EFFICIA DFM100 - COFEPRIS Registration 2205E2019 SSA
Access comprehensive regulatory information for EFFICIA DFM100 (EFFICIA DFM100) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 2205E2019 SSA and manufactured by PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.. The device was registered on December 04, 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.
EFFICIA DFM100 ESTÁ INDICADO PARA SU USO EN ENTORNOS HOSPITALARIOS O EN SERVICIOS DE EMERGENCIAS POR PARTE DE PERSONAL MÉDICO CUALIFICADO FORMADO EN EL USO DEL EQUIPO Y CUALIFICADO MEDIANTE ENTRENAMIENTO EN SOPORTE VITAL BÁSICO, SOPORTE VITAL AVANZADO O D
EFFICIA DFM100 IS INDICATED FOR USE IN HOSPITAL SETTINGS OR EMERGENCY SERVICES BY QUALIFIED MEDICAL PERSONNEL TRAINED IN THE USE OF THE EQUIPMENT AND QUALIFIED BY TRAINING IN BASIC LIFE SUPPORT, ADVANCED LIFE SUPPORT OR