CONCENTRADOR DE OXÍGENO DEVILBISS® - COFEPRIS Registration 1651E2019 SSA
Access comprehensive regulatory information for CONCENTRADOR DE OXÍGENO DEVILBISS® (DEVILBISS® OXYGEN CONCENTRATOR) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1651E2019 SSA and manufactured by AGUILAR MURGUÍA ASESORES EN SERVICIOS INTEGRALES DE SALUD, S.A. DE C.V.. The device was registered on August 16, 2019.
This page provides complete registration details including product type (I. MEDICAL EQUIPMENT), manufacturer information, and regulatory compliance data from the official Mexico COFEPRIS medical device database. Pure Global AI offers free access to Mexico's complete medical device registry with bilingual Spanish/English support, helping global MedTech companies navigate COFEPRIS regulations efficiently.
EL CONCENTRADOR DE OXÍGENO DEVILBISS® ESTÁ DESTINADO A PROPORCIONAR UNA TERAPIA SUPLEMENTARIA DE OXÍGENO DE BAJO FLUJO PARA PACIENTES QUE PADECEN EPOC, ALGUNA ENFERMEDAD CARDIOVASCULAR Y TRASTORNOS PULMONARES. EL CONCENTRADOR DEVILBISS® SE PUEDE UTILIZAR
THE DEVILBISS® OXYGEN CONCENTRATOR IS INTENDED TO PROVIDE SUPPLEMENTAL LOW-FLOW OXYGEN THERAPY FOR PATIENTS SUFFERING FROM COPD, CARDIOVASCULAR DISEASE AND LUNG DISORDERS. THE DEVILBISS® HUB CAN BE USED