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CEMENTO DE IONÓMERO DE VIDRIO MODIFICADO CON RESINA - COFEPRIS Registration 0622C2022 SSA

Access comprehensive regulatory information for CEMENTO DE IONÓMERO DE VIDRIO MODIFICADO CON RESINA (CEMENTO DE IONÓMERO DE VIDRIO MODIFICADO CON RESINA) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 0622C2022 SSA and manufactured by VAMASA, S.A. DE C.V.. The device was registered on July 18, 2022.

This page provides complete registration details including product type (IV. Insumos de uso odontológico), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.

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COFEPRIS Official Data
Clase II
0622C2022 SSA
CEMENTO DE IONÓMERO DE VIDRIO MODIFICADO CON RESINA
COFEPRIS Analysis ID: 0622C2022 SSA
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Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
IV. Insumos de uso odontológico
Product Type (English)
IV. Insumos de uso odontológico
Trade Name (Spanish)
I-FIX®PLUS
Trade Name (English)
I-FIX®PLUS
Registration Information
Analysis ID
0622C2022 SSA
Registration Date
July 18, 2022
Manufacturer / Fabricante
Name (Spanish)
VAMASA, S.A. DE C.V.
Name (English)
VAMASA, S.A. DE C.V.