DYNAMESH®-ENDOLAP 3D
DYNAMESH®-ENDOLAP 3D SIRVE PARAREFORZAR ESTRUCTURAS DE TEJIDOCONJUNTIVO EN LA REGIÓN INGUINAL.
DYNAMESH-ENDOLAP® 3D SERVES TO REINFORCE CONNECTIVE TISSUE STRUCTURES IN THE INGUINAL REGION.
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- V. MATERIALES QUIRÚRGICOS Y DE CURACIÓN
- Product Type (English)
- V. SURGICAL AND HEALING MATERIALS
- Trade Name (Spanish)
- MALLA PARA REPARACIÓN DE HERNIAINGUINAL
- Trade Name (English)
- MESH FOR HERNIAINGUINAL REPAIR
- Analysis ID
- 1605C2021 SSA
- Registration Date
- October 14, 2021
- Name (Spanish)
- ISA HEALTH S.A. DE C.V.
- Name (English)
- ISA HEALTH S.A. DE C.V.
Access comprehensive regulatory information for DYNAMESH®-ENDOLAP 3D (DYNAMESH-ENDOLAP® 3D) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1605C2021 SSA and manufactured by ISA HEALTH S.A. DE C.V.. The device was registered on October 14, 2021.
This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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.