21efcd7413f91659837700e07159c0ed

VIATRAC 14 PLUS PERIPHERAL DILATATION CATHETER / CATÉTER DE DILATACIÓN PERIFÉRICA

ABBOTT LABORATORIES DE COLOMBIA S.A.S.·IIa·Colombia INVIMA·Expires December 22, 2033

Device classification

Risk class / Clase de Riesgo: IIa
Product type (Spanish): MEDICO QUIRURGICOS
Product type (English): SURGICAL DOCTOR

Registration information

Analysis ID: 21efcd7413f91659837700e07159c0ed
Expire date: December 22, 2033

Authorized company / Fabricante

Name (Spanish): ABBOTT LABORATORIES DE COLOMBIA S.A.S.
Name (English): ABBOTT LABORATORIES DE COLOMBIA S.A.S.

Product use / Uso del Producto

Spanish

CATÉTER DE DILATACIÓN DE ESTENOSIS SITUADAS EN ARTERIAS PERIFÉRICAS ILIACA, FEMORAL, POPLITEA, INTRAPOPLITEA, RENAL, LLIOFEMORAL Y PARA EL TRATAMIENTO DE LESIONES OBSTRUCTIVAS DE FÍSTULAS ARTERIOVENOSAS DE HEMODIÁLISIS NATIVAS O SINTÉTICAS.

English

STENOSIS DILATION CATHETER LOCATED IN PERIPHERAL ILIAC, FEMORAL, POPLITEA, INTRAPOPLITEA, RENAL, LLIOFEMORAL ARTERIES AND FOR THE TREATMENT OF OBSTRUCTIVE LESIONS OF NATIVE OR SYNTHETIC HEMODIALYSIS ARTERIOVENOUS FISTULAS.

About this record

Access comprehensive regulatory information for VIATRAC 14 PLUS PERIPHERAL DILATATION CATHETER / CATÉTER DE DILATACIÓN PERIFÉRICA (VIATRAC 14 PLUS PERIPHERAL DILATATION CATHETER / CATÉTER DE DILATACIÓN PERIFÉRICA ) in the Colombia medical device market through Pure Global AI's free database. This IIa medical device is registered under INVIMA analysis ID 21efcd7413f91659837700e07159c0ed and manufactured by ABBOTT LABORATORIES DE COLOMBIA S.A.S.. The device was registered on December 22, 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.