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NC TREK NEO™ CORONARY DILATATION CATHETER / CATÉTER PARA DILATACIÓN CORONARIA - INVIMA Registration 5697659dece81ded9fb2887d08f6d05b

Access comprehensive regulatory information for NC TREK NEO™ CORONARY DILATATION CATHETER / CATÉTER PARA DILATACIÓN CORONARIA (NC TREK NEO™ CORONARY DILATION CATHETER) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID 5697659dece81ded9fb2887d08f6d05b and manufactured by ABBOTT LABORATORIES DE COLOMBIA S.A.S..

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.

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INVIMA Official Data
III
5697659dece81ded9fb2887d08f6d05b
NC TREK NEO™ CORONARY DILATATION CATHETER / CATÉTER PARA DILATACIÓN CORONARIA
INVIMA Analysis ID: 5697659dece81ded9fb2887d08f6d05b
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Product Use / Uso del Producto
Spanish

LOS CATÉTERES DE DILATACIÓN CORONARIA NC TREK NEO™ ESTÁN INDICADOS PARA:_x000D_ A) DILATACIÓN CON BALÓN DE LA PORCIÓN ESTENÓTICA DE UNA ARTERIA CORONARIA O ESTENOSIS DEL BYPASS, CON EL FIN DE MEJORAR LA PERFUSIÓN MIOCÁRDICA_x000D_ B) DILATACIÓN CON BALÓN DE UNA OCLUSIÓN DE ARTERIA CORONARIA, CON EL FIN DE RESTABLECER EL FLUJO CORONARIO EN PACIENTES CON INFARTO DE MIOCARDIO CON ELEVACIÓN DEL SEGMENTO ST_x000D_ C) DILATACIÓN CON BALÓN DE UN STENT DESPUÉS DE LA IMPLANTACIÓN (SOLO MODELOS CON BALÓN DE 2,00 MM - 5,00 MM)_x000D_

English

NC TREK NEO™ CORONARY DILATION CATHETERS ARE INDICATED FOR:_x000D_ A) BALLOON DILATION OF THE STENOTIC PORTION OF A CORONARY ARTERY OR BYPASS STENOSIS, IN ORDER TO IMPROVE PERFUSION MIOCÁRDICA_x000D_ B) BALLOON DILATION OF A CORONARY ARTERY OCCLUSION, IN ORDER TO RESTORE CORONARY FLOW IN PATIENTS WITH MYOCARDIAL INFARCTION WITH ELEVATION OF THE ST_x000D_ SEGMENT C) BALLOON DILATION OF A STENT AFTER IMPLANTATION (ONLY MODELS WITH A 2.00 MM - 5.00 MM BALLOON)_x000D_

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
5697659dece81ded9fb2887d08f6d05b
Authorized Company / Fabricante
Name (English)
ABBOTT LABORATORIES DE COLOMBIA S.A.S.