CAPIOX ARTERIAL FILTER - FILTRO ARTERIAL
- Risk class / Clase de Riesgo
- IIa
- Product type (Spanish)
- MEDICO QUIRURGICOS
- Product type (English)
- SURGICAL DOCTOR
- Analysis ID
- 7cd604fd6942f0a55141559eb477c823
- Expire date
- August 08, 2032
- Name (Spanish)
- TERUMO COLOMBIA ANDINA SAS
- Name (English)
- TERUMO COLOMBIA ANDINA SAS
EL PRODUCTO SE UTILIZA PARA ELIMINAR BURBUJAS DE AIRE Y PARTÍCULAS EXTRAÑAS DEL CIRCUITO ARTERIAL PRINCIPAL DURANTE PROCEDIMIENTOS DE CIRCULACIÓN EXTRACORPÓREA EN UNA CIRUGÍA A CORAZÓN ABIERTO O CIRCULACIÓN ASISTIDA.
THE PRODUCT IS USED TO REMOVE AIR BUBBLES AND FOREIGN PARTICLES FROM THE MAIN ARTERIAL CIRCUIT DURING HEART-LUNG PROCEDURES IN OPEN-HEART SURGERY OR ASSISTED CIRCULATION.
Access comprehensive regulatory information for CAPIOX ARTERIAL FILTER - FILTRO ARTERIAL (CAPIOX ARTERIAL FILTER - FILTRO ARTERIAL) in the Colombia medical device market through Pure Global AI's free database. This IIa medical device is registered under INVIMA analysis ID 7cd604fd6942f0a55141559eb477c823 and manufactured by TERUMO COLOMBIA ANDINA SAS. The device was registered on August 08, 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.