REACT™ CATHETER - COFEPRIS Registration 2115C2019 SSA
Access comprehensive regulatory information for REACT™ CATHETER (REACT™ CATHETER) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 2115C2019 SSA and manufactured by KENDALL DE MÉXICO, S.A. DE C.V.. The device was registered on November 08, 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.
LOS CÁTETERES REACT™ ESTÁN INDICADOS PARA LA INTRODUCCIÓN DE DISPOSITIVOS INTERVENCIONISTAS Y DE DIAGNÓSTICO EN LA VASCULATURA PERIFÉRICA Y EN LA NEUROVASCULATURA. LOS CÁTETERES REACT™ TAMBIÉN ESTÁN INDICADOS PARA LA ELIMINACIÓN Y ASPIRACIÓN DE ÉMBOLOS
REACT™ CATHETERS ARE INDICATED FOR THE INTRODUCTION OF INTERVENTIONAL AND DIAGNOSTIC DEVICES IN THE PERIPHERAL VASCULATURE AND NEUROVASCULATURE. REACT™ CATHETERS ARE ALSO INDICATED FOR THE REMOVAL AND ASPIRATION OF EMBOLI