APNEALINK RESMED
Mexico·Clase II·I. MEDICAL EQUIPMENT·AGUILAR MURGUÍA ASESORES EN SERVICIOS INTEGRALES DE SALUD, S.A. DE C.V.·Registered November 14, 2018PARA EL DIAGNÓSTICO DE TRASTORNOS RESPIRATORIOS DEL SUEÑO EN PACIENTES ADULTOS. PARA SU USO EN ENTORNOS DOMICILIARIOS Y HOSPITALARIOS BAJO LAS INDICACIONES DE UN PROFESIONAL DE LA SALUD.
FOR THE DIAGNOSIS OF SLEEP-DISORDERED BREATHING IN ADULT PATIENTS. FOR USE IN HOME AND HOSPITAL SETTINGS UNDER THE DIRECTION OF A HEALTHCARE PROFESSIONAL.
- Risk Class / Clase de Riesgo
- Clase II
- Product Type (Spanish)
- I. EQUIPO MÉDICO
- Product Type (English)
- I. MEDICAL EQUIPMENT
- Trade Name (Spanish)
- EQUIPO PARA EL DIAGNÓSTICO DE TRASTORNOS RESPIRATORIOS DURANTE EL SUEÑO.
- Trade Name (English)
- EQUIPMENT FOR THE DIAGNOSIS OF BREATHING DISORDERS DURING SLEEP.
- Analysis ID
- 2623E2018 SSA
- Registration Date
- November 14, 2018
- Name (English)
- AGUILAR MURGUÍA ASESORES EN SERVICIOS INTEGRALES DE SALUD, S.A. DE C.V.
Access comprehensive regulatory information for APNEALINK RESMED (APNEALINK 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 2623E2018 SSA and manufactured by AGUILAR MURGUÍA ASESORES EN SERVICIOS INTEGRALES DE SALUD, S.A. DE C.V.. The device was registered on November 14, 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.