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ANVISA registration 80384729014Active

Resin Modified Glass Ionomer

ANVISA Registration Number: 80384729014GC SOUTH AMERICA COMÉRCIO DE PRODUTOS DENTAIS LTDAGC R&D CORPORATION.Risk Class II
Verified
Device names
Technical name
Resin Modified Glass Ionomer
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PT: Ionomero de Vidro Modificado por Resina
Commercial name
Equia LC One
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Risk class
Class II
Registration details
Registration Number
80384729014
Process Number
25351086359202573
CNPJ
08279999000161
Company information
Registration Holder
GC SOUTH AMERICA COMÉRCIO DE PRODUTOS DENTAIS LTDA
Manufacturer
GC R&D CORPORATION.
Manufacturing Country
Japan
PT: JAPÃO
Dates and status
Publication Date
Jun 09, 2025
Validity
VIGENTE
Last Updated
08/18/2026 19:00:00
About this record

Access comprehensive regulatory information for Resin Modified Glass Ionomer in Brazil's medical device market through Pure Global AI's free database. This Risk Class II medical device is registered under ANVISA number 80384729014 and manufactured by GC R&D CORPORATION.. The registration is held by GC SOUTH AMERICA COMÉRCIO DE PRODUTOS DENTAIS 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.