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PARIETENE™ MACROPOROUS MESH. - COFEPRIS Registration 1973C2018 SSA

Access comprehensive regulatory information for PARIETENE™ MACROPOROUS MESH. (PARIETENE™ MACROPOROUS MESH.) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1973C2018 SSA and manufactured by KENDALL DE MÉXICO, S.A. DE C.V.. The device was registered on August 09, 2018.

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
1973C2018 SSA
PARIETENE™ MACROPOROUS MESH.
COFEPRIS Analysis ID: 1973C2018 SSA
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Product Use / Uso del Producto
Spanish

LA MALLA PARIETENE™ MACROPOROUS MESH ESTÁ PREVISTO PARA EL REFORZAMIENTO DE TEJIDO SUAVE DONDE EXISTE DEBILIDAD DURANTE LA REPARACIÓN QUIRÚRGICA Y ES INDICADO PARA LA REPARACIÓN DE HERNIAS U OTRAS DEFICIENCIAS FASCIALES QUE REQUIEREN LA ADICCIÓN DE UN MAT

English

MACROPOROUS PARIETENE™ MESH IS INTENDED FOR THE REINFORCEMENT OF SOFT TISSUE WHERE THERE IS WEAKNESS DURING SURGICAL REPAIR AND IS INDICATED FOR THE REPAIR OF HERNIAS OR OTHER FASCIAL DEFICIENCIES THAT REQUIRE THE ADDITION OF A MAT

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 QUIRÚRGICA NO ABSORBIBLE DE POLIPROPILENO MONOFILAMENTOSA MACROPOROSA.
Trade Name (English)
NON-ABSORBABLE SURGICAL MESH OF MACROPOROUS MONOFILAMENTOUS POLYPROPYLENE.
Registration Information
Analysis ID
1973C2018 SSA
Registration Date
August 09, 2018
Manufacturer / Fabricante
Name (English)
KENDALL DE MÉXICO, S.A. DE C.V.