MASCARILLAS SIN VENTILACIÓN (NO VENTILADAS) RESMED
Mexico·Clase II·I. MEDICAL EQUIPMENT·AGUILAR MURGUÍA ASESORES EN SERVICIOS INTEGRALES DE SALUD, S.A. DE C.V.·Registered June 01, 2018LAS 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.
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- MASCARILLAS DE TERAPIA VENTILATORIA
- Trade Name (English)
- VENTILATORY THERAPY MASKS
- Analysis ID
- 1295E2018 SSA
- Registration Date
- June 01, 2018
- Name (English)
- AGUILAR MURGUÍA ASESORES EN SERVICIOS INTEGRALES DE SALUD, S.A. DE C.V.
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.