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CAPIOX ICP CENTRIFUGAL PUMP 3CX*CP8 / BOMBA CENTRIFUGA - INVIMA Registration 12af0361b971b86acdbab41bc54224f7

Access comprehensive regulatory information for CAPIOX ICP CENTRIFUGAL PUMP 3CX*CP8 / BOMBA CENTRIFUGA (CAPIOX ICP CENTRIFUGAL PUMP 3CX*CP8 / BOMBA CENTRIFUGA) in the Colombia medical device market through Pure Global AI's free database. This IIa medical device is registered under INVIMA analysis ID 12af0361b971b86acdbab41bc54224f7 and manufactured by TERUMO COLOMBIA ANDINA SAS. The device was registered on February 27, 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
IIa
12af0361b971b86acdbab41bc54224f7
CAPIOX ICP CENTRIFUGAL PUMP 3CX*CP8 / BOMBA CENTRIFUGA
INVIMA Analysis ID: 12af0361b971b86acdbab41bc54224f7
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Product Use / Uso del Producto
Spanish

LA BOMBA CENTRรFUGA CAPIOX ICP ES UN DISPOSITIVO ESTร‰RIL DE UN SOLO USO QUE SE UTILIZA COMO BOMBA DE SANGRE EXTRACORPร“REA EN PROCEDIMIENTOS DE BYPASS CARDIOPULMONAR.

English

THE CAPIOX ICP CENTRIFUGAL PUMP IS A STERILE, SINGLE-USE DEVICE USED AS AN EXTRACORPOREAL BLOOD PUMP IN CARDIOPULMONARY BYPASS PROCEDURES.

Device Classification
Risk Class / Clase de Riesgo
IIa
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
12af0361b971b86acdbab41bc54224f7
Expire Date
February 27, 2033
Authorized Company / Fabricante
Name (English)
TERUMO COLOMBIA ANDINA SAS