authorized Representative

Relationship Type

UK Responsible Person

Address

Beaver House, 23-38 Hythe Bridge Street

Oxford, England, United Kingdom

Postcode: OX1 2EP

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