EMBOTRAP TM III / STENT RETRIEVER - DISPOSITIVO DE REVASCULARIZACIÓN - INVIMA Registration fdbc7218d90c02b5449c4c9978e40eca
Access comprehensive regulatory information for EMBOTRAP TM III / STENT RETRIEVER - DISPOSITIVO DE REVASCULARIZACIÓN (EMBOTRAP TM III / STENT RETRIEVER - REVASCULARIZATION DEVICE) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID fdbc7218d90c02b5449c4c9978e40eca and manufactured by JOHNSON & JOHNSON MEDTECH COLOMBIA S.A.S.. The device was registered on December 21, 2031.
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.
LA FINALIDAD DEL DISPOSITIVO DE REVASCULARIZACIÓN EMBOTRAP III ES LA RESTAURACIÓN DE LA CIRCULACIÓN SANGUÍNEA EN PACIENTES QUE SUFREN UN ACCIDENTE CEREBROVASCULAR ISQUÉMICO A CAUSA DE UNA OCLUSIÓN NEUROVASCULAR DE UN VASO DE GRAN TAMAÑO. EL DISPOSITIVO ESTÁ DISEÑADO PARA SU USO EN LA NUEROVASCULATURA ANTERIOR Y POSTERIOR EN VASOS SANGUINEOS, COMO LA ARTERIA CARÓTIDA INTERNA, LOS SEGMENTOS M1 Y M2 DE LA ARTERIA CEREBRAL MEDIA, LOS SEGMENTOS A1 Y A1 DE LA ARTERIA CEREBRAL ANTERIOR, LA ARTERIA BASILAR, LA POSTERIOR CEREBRAL Y LAS ARTERIAS VERTEBRALES._x000D_ EL DISPOSITIVO SOLO DEBE SER UTILIZADO POR MÉDICOS CAPACITADOS PARA REALIZAR CATETERISMOS NEUROINTERVENCIONALES Y PARA EL TRATAMIENTO DE ACCIDENTES CEREBROVASCULARES ISQUEMICOS.
THE PURPOSE OF THE EMBOTRAP III REVASCULARIZATION DEVICE IS TO RESTORE BLOOD CIRCULATION IN PATIENTS WHO SUFFER AN ISCHAEMIC STROKE DUE TO NEUROVASCULAR OCCLUSION OF A LARGE VESSEL. THE DEVICE IS DESIGNED FOR USE IN THE ANTERIOR AND POSTERIOR NUEROVASCULATURE IN BLOOD VESSELS, SUCH AS THE INTERNAL CAROTID ARTERY, THE M1 AND M2 SEGMENTS OF THE MIDDLE CEREBRAL ARTERY, THE A1 AND A1 SEGMENTS OF THE ANTERIOR CEREBRAL ARTERY, THE BASILAR ARTERY, THE POSTERIOR CEREBRAL ARTERY, AND THE ARTERIES VERTEBRALES._x000D_ THE DEVICE SHOULD ONLY BE USED BY PHYSICIANS TRAINED TO PERFORM NEUROINTERVENTIONAL CATHETERIZATIONS AND FOR THE TREATMENT OF ISCHEMIC STROKES.