BESMOOTH SISTEMA DE STENT PERIFÉRICO - COFEPRIS Registration 425C2018 SSA
Access comprehensive regulatory information for BESMOOTH SISTEMA DE STENT PERIFÉRICO (BESMOOTH PERIPHERAL STENT SYSTEM) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 425C2018 SSA and manufactured by LEVBETH MEDICAL S.A. DE C.V.. The device was registered on February 16, 2018.
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.
ESTÁ INDICADO PARA EL TRATAMIENTO DE LESIONES ATEROSCLERÓTICAS DE NOVO O REESTENÓTICAS EN ARTERIAS PERIFÉRICAS PROTEGIDAS
IT IS INDICATED FOR THE TREATMENT OF DE NOVO ATHEROSCLEROTIC OR RESTENOTIC LESIONS IN PROTECTED PERIPHERAL ARTERIES