MICROCATÉTER WEDGE - COFEPRIS Registration 427C2020 SSA
Access comprehensive regulatory information for MICROCATÉTER WEDGE (MICROCATÉTER WEDGE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 427C2020 SSA and manufactured by LEVBETH MEDICAL, S.A. DE C.V.. The device was registered on April 23, 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.
EL MICROCATÉTER WEDGE ESTÁ PREVISTOPARA EL USO INTRAVASCULAR GENERAL,INCLUYENDO LA VASCULATURA PERIFÉRICA,CORONARIA Y NEURONAL PARA LA INFUSIÓNDEAGENTESDIAGNÓSTICOS,COMOMEDIOSDECONTRASTE,YPARAASISTIRENLAAPLICACIÓNDE DISPOSITIVOS DE INTERVENCIÓN, TALESCOMO EL CATÉTER SOFIA 6F, EN LANEUROVASCULATURA.
THE WEDGE MICROCATHETER IS INTENDED FOR GENERAL INTRAVASCULAR USE, INCLUDING THE PERIPHERAL, CORONARY AND NEURONAL VASCULATURE FOR THE INFUSION OF DIAGNOSTIC AGENTS, SUCH AS CONTRAST MEDIA, AND TO ASSIST IN THE APPLICATION OF INTERVENTIONAL DEVICES, SUCH AS THE SOFIA 6F CATHETER, IN THE NEUROVASCULATURE.