CROSSWAY CATÉTER DEDILATACIÓN PARA ACTP - COFEPRIS Registration 784C2021 SSA

Access comprehensive regulatory information for CROSSWAY CATÉTER DEDILATACIÓN PARA ACTP (CROSSWAY DEDILATATION CATHETER FOR PTCA) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 784C2021 SSA and manufactured by MEDSTENT, S.A. DE C.V.. The device was registered on March 05, 2021.

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.