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-LINER® - COFEPRIS Registration 587C2022 SSA

Access comprehensive regulatory information for -LINER® (-LINER®) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 587C2022 SSA and manufactured by VAMASA, S.A. DE C.V.. The device was registered on July 11, 2022.

This page provides complete registration details including product type (IV. DENTAL SUPPLIES), 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
587C2022 SSA
-LINER®
COFEPRIS Analysis ID: 587C2022 SSA
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Product Use / Uso del Producto
Spanish

CEMENTODEIONÓMERODEVIDRIOPARABASECAVITARIAENJERINGA,PUEDEUSARSECOMOBASECAVITARIAOPARARECUBRIR LA CAVIDAD ENTERA.

English

GLASSIONOMERCEMENTFORBASECAVITARIASYRINGE, CAN BE USED AS BASECAVITARY OR TO COAT THE ENTIRE CAVITY.

Device Classification
Risk Class / Clase de Riesgo
Clase II
Product Type (Spanish)
IV. INSUMOS DE USO ODONTOLÓGICO
Product Type (English)
IV. DENTAL SUPPLIES
Trade Name (Spanish)
LINER COMPOMERO DECURADO POR LUZI
Trade Name (English)
LUZI-CURED COMPOSITE LINER
Registration Information
Analysis ID
587C2022 SSA
Registration Date
July 11, 2022
Manufacturer / Fabricante
Name (Spanish)
VAMASA, S.A. DE C.V.
Name (English)
VAMASA, S.A. DE C.V.