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CATETE DE ASPIRACIÓN ELIMINATE / CATETER - INVIMA Registration a69dd138616a2259b81d4bca9f57b599

Access comprehensive regulatory information for CATETE DE ASPIRACIÓN ELIMINATE / CATETER (ELIMINATE ASPIRATION CATHETE / CATHETER ) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID a69dd138616a2259b81d4bca9f57b599 and manufactured by TERUMO COLOMBIA ANDINA SAS. The device was registered on May 04, 2033.

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
a69dd138616a2259b81d4bca9f57b599
CATETE DE ASPIRACIÓN ELIMINATE / CATETER
INVIMA Analysis ID: a69dd138616a2259b81d4bca9f57b599
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Product Use / Uso del Producto
Spanish

EL CATETER ELIMINATE ESTÁ DESTINADO A LA ELIMINACIÓN DE ÉMBOLOS Y TROMBOS FRESCOS Y BLANDOS DE LOS VASOS DE LA VASCULATURA CORONARIA Y PERIFÉRICA.

English

THE ELIMINATE CATHETER IS INTENDED FOR THE REMOVAL OF FRESH, SOFT EMBOLI AND THROMBI FROM THE VESSELS OF THE CORONARY AND PERIPHERAL VASCULATURE.

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
a69dd138616a2259b81d4bca9f57b599
Expire Date
May 04, 2033
Authorized Company / Fabricante
Name (English)
TERUMO COLOMBIA ANDINA SAS