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DYNAMESH®-ENDOLAP 3D - COFEPRIS Registration 1605C2021 SSA

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.

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COFEPRIS Official Data
Clase III
1605C2021 SSA
DYNAMESH®-ENDOLAP 3D
COFEPRIS Analysis ID: 1605C2021 SSA
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Product Use / Uso del Producto
Spanish

DYNAMESH®-ENDOLAP 3D SIRVE PARAREFORZAR ESTRUCTURAS DE TEJIDOCONJUNTIVO EN LA REGIÓN INGUINAL.

English

DYNAMESH-ENDOLAP® 3D SERVES TO REINFORCE CONNECTIVE TISSUE STRUCTURES IN THE INGUINAL REGION.

Device Classification
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
Registration Information
Analysis ID
1605C2021 SSA
Registration Date
October 14, 2021
Manufacturer / Fabricante
Name (English)
ISA HEALTH S.A. DE C.V.