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RADIFOCUS GLIDEWIRE ADVANTAGE/ CATÉTER GUÍA - INVIMA Registration 6322786bcedf9ae9e03747082169e095

Access comprehensive regulatory information for RADIFOCUS GLIDEWIRE ADVANTAGE/ CATÉTER GUÍA (RADIFOCUS GLIDEWIRE ADVANTAGE/ GUIDE CATHETER) in the Colombia medical device market through Pure Global AI's free database. This IIa medical device is registered under INVIMA analysis ID 6322786bcedf9ae9e03747082169e095 and manufactured by TERUMO COLOMBIA ANDINA SAS. The device was registered on December 13, 2032.

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
IIa
6322786bcedf9ae9e03747082169e095
RADIFOCUS GLIDEWIRE ADVANTAGE/ CATÉTER GUÍA
INVIMA Analysis ID: 6322786bcedf9ae9e03747082169e095
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Product Use / Uso del Producto
Spanish

RADIFOCUS GLIDEWIREADVANTAGE ESTÁ DISEÑADO PARA DIRIGIR UN CATÉTER A LA UBICACIÓN ANATÓMICA DESEADA DURANTE LOS PROCEDIMIENTOS DE DIAGNÓSTICO O INTERVENCIÓN, EXCEPTO PARA EL CORAZÓN O EL SISTEMA CIRCULATORIO CENTRAL.

English

RADIFOCUS GLIDEWIREADVANTAGE IS DESIGNED TO DIRECT A CATHETER TO THE DESIRED ANATOMICAL LOCATION DURING DIAGNOSTIC OR INTERVENTIONAL PROCEDURES, EXCEPT FOR THE HEART OR CENTRAL CIRCULATORY SYSTEM.

Device Classification
Risk Class / Clase de Riesgo
IIa
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
6322786bcedf9ae9e03747082169e095
Expire Date
December 13, 2032
Authorized Company / Fabricante
Name (English)
TERUMO COLOMBIA ANDINA SAS