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RESUCITADOR INFANTIL BABYPUFF 1020 - INVIMA Registration 784e82c65e6ce81e0176fdca77c96ede

Access comprehensive regulatory information for RESUCITADOR INFANTIL BABYPUFF 1020 (INFANT RESUSCITATOR BABYPUFF 1020) in the Colombia medical device market through Pure Global AI's free database. This IIa medical device is registered under INVIMA analysis ID 784e82c65e6ce81e0176fdca77c96ede and manufactured by LM INSTRUMENTS S.A.. The device was registered on October 19, 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.

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INVIMA Official Data
IIa
784e82c65e6ce81e0176fdca77c96ede
RESUCITADOR INFANTIL BABYPUFF 1020
INVIMA Analysis ID: 784e82c65e6ce81e0176fdca77c96ede
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Product Use / Uso del Producto
Spanish

EL RESUCITADOR INFANTIL BABYPUFF MODELO 1020 FACILITA LA ENTREGA DE PIP CONTROLADA Y SEGURA AL PACIENTE PARA LLENAR DE AIRE/O2 SUS PULMONES Y ALCANZAR REFUERZO ALVEOLAR MรXIMO SIN DILATACIร“N EN EXCESO. SUMINISTRA, TAMBIร‰N PEEP CONSISTENTE PARA AYUDAR A ESTABLECER Y MANTENER LA CAPACIDAD RESIDUAL FUNCIONAL (FRC), PROPORCIONANDO UN รNDICE RESPIRATORIO IDEAL PARA UN MEJOR CAMBIO GASEOSO.

English

THE BABYPUFF MODEL 1020 INFANT RESUSCITATOR FACILITATES THE DELIVERY OF CONTROLLED AND SAFE PIP TO THE PATIENT TO FILL THEIR LUNGS WITH AIR/O2 AND ACHIEVE MAXIMUM ALVEOLAR REINFORCEMENT WITHOUT EXCESSIVE DILATION. IT ALSO SUPPLIES CONSISTENT PEEP TO HELP ESTABLISH AND MAINTAIN FUNCTIONAL RESIDUAL CAPACITY (FRC), PROVIDING AN IDEAL RESPIRATORY INDEX FOR BETTER GAS CHANGE.

Device Classification
Risk Class / Clase de Riesgo
IIa
Product Type (Spanish)
MEDICO QUIRURGICOS
Product Type (English)
SURGICAL DOCTOR
Registration Information
Analysis ID
784e82c65e6ce81e0176fdca77c96ede
Expire Date
October 19, 2031
Authorized Company / Fabricante
Name (Spanish)
LM INSTRUMENTS S.A.
Name (English)
LM INSTRUMENTS S.A.