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CÁNULA NASOFARÍNGEA SILICONIZADA - INVIMA Registration beebb1b33cd1a49e5022d9edba00cdf3

Access comprehensive regulatory information for CÁNULA NASOFARÍNGEA SILICONIZADA (SILICONIZED NASOPHARYNGEAL CANNULA) in the Colombia medical device market through Pure Global AI's free database. This IIa medical device is registered under INVIMA analysis ID beebb1b33cd1a49e5022d9edba00cdf3 and manufactured by LM INSTRUMENTS S.A.. The device was registered on June 06, 2032.

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
beebb1b33cd1a49e5022d9edba00cdf3
CÁNULA NASOFARÍNGEA SILICONIZADA
INVIMA Analysis ID: beebb1b33cd1a49e5022d9edba00cdf3
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Product Use / Uso del Producto
Spanish

EL DISPOSITIVO ESTÁ DISEÑADO PARA INSERTARSE EN EL ÁREA NASOFARÍNGEA A TRAVÉS DE LA FOSA NASAL PARA MANTENER ABIERTAS LAS VÍAS RESPIRATORIAS._x000D_

English

THE DEVICE IS DESIGNED TO BE INSERTED INTO THE NASOPHARYNGEAL AREA THROUGH THE NOSTRIL TO KEEP THE PATHWAYS OPEN RESPIRATORIAS._x000D_

Device Classification
Risk Class / Clase de Riesgo
IIa
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
beebb1b33cd1a49e5022d9edba00cdf3
Expire Date
June 06, 2032
Authorized Company / Fabricante
Name (Spanish)
LM INSTRUMENTS S.A.
Name (English)
LM INSTRUMENTS S.A.