KIT DE MALLA EN FORMA DE Y UPSYLON - COFEPRIS Registration 2178C2019 SSA
Access comprehensive regulatory information for KIT DE MALLA EN FORMA DE Y UPSYLON (Y-SHAPED MESH KIT UPSYLON) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 2178C2019 SSA and manufactured by BOSTON SCIENTIFIC DE MÉXICO, S.A. DE C.V.. The device was registered on November 25, 2019.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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.
EL KIT DE MALLA EN FORMA DE Y UPSYLON ESTÁ INDICADO PARA SER UTILIZADO COMO MATERIAL DE APOYO DURANTE LA SACROCOLPOSUSPENSIÓN / SACROCOLPOPEXIA (LAPAROTOMÍA, ABORDAJE LAPAROSCÓPICO O ROBÓTICO) EN DONDE SE GARANTICE EL TRATAMIENTO QUIRÚRGICO PARA EL PROLAP
THE Y-SHAPED MESH KIT UPSYLON IS INDICATED TO BE USED AS A SUPPORT MATERIAL DURING SACROCOLPOSUSPENSION / SACROCOLPOPEXY (LAPAROTOMY, LAPAROSCOPIC OR ROBOTIC APPROACH) WHERE SURGICAL TREATMENT FOR PROLAP IS GUARANTEED