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NERVE MONITORING SYSTEM AND ACCESSORIES-SISTEMA DE MONITORIZACIÓN NERVIOSA Y ACCESORIOS - INVIMA Registration 5060af6c66f2661ad18db9013bc4b4ec

Access comprehensive regulatory information for NERVE MONITORING SYSTEM AND ACCESSORIES-SISTEMA DE MONITORIZACIÓN NERVIOSA Y ACCESORIOS (NERVE MONITORING SYSTEM AND ACCESSORIES) in the Colombia medical device market through Pure Global AI's free database. This IIa medical device is registered under INVIMA analysis ID 5060af6c66f2661ad18db9013bc4b4ec and manufactured by MEDTRONIC INC. The device was registered on December 06, 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
IIa
5060af6c66f2661ad18db9013bc4b4ec
NERVE MONITORING SYSTEM AND ACCESSORIES-SISTEMA DE MONITORIZACIÓN NERVIOSA Y ACCESORIOS
INVIMA Analysis ID: 5060af6c66f2661ad18db9013bc4b4ec
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Product Use / Uso del Producto
Spanish

EL TUBO ENDOTRAQUEAL DE EMG ESTÁ DISEÑADO TANTO PARA PROPORCIONAR AL PACIENTE UNA VÍA DE VENTILACIÓN ABIERTA COMO PARA LA MONITORIZACIÓN INTRAOPERATORIA DE LA ACTIVIDAD EMG DE LA MUSCULATURA LARÍNGEA CUANDO SE CONECTA A UN MONITOR EMG ADECUADO. EL USO DEL TUBO DE EMG ESTÁ INDICADO CUANDO SE REQUIERE MONITORIZAR CONTINUAMENTE LOS NERVIOS QUE CONDUCEN LOS IMPULSOS HASTA LA MUSCULATURA LARÍNGEA DURANTE LAS INTERVENCIONES QUIRÚRGICAS.

English

THE EMG ENDOTRACHEAL TUBE IS DESIGNED BOTH TO PROVIDE THE PATIENT WITH AN OPEN VENTILATION LINE AND FOR INTRAOPERATIVE MONITORING OF EMG ACTIVITY OF THE LARYNGEAL MUSCULATURE WHEN CONNECTED TO AN APPROPRIATE EMG MONITOR. THE USE OF THE EMG TUBE IS INDICATED WHEN IT IS NECESSARY TO CONTINUOUSLY MONITOR THE NERVES THAT CONDUCT THE IMPULSES TO THE LARYNGEAL MUSCULATURE DURING SURGICAL INTERVENTIONS.

Device Classification
Risk Class / Clase de Riesgo
IIa
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
5060af6c66f2661ad18db9013bc4b4ec
Expire Date
December 06, 2033
Authorized Company / Fabricante
Name (Spanish)
MEDTRONIC INC
Name (English)
MEDTRONIC INC