I-ZOEN®
Mexico·Clase II·IV. DENTAL SUPPLIES·VAMASA, S.A. DE C.V.·Registered July 11, 2022RESINAMODIFICADACONCEMENTODENTALABASEDEÓXIDO DE ZINC-EUGENOL
RESINMODIFIEDWITH CEMENTDENTALZINC OXIDE-EUGENOL BASE
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- IV. INSUMOS DE USO ODONTOLÓGICO
- Product Type (English)
- IV. DENTAL SUPPLIES
- Trade Name (Spanish)
- RESINA MODIFICADA CONCEMENTODENTALABASEDEÓXIDO DE ZINC-EUGENOL
- Trade Name (English)
- CEMENT MODIFIED RESINDENTALZINC OXIDE-EUGENOL BASE
- Analysis ID
- 586C2022 SSA
- Registration Date
- July 11, 2022
- Name (Spanish)
- VAMASA, S.A. DE C.V.
- Name (English)
- VAMASA, S.A. DE C.V.
Access comprehensive regulatory information for I-ZOEN® (I-KISS®) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 586C2022 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.