Mexico COFEPRIS registration 2040C2018 SSA

SISTEMA DE STENT URETERAL (URS) ALLIUM®

EN: ALLIUM® URETERAL STENT SYSTEM (URS)
Mexico flagMexico·Clase III·II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS·LEVBETH MEDICAL, S.A. DE C.V.·Registered August 20, 2018
Product Use / Uso del Producto
Spanish

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

English

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

Device classification
Risk Class / Clase de Riesgo
Clase III
Product Type (Spanish)
II. PROTESIS, ÓRTESIS Y AYUDAS FUNCIONALES
Product Type (English)
II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
Trade Name (Spanish)
SISTEMA DE STENT URETERAL
Trade Name (English)
URETERAL STENT SYSTEM
Registration information
Analysis ID
2040C2018 SSA
Registration Date
August 20, 2018
Manufacturer / Fabricante
Name (English)
LEVBETH MEDICAL, S.A. DE C.V.
About this record

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.

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