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FINESTREAM S PLUS PTA BALLON DILATATION CATHETER CATÉTER DE DILATACIÓN CON BALÓN FINESTREAM S PLUS PTA - INVIMA Registration a13a3980e70d09ac0943ecb9da1a71c1

Access comprehensive regulatory information for FINESTREAM S PLUS PTA BALLON DILATATION CATHETER CATÉTER DE DILATACIÓN CON BALÓN FINESTREAM S PLUS PTA (FINESTREAM S PLUS PTA BALLON DILATATION CATHETER BALLOON DILATION CATHETER FINESTREAM S PLUS PTA) in the Colombia medical device market through Pure Global AI's free database. This III medical device is registered under INVIMA analysis ID a13a3980e70d09ac0943ecb9da1a71c1 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
a13a3980e70d09ac0943ecb9da1a71c1
FINESTREAM S PLUS PTA BALLON DILATATION CATHETER CATÉTER DE DILATACIÓN CON BALÓN FINESTREAM S PLUS PTA
INVIMA Analysis ID: a13a3980e70d09ac0943ecb9da1a71c1
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Product Use / Uso del Producto
Spanish

DISPOSITIVO ESTÁ DISEÑADO PARA LA DILATACIÓN DE VASOS ESTENÓTICOS (ARTERIAS, VENAS O DERIVACIONES) DURANTE LA ANGIOPLASTIA TRASLUMINAL PERCUTÁNEA (ATP) O LA DILATACIÓN POSTERIOR A LA COLOCACIÓN DE STENTS.

English

THE DEVICE IS DESIGNED FOR DILATION OF STENOTIC VESSELS (ARTERIES, VEINS, OR SHUNTS) DURING PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (ATP) OR DILATION FOLLOWING STENTING.

Device Classification
Risk Class / Clase de Riesgo
III
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
a13a3980e70d09ac0943ecb9da1a71c1
Expire Date
September 08, 2033
Authorized Company / Fabricante
Name (English)
NIPRO MEDICAL CORPORATION