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ANVISA registration 80102513523Active

REVERSE TRIIODOTHYRONINE (T3)

ANVISA Registration Number: 80102513523VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDASHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.Risk Class II
Verified
Device names
Technical name
REVERSE TRIIODOTHYRONINE (T3)
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PT: TRIIODOTIRONINA (T3) REVERSA
Commercial name
Maglumi Familia Rev T3 (CLIA)
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Risk class
Class II
Registration details
Registration Number
80102513523
Process Number
25351136217202564
CNPJ
04718143000194
Company information
Registration Holder
VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA
Manufacturer
SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.
Manufacturing Country
China
PT: CHINA, REPÚBLICA POPULAR
Dates and status
Publication Date
Sep 15, 2025
Status
Active
Official value: VIGENTE
About this record

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 80102513523 and manufactured by SHENZHEN NEW INDUSTRIES BIOMEDICAL ENGINEERING CO., LTD.. The registration is held by VR MEDICAL IMPORTADORA E DISTRIBUIDORA DE PRODUTOS MÉDICOS LTDA with validity until currently active (VIGENTE).

This page shows the facts attached to this official registry row. Exact-name links return deterministic registry matches; open-ended comparison and market analysis are handed to AI Search with this record's context, without asserting that similar names represent the same entity.