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RX ACCULINK CAROTID STENT SYSTEM/ SISTEMA DE STENT CAROTIDEO - INVIMA Registration ef380edbfc1caf11476b854e7ca1b3dd

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.

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INVIMA Official Data
III
ef380edbfc1caf11476b854e7ca1b3dd
RX ACCULINK CAROTID STENT SYSTEM/ SISTEMA DE STENT CAROTIDEO
INVIMA Analysis ID: ef380edbfc1caf11476b854e7ca1b3dd
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Product Use / Uso del Producto
Spanish

EL SISTEMA DE STENT CAROTรDEO RX ACCULINK ESTร INDICADO PARA USARSE EN PACIENTES CON ATEROESCLEROSIS DE LAS ARTERIAS CARร“TIDAS

English

THE ACCULINK RX CAROTID STENT SYSTEM IS INDICATED FOR USE IN PATIENTS WITH CAROTID ARTERY ATHEROSCLEROSIS

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
ef380edbfc1caf11476b854e7ca1b3dd
Expire Date
March 08, 2034
Authorized Company / Fabricante
Name (English)
ABBOTT LABORATORIES DE COLOMBIA S.A.S.