WOLVERINE CORONARY CUTTINGBALLON MONORAIL - COFEPRIS Registration 862C2021 SSA
Access comprehensive regulatory information for WOLVERINE CORONARY CUTTINGBALLON MONORAIL (WOLVERINE CORONARY CUTTINGBALLON MONORAIL) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 862C2021 SSA and manufactured by BOSTONSCIENTIFICDEMÉXICO, S.A. DE C.V.. The device was registered on May 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.
EL DISPOSITIVO WOLVERINE CUTTINGBALLOON ESTÁ INDICADO PARA PACIENTESCON ENFERMEDADES VASCULARESCORONARIAS APTOS PARA CIRUGÍA DEINJERTO DE DERIVACIÓN DE LA ARTERIACORONARIA,ENCASODEQUESEREQUIERACONURGENCIA,CONELFINDEMEJORARLAPERFUSIÓN MIOCÁRDICA.
THE WOLVERINE CUTTINGBALLOON DEVICE IS INDICATED FOR PATIENTS WITH CORONARY VASCULAR DISEASES SUITABLE FOR CORONARY ARTERY BYPASS GRAFT SURGERY, IF REQUIRED URGENTLY, IN ORDER TO IMPROVE MYOCARDIAL PERFUSION.