SISTEMA DE STENT PERIFÉRICO AUTOEXPANSIBLE DE NITINOL, ASTRON PULSAR - COFEPRIS Registration 2088C2019 SSA
Access comprehensive regulatory information for SISTEMA DE STENT PERIFÉRICO AUTOEXPANSIBLE DE NITINOL, ASTRON PULSAR (NITINOL SELF-EXPANDING PERIPHERAL STENT SYSTEM, ASTRON PULSAR) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 2088C2019 SSA and manufactured by LEVBETH MEDICAL S.A. DE C.V.. The device was registered on November 06, 2019.
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.
EL SISTEMA DE STENT AUTOEXPANSIBLE ASTRON PULSAR ESTÁ INDICADO PARA UTILIZARSE EN PACIENTES CON ENFERMEDAD ATEROSCLERÓTICA DE LAS ARTERIAS FEMORALES E INFRAPOPLÍTEAS, Y PARA EL TRATAMIENTO DE PACIENTES EN LOS QUE LA ANGIOPLASTIA TRANSLUMINAL PERCUTÁNEA (A
THE ASTRON PULSAR SELF-EXPANDING STENT SYSTEM IS INDICATED FOR USE IN PATIENTS WITH ATHEROSCLEROTIC DISEASE OF THE FEMORAL AND INFRAPOPLITEAL ARTERIES, AND FOR THE TREATMENT OF PATIENTS UNDERGOING PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (A