GUÍA THRUWAY - COFEPRIS Registration 1298C2019 SSA
Access comprehensive regulatory information for GUÍA THRUWAY (THRUWAY GUIDE) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1298C2019 SSA and manufactured by BOSTON SCIENTIFIC DE MÉXICO, S.A. DE C.V.. The device was registered on July 15, 2019.
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.
LA GUÍA THRUWAY™ FACILITA LA COLOCACIÓN DE UN CATÉTER DURANTE LOS PROCEDIMIENTOS DE DIAGNÓSTICO O LOS PROCEDIMIENTOS INTRAVASCULARES PERIFÉRICOS INTERVENCIONISTAS, INCLUYENDO, ENTRE OTROS, LAS INTERVENCIONES RENALES. SE PUEDE EJERCER TORSIÓN SOBRE LA GUÍA
THE THRUWAY™ GUIDE FACILITATES CATHETER PLACEMENT DURING DIAGNOSTIC PROCEDURES OR INTERVENTIONAL PERIPHERAL INTRAVASCULAR PROCEDURES, INCLUDING, BUT NOT LIMITED TO, RENAL INTERVENTIONS. TWISTING CAN BE EXERTED ON THE GUIDE