PARIETENE DS COMPOSITE MESH - COFEPRIS Registration 608C2019 SSA
Access comprehensive regulatory information for PARIETENE DS COMPOSITE MESH (PARIETENE DS COMPOSITE 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 608C2019 SSA and manufactured by KENDALL DE MÉXICO, S.A. DE C.V.. The device was registered on March 26, 2019.
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.
LA MALLA COMPUESTA PARIETENE™DS ESTÁ INDICADA PARA EL REFORZAMIENTO DE LA PARED ABDOMINAL DEL TEJIDO SUAVE DONDE EXISTA DEBILIDAD Y PARA LA REPARACIÓN DE HERNIAS VENTRALES.
THE COMPOSITE MESH PARIETENE™DS IS INDICATED FOR THE REINFORCEMENT OF THE ABDOMINAL WALL OF SOFT TISSUE WHERE THERE IS WEAKNESS AND FOR THE REPAIR OF VENTRAL HERNIAS.