1039de0d8bb3b013b99c6f5f83220cc0

CÁNULA GUEDEL

GUEDEL CANULA

MEDITEC S.A.·I·Colombia INVIMA·Expires June 04, 2031

Device classification

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

Registration information

Analysis ID: 1039de0d8bb3b013b99c6f5f83220cc0
Expire date: June 04, 2031

Authorized company / Fabricante

Name (Spanish): MEDITEC S.A.
Name (English): MEDITEC S.A.

Product use / Uso del Producto

Spanish

LA CÁNULA GUEDE MANTIENE LA VÍA AÉREA PERMEABLE INTRODUCIÉNDOLA POR LA BOCA. SE UTILIZA PARA LA ADMINISTRACIÓN DE OXÍGENO Y GASES ANESTÉSICOS A LOS PACIENTES, TAMBIÉN ES USADO PARA EVITAR QUE LOS PACIENTES SE LASTIMEN LA LENGUA CUANDO DESPIERTEN DESPUÉS DE LA OPERACIÓN CON ANESTESIA GENERAL. _x000D_ _x000D_ _x000D_

English

THE GUEDE CANNULA KEEPS THE AIRWAY PERMEABLE BY INSERTING IT THROUGH THE MOUTH. IT IS USED FOR THE ADMINISTRATION OF OXYGEN AND ANESTHETIC GASES TO PATIENTS, IT IS ALSO USED TO PREVENT PATIENTS FROM INJURING THEIR TONGUE WHEN THEY WAKE UP AFTER THE OPERATION UNDER GENERAL ANESTHESIA. _x000D_ _x000D_ _x000D_

About this record

Access comprehensive regulatory information for CÁNULA GUEDEL (GUEDEL CANULA) in the Colombia medical device market through Pure Global AI's free database. This I medical device is registered under INVIMA analysis ID 1039de0d8bb3b013b99c6f5f83220cc0 and manufactured by MEDITEC S.A.. The device was registered on June 04, 2031.

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.