MAMBATM - COFEPRIS Registration 2015C2019 SSA
Access comprehensive regulatory information for MAMBATM (MAMBATM) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 2015C2019 SSA and manufactured by BOSTON SCIENTIFIC DE MÉXICO, S.A. DE C.V.. The device was registered on October 18, 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 MICROCATÉTERES MAMBATM Y MAMBATM FLEX ESTÁN DISEÑADOS PARA SERVIR DE SOPORTE PARA FACILITAR LA COLOCACIÓN DE GUÍAS EN LAS VASCULATURAS CORONARIAS Y PUEDEN UTILIZARSE PARA INTERCAMBIAR UNA GUÍA POR OTRA.
MAMBATM AND MAMBATM FLEX MICROCATHETERS ARE DESIGNED TO SUPPORT EASY PLACEMENT OF GUIDES IN CORONARY VASCULATURES AND CAN BE USED TO SWAP ONE GUIDE FOR ANOTHER.