REVERSE TRIIODOTHYRONINE (T3) - ANVISA Registration 80464810374
Access comprehensive regulatory information for REVERSE TRIIODOTHYRONINE (T3) in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80464810374 and manufactured by WUHAN HUAMEI BIOTECH CO., LTD.. The registration is held by ARGOSLAB DISTRIBUIDORA DE PRODUTOS PARA LABORATÓRIOS LTDA with validity until currently active (VIGENTE).
This page provides complete technical specifications for this device, regulatory compliance details, 5 similar products found using AI-powered semantic search, 5 companies making the same product including SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD., EUROIMMUN BRASIL MEDICINA DIAGNOSTICA LTDA, and 5 recent registrations in the same technical category. Pure Global AI offers free access to over 100,000+ Brazilian medical device registrations, helping global MedTech companies navigate ANVISA regulations, identify competitors, and discover partnership opportunities efficiently.

Janaina dos Santos de Miranda
🇧🇷 Brazil Regulatory Expert
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Registration Details
80464810374
25351148177201436
09377976000152
Company Information
Dates and Status
Apr 22, 2014
VIGENTE
09/18/2025 19:00:01
FREE TRIIODOTHYRONINE (T3)
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TRIIODOTIRONINA (T3) REVERSA
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TRIIODOTIRONINA (T3) REVERSA
Família T3 Reversa (CLIA) – rT3
SHENZHEN MINDRAY BIO-MEDICAL ELECTRONICS CO., LTD
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Jun 02, 2021
TRIIODOTIRONINA (T3) REVERSA
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EUROIMMUN AG
10338930243
Dec 10, 2020