TRITON FAMILY PERIPHERAL BALLON CATHETERES - CATÉTERES DE BALÓN PERIFÉRICO - RONTIS - INVIMA Registration 539c6a116d603da024b1bed82bb45027
Access comprehensive regulatory information for TRITON FAMILY PERIPHERAL BALLON CATHETERES - CATÉTERES DE BALÓN PERIFÉRICO - RONTIS (TRITON FAMILY PERIPHERAL BALLON CATHETERS - PERIPHERAL BALLOON CATHETERS - RONTIS ) in the Colombia medical device market through Pure Global AI's free database. This IIa medical device is registered under INVIMA analysis ID 539c6a116d603da024b1bed82bb45027 and manufactured by NIPRO MEDICAL CORPORATION. The device was registered on September 13, 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.
LA FAMILIA TRITON (CATÉTER BALÓN PERIFÉRICO) ESTÁ DESTINADA A SER UTILIZADAS EN EL TRATAMIENTO DE PACIENTES CON VASOS OBSTRUIDOS ARTERIOESCLERÓTICOS RELACIONADOS CON LA CONDICIÓN PATOLÓGICA DE UNA O MÁS ARTERIAS PERIFÉRICAS.
THE TRITON FAMILY (PERIPHERAL BALLOON CATHETER) IS INTENDED TO BE USED IN THE TREATMENT OF PATIENTS WITH ARTERIOSCLEROTIC OBSTRUCTED VESSELS RELATED TO THE PATHOLOGICAL CONDITION OF ONE OR MORE PERIPHERAL ARTERIES.