MICROCATÉTER VIA™ - COFEPRIS Registration 50C2020 SSA
Access comprehensive regulatory information for MICROCATÉTER VIA™ (MICROCATÉTER VIA™) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 50C2020 SSA and manufactured by LEVBETH MEDICAL, S.A. DE C.V.. The device was registered on January 15, 2020.
This page provides complete registration details including product type (V. SURGICAL AND HEALING MATERIALS), 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.
MICROCATÉTER VIA™, EL MICROCATÉTER VIAESTÁ INDICADO PARA LA INTRODUCCIÓN DEDISPOSITIVOS INTERVENCIONISTAS NOLÍQUIDOS (COMO STENTS Y DESVIADORES DEFLUJO) Y PARA LA INFUSIÓN DE AGENTESDIAGNÓSTICOS(COMOMEDIOSDECONTRASTE)OTERAPÉUTICOSENLANEUROVASCULATURA,LA VASCULATURA PERIFÉRICA Y LAVASCULATURA CORONARIA.
MICROCATHETER VIA, THE MICROCATHETER VIA™, IS INDICATED FOR THE INTRODUCTION OF NON-LIQUID INTERVENTIONAL DEVICES (SUCH AS STENTS AND FLOW DIVERTERS) AND FOR THE INFUSION OF DIAGNOSTIC AGENTS (SUCH AS CONTRAST MEDIA) OR THERAPEUTIC AGENTS IN NEUROVASCULATURE, PERIPHERAL VASCULATURE AND CORONARY LAVASCULATURE.