MASCARILLAS SIN VENTILACIÓN (NO VENTILADAS) RESMED - COFEPRIS Registration 1295E2018 SSA
Access comprehensive regulatory information for MASCARILLAS SIN VENTILACIÓN (NO VENTILADAS) RESMED (UNVENTILATED (NON-VENTILATED) MASKS RESMED) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1295E2018 SSA and manufactured by AGUILAR MURGUÍA ASESORES EN SERVICIOS INTEGRALES DE SALUD, S.A. DE C.V.. The device was registered on June 01, 2018.
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.
LAS MASCARILLAS SIN VENTILACIÓN (NO VENTILADAS) RESMED DEBEN SER UTILIZADAS POR PACIENTES ADULTOS (> 30 KG/ 66LB) QUE REQUIEREN ASISTENCIA VENTILATORIA QUE NO SEA DE APOYO VITAL. PARA SU USO EN EL HOGAR O EN ENTORNOS HOSPITALARIOS/INSTITUCIONES.
RESMED UNVENTILATED (NON-VENTILATED) MASKS SHOULD BE USED BY ADULT PATIENTS (> 30 KG/ 66LB) WHO REQUIRE NON-LIFE-SUSTAINING VENTILATORY SUPPORT. FOR USE AT HOME OR IN HOSPITAL/INSTITUTIONAL SETTINGS.