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I-FIX® - COFEPRIS Registration 623C2022 SSA

Access comprehensive regulatory information for I-FIX® (I-FIX®) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 623C2022 SSA and manufactured by VAMASA, S.A. DE C.V.. The device was registered on July 15, 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
623C2022 SSA
I-FIX®
COFEPRIS Analysis ID: 623C2022 SSA
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Product Use / Uso del Producto
Spanish

PARA USO DURANTE LOS PROCEDIMIENTOS DERESTAURACIÓN DE DIENTESPARA LA CEMENTACIÓN DECORONAS,PUENTES,INLAYS,ONLAYS,BRACKETSYBANDASDE ORTODONCIA.

English

FOR USE DURING TOOTH RESTORATION PROCEDURES FOR CEMENTING ORTHODONTIC CROWNS, BRIDGES, INLAYS, ONLAYS, BRACKETS, AND BANDS.

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)
CEMENTO DE IONOMERO DEVIDRIO
Trade Name (English)
CEMENTO DE IONOMERO DEVIDRIO
Registration Information
Analysis ID
623C2022 SSA
Registration Date
July 15, 2022
Manufacturer / Fabricante
Name (Spanish)
VAMASA, S.A. DE C.V.
Name (English)
VAMASA, S.A. DE C.V.