FINESTREAM S PLUS PTA BALLON DILATATION CATHETER CATÉTER DE DILATACIÓN CON BALÓN FINESTREAM S PLUS PTA
- Risk class / Clase de Riesgo
- III
- Product type (Spanish)
- MEDICO QUIRURGICOS
- Product type (English)
- SURGICAL DOCTOR
- Analysis ID
- a13a3980e70d09ac0943ecb9da1a71c1
- Expire date
- September 08, 2033
- Name (Spanish)
- NIPRO MEDICAL CORPORATION
- Name (English)
- NIPRO MEDICAL CORPORATION
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.
THE DEVICE IS DESIGNED FOR DILATION OF STENOTIC VESSELS (ARTERIES, VEINS, OR SHUNTS) DURING PERCUTANEOUS TRANSLUMINAL ANGIOPLASTY (ATP) OR DILATION FOLLOWING STENTING.
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.