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REBIRTH PRO2 THROMBUS ASPIRATION CATHETER-CATÉTER DE ASPIRACIÓN DE TROMBOS REBIRTH PRO2 - INVIMA Registration a4861ef9e93dd2586a893eb6b8e38382

Access comprehensive regulatory information for REBIRTH PRO2 THROMBUS ASPIRATION CATHETER-CATÉTER DE ASPIRACIÓN DE TROMBOS REBIRTH PRO2 (REBIRTH PRO2 THROMBUS ASPIRATION CATHETER-THROMBUS ASPIRATION CATHETER REBIRTH PRO2) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID a4861ef9e93dd2586a893eb6b8e38382 and manufactured by NIPRO MEDICAL CORPORATION. The device was registered on September 08, 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
a4861ef9e93dd2586a893eb6b8e38382
REBIRTH PRO2 THROMBUS ASPIRATION CATHETER-CATÉTER DE ASPIRACIÓN DE TROMBOS REBIRTH PRO2
INVIMA Analysis ID: a4861ef9e93dd2586a893eb6b8e38382
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Product Use / Uso del Producto
Spanish

CATÉTER INDICADO PARA LA EXTRACCIÓN O DISIPACIÓN PERCUTÁNEA DE TROMBOS DE LA VASCULATURA PERIFÉRICA. PARA ASPIRACIÓN DE TROMBO CORONARIO

English

CATHETER INDICATED FOR THE PERCUTANEOUS EXTRACTION OR DISSIPATION OF THROMBUS FROM THE PERIPHERAL VASCULATURE. FOR CORONARY THROMBUS ASPIRATION

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
a4861ef9e93dd2586a893eb6b8e38382
Expire Date
September 08, 2033
Authorized Company / Fabricante
Name (English)
NIPRO MEDICAL CORPORATION