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STRAUMANN® JASON® MEMBRANE - COFEPRIS Registration 301C2018 SSA

Access comprehensive regulatory information for STRAUMANN® JASON® MEMBRANE (STRAUMANN® JASON® MEMBRANE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 301C2018 SSA and manufactured by MANOHAY MÉXICO, S.A DE C.V.. The device was registered on February 01, 2018.

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 III
301C2018 SSA
STRAUMANN® JASON® MEMBRANE
COFEPRIS Analysis ID: 301C2018 SSA
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Product Use / Uso del Producto
Spanish

ES INDICADA PARA TEJIDO GUIADO DEMORADO O INMEDIATO Y EN LA REGENERACIÓN DE HUESO

English

IT IS INDICATED FOR DELAYED OR IMMEDIATE GUIDED TISSUE AND IN BONE REGENERATION

Device Classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
IV. INSUMOS DE USO ODONTOLÓGICO
Product Type (English)
IV. DENTAL SUPPLIES
Trade Name (Spanish)
MEMBRANA DE COLÁGENO
Trade Name (English)
COLLAGEN MEMBRANE
Registration Information
Analysis ID
301C2018 SSA
Registration Date
February 01, 2018
Manufacturer / Fabricante
Name (English)
MANOHAY MÉXICO, S.A DE C.V.