ANACONDA (SISTEMA DE INJERTO ENDOVASCULAR) - INVIMA Registration 0f87a4a810faa30c0c9b7924612831c6
Access comprehensive regulatory information for ANACONDA (SISTEMA DE INJERTO ENDOVASCULAR) (ANACONDA (ENDOVASCULAR GRAFT SYSTEM)) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 0f87a4a810faa30c0c9b7924612831c6 and manufactured by TERUMO COLOMBIA ANDINA SAS. The device was registered on December 07, 2033.
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 INJERTO ENDOVASCULAR ANACONDA ESTÁ INDICADO PARA LA REPARACIÓN DEL ANEURISMA DE AORTA ABDOMINAL INFRARRENAL (AAA), TAMBIÉN ESTÁ INDICADO PARA LA REPARACIÓN DEL ANEURISMA AISLADO DE LA ARTERIA ILÍACA._x000D_ EL CUELLO AÓRTICO DEL SISTEMA DE INJERTO ENDOVASCULAR ANACONDA ESTÁ INDICADO PARA LOS SIGUIENTES CASOS: USARLO COMO CUELLO DE EXTENSIÓN INFRARRENAL CUANDO EL CUERPO BIFURCADO FIJADO SE HAYA DESPLEGADO DEMASIADO BAJO EN EL CUELLO AÓRTICO Y PARA PROPORCIONAR UN SELLADO ADICIONAL.
THE ANACONDA ENDOVASCULAR GRAFT SYSTEM IS INDICATED FOR THE REPAIR OF THE INFRARENAL ABDOMINAL AORTIC ANEURYSM (AAA), IT IS ALSO INDICATED FOR THE REPAIR OF THE ISOLATED ANEURYSM OF THE ILÍACA._x000D_ ARTERY THE AORTIC NECK OF THE ANACONDA ENDOVASCULAR GRAFT SYSTEM IS INDICATED FOR THE FOLLOWING CASES: USE IT AS AN INFRARED EXTENSION NECK WHEN THE FIXED BIFURCATED BODY HAS BEEN DEPLOYED TOO LOW IN THE AORTIC NECK AND TO PROVIDE ADDITIONAL SEALING.