SISTEMA DE STENT URETERAL (URS) ALLIUM® - COFEPRIS Registration 2040C2018 SSA
Access comprehensive regulatory information for SISTEMA DE STENT URETERAL (URS) ALLIUM® (ALLIUM® URETERAL STENT SYSTEM (URS)) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 2040C2018 SSA and manufactured by LEVBETH MEDICAL, S.A. DE C.V.. The device was registered on August 20, 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.
SISTEMA DE STENT URETERAL (URS) ALLIUM®, MANEJO DE OBSTRUCCIÓN DE LA SALIDA VESICAL (BOO) CAUSADA POR: 1. CIRUGÍA DE PRÓSTATA 2. PROSTATECTOMÍA Y CISTOPROSTATECTOMÍA RADICALES 3. ESTENOSIS URETRAL POSTERIOR
ALLIUM® URETERAL STENT SYSTEM (URS), MANAGEMENT OF BLADDER OUTLET OBSTRUCTION (BOO) CAUSED BY: 1. PROSTATE SURGERY 2. RADICAL PROSTATECTOMY AND CYSTOPROSTATECTOMY 3. POSTERIOR URETHRAL STRICTURE