XACT STENT CAROTIDEO - SISTEMA DE STENT CAROTIDEO - INVIMA Registration 1ed53480e7442c28d3b25caa84c5a705
Access comprehensive regulatory information for XACT STENT CAROTIDEO - SISTEMA DE STENT CAROTIDEO (XACT CAROTID STENT - CAROTID STENT SYSTEM) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 1ed53480e7442c28d3b25caa84c5a705 and manufactured by ABBOTT LABORATORIES DE COLOMBIA S.A.S.. The device was registered on May 28, 2034.
This page provides complete registration details including product type (SURGICAL DOCTOR), authorised information, and regulatory compliance data from the official Colombia INVIMA medical device database. Pure Global AI offers free access to Colombia's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate INVIMA regulations efficiently.
EL SISTEMA DE STENT CAROTÍDEO X.ACT™ ESTÁ INDICADO PARA USARSE EN PACIENTES CON ATEROESCLEROSIS DE LAS ARTERIAS CARÓTIDAS._x000D_ EL SISTEMA DE STENT CAROTÍDEO X.ACT ESTÁ INDICADO PARA USARSE JUNTO CON LOS SISTEMAS DE PROTECCIÓN FRENTE A EMBOLIAS (SPE) DE LA FAMILIA ACCUNET™ O EMBOSHIELD™ DE ABBOTT VASCULAR._x000D_
THE X.ACT™ CAROTID STENT SYSTEM IS INDICATED FOR USE IN PATIENTS WITH ATHEROSCLEROSIS OF THE CARÓTIDAS._x000D_ ARTERIES THE X.ACT CAROTID STENT SYSTEM IS INDICATED FOR USE IN CONJUNCTION WITH ABBOTT ACCUNET™ FAMILY EMBOLISM PROTECTION SYSTEMS (SPES) OR ABBOTT EMBOSHIELD™ VASCULAR._x000D_