SISTEMA DE STENT PERIFÉRICO AUTOEXPANSIBLE DE NITINOL, PULSAR-35 - COFEPRIS Registration 1311C2019 SSA
Access comprehensive regulatory information for SISTEMA DE STENT PERIFÉRICO AUTOEXPANSIBLE DE NITINOL, PULSAR-35 (NITINOL SELF-EXPANDING PERIPHERAL STENT SYSTEM, PULSAR-35) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1311C2019 SSA and manufactured by LEVBETH MEDICAL S.A. DE C.V.. The device was registered on July 16, 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.
PARA UTILIZARSE EN PACIENTES CON ENFERMEDAD ATEROSCLERÓTICA DE LAS ARTERIAS FEMORALES Y POPLÍTEAS PROXIMALES, EN PARTICULAR PARA EL TRATAMIENTO DE PACIENTES EN LOS QUE LA ANGIOPLASTIA TRANSLUMINAL PERCUTÁNEA (ATP) HAYA DADO RESULTADOS INSUFICIENTES, COMO,
FOR USE IN PATIENTS WITH ATHEROSCLEROTIC DISEASE OF THE FEMORAL AND PROXIMAL POPLITEAL ARTERIES, IN PARTICULAR FOR THE TREATMENT OF PATIENTS IN WHOM PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (PTA) HAS YIELDED INSUFFICIENT RESULTS, SUCH AS,