G30E / G40E. - COFEPRIS Registration 526E2019 SSA
Access comprehensive regulatory information for G30E / G40E. (G30E / G40E.) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 526E2019 SSA and manufactured by PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.. The device was registered on March 14, 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.
LOS MONITORES DE PACIENTE G30E Y G40E ESTÁN DESTINADOS AL USO POR PARTE DE PROFESIONALES SANITARIOS EN TODOS AQUELLOS CASOS DONDE SEA NECESARIO MONITORIZAR LOS PARÁMETROS FISIOLÓGICOS DE PACIENTES. LOS MONITORES DE PACIENTE G30E Y G40E SE UTILIZAN PARA MO
THE G30E AND G40E PATIENT MONITORS ARE INTENDED FOR USE BY HEALTHCARE PROFESSIONALS IN ALL CASES WHERE IT IS NECESSARY TO MONITOR THE PHYSIOLOGICAL PARAMETERS OF PATIENTS. G30E AND G40E PATIENT MONITORS ARE USED FOR MO