RX ACCULINK CAROTID STENT SYSTEM/ SISTEMA DE STENT CAROTIDEO
- Risk class / Clase de Riesgo
- III
- Product type (Spanish)
- MEDICO QUIRURGICOS
- Product type (English)
- SURGICAL DOCTOR
- Analysis ID
- ef380edbfc1caf11476b854e7ca1b3dd
- Expire date
- March 08, 2034
- Name (Spanish)
- ABBOTT LABORATORIES DE COLOMBIA S.A.S.
- Name (English)
- ABBOTT LABORATORIES DE COLOMBIA S.A.S.
EL SISTEMA DE STENT CAROTÍDEO RX ACCULINK ESTÁ INDICADO PARA USARSE EN PACIENTES CON ATEROESCLEROSIS DE LAS ARTERIAS CARÓTIDAS
THE ACCULINK RX CAROTID STENT SYSTEM IS INDICATED FOR USE IN PATIENTS WITH CAROTID ARTERY ATHEROSCLEROSIS
Access comprehensive regulatory information for RX ACCULINK CAROTID STENT SYSTEM/ SISTEMA DE STENT CAROTIDEO (RX ACCULINK CAROTID STENT SYSTEM/ SISTEMA DE STENT CAROTIDEO) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID ef380edbfc1caf11476b854e7ca1b3dd and manufactured by ABBOTT LABORATORIES DE COLOMBIA S.A.S.. The device was registered on March 08, 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.