SISTEMA DE STENT PERIFÉRICO PRO-KINETIC ENERGY EXPLORER
EL SISTEMA DE STENT PRO-KINETIC ENERGY EXPLORER ESTÁ INDICADO PARA MEJORAR RESULTADOS ANGIOGRÁFICOS DEFICIENTES (ESTENOSIS RESIDUAL ≥ 50%) O DISECCIONES LIMITADORAS DEL FLUJO DESPUÉS DE LA ATP DE LESIONES ATEROSCLERÓTICAS DE LAS ARTERIAS INFRAPOPLIT
THE PRO-KINETIC ENERGY EXPLORER STENT SYSTEM IS INDICATED TO IMPROVE POOR ANGIOGRAPHIC OUTCOMES (RESIDUAL STENOSIS ≥ 50%) OR FLOW-LIMITING DISSECTIONS AFTER ATP OF ATHEROSCLEROTIC LESIONS OF THE INFRAPOPLIT ARTERIES
- 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 PERIFÉRICO
- Trade Name (English)
- PERIPHERAL STENT SYSTEM
- Analysis ID
- 2089C2019 SSA
- Registration Date
- November 06, 2019
- Name (Spanish)
- LEVBETH MEDICAL S.A. DE C.V.
- Name (English)
- LEVBETH MEDICAL S.A. DE C.V.
Access comprehensive regulatory information for SISTEMA DE STENT PERIFÉRICO PRO-KINETIC ENERGY EXPLORER (PRO-KINETIC ENERGY EXPLORER 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 2089C2019 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.