APNEALINK RESMED - COFEPRIS Registration 2623E2018 SSA
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.
PARA 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.