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ANVISA registration 80384720035Active

Resin Modified Glass Ionomer

ANVISA Registration Number: 80384720035GC SOUTH AMERICA COMÉRCIO DE PRODUTOS DENTAIS LTDAGC AMERICA INC.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 FORTE
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Risk class
Class II
Registration details
Registration Number
80384720035
Process Number
25351509280201604
CNPJ
08279999000161
Company information
Registration Holder
GC SOUTH AMERICA COMÉRCIO DE PRODUTOS DENTAIS LTDA
Manufacturer
GC AMERICA INC.
Manufacturing Country
United States
PT: ESTADOS UNIDOS DA AMÉRICA
Dates and status
Publication Date
May 29, 2017
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 80384720035 and manufactured by GC AMERICA INC.. 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.