STRAUMANN® JASON® MEMBRANE
Mexico·Clase III·IV. DENTAL SUPPLIES·MANOHAY MÉXICO, S.A DE C.V.·Registered February 01, 2018ES INDICADA PARA TEJIDO GUIADO DEMORADO O INMEDIATO Y EN LA REGENERACIÓN DE HUESO
IT IS INDICATED FOR DELAYED OR IMMEDIATE GUIDED TISSUE AND IN BONE REGENERATION
- 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
- Analysis ID
- 301C2018 SSA
- Registration Date
- February 01, 2018
- Name (Spanish)
- MANOHAY MÉXICO, S.A DE C.V.
- Name (English)
- MANOHAY MÉXICO, S.A DE C.V.
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.