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ANVISA registration 80535240072Active

AUTOTESTE PARA ANTICORPO PARA DOENÇA CELÍACA

ANVISA Registration Number: 80535240072CHEMBIO DIAGNOSTICS BRAZIL LTDA.CHEMBIO DIAGNOSTICS BRAZIL LTDA.Risk Class II
Verified
Device names
Technical name
AUTOTESTE PARA ANTICORPO PARA DOENÇA CELÍACA
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Commercial name
Biosynex Teste de Glúten
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Risk class
Class II
Registration details
Registration Number
80535240072
Process Number
25351400873202445
CNPJ
09449181000102
Company information
Registration Holder
CHEMBIO DIAGNOSTICS BRAZIL LTDA.
Manufacturer
CHEMBIO DIAGNOSTICS BRAZIL LTDA.
Manufacturing Country
Brazil
PT: BRASIL
Dates and status
Publication Date
Dec 23, 2024
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for AUTOTESTE PARA ANTICORPO PARA DOENÇA CELÍACA in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80535240072 and manufactured by CHEMBIO DIAGNOSTICS BRAZIL LTDA.. The registration is held by CHEMBIO DIAGNOSTICS BRAZIL 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.