MOBILEDIAGNOST M50 - COFEPRIS Registration 529E2018 SSA
Access comprehensive regulatory information for MOBILEDIAGNOST M50 (MOBILEDIAGNOST M50) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 529E2018 SSA and manufactured by PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.. The device was registered on February 23, 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.
EL DISPOSITIVO MOBILEDIAGNOST M50 ES UN SISTEMA RADIOGRÁFICO MÓVIL QUE SE USA PARA OBTENER IMÁGENES RADIOGRÁFICAS GENERALES. EL SISTEMA MOBILEDIAGNOST M50 ES APTO PARA TODOS LOS TIPOS DE EXÁMENES RADIOGRÁFICOS RUTINARIOS EN ÁREAS DIFÍCILES COMO CUIDADOS I
THE MOBILEDIAGNOST M50 IS A MOBILE RADIOGRAPHIC SYSTEM USED TO OBTAIN GENERAL RADIOGRAPHIC IMAGES. THE MOBILEDIAGNOST M50 SYSTEM IS SUITABLE FOR ALL TYPES OF ROUTINE RADIOGRAPHIC EXAMINATIONS IN DIFFICULT AREAS SUCH AS CARE AND