DURADIAGNOST F30 - COFEPRIS Registration 1551E2018 SSA
Access comprehensive regulatory information for DURADIAGNOST F30 (DURADIAGNOST F30) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 1551E2018 SSA and manufactured by PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.. The device was registered on June 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.
EL SISTEMA DURADIAGNOST F30 ESTÁ DISEÑADO LA GENERACIÓN DE IMÁGENES RADIOGRÁFICAS DE LA ANATOMÍA HUMANA. LAS APLICACIONES PUEDEN REALIZARSE CON EL PACIENTE SENTADO, DE PIE O EN DECÚBITO PRONO O SUPINO
THE DURADIAGNOST F30 SYSTEM IS DESIGNED TO GENERATE RADIOGRAPHIC IMAGES OF HUMAN ANATOMY. APPLICATIONS CAN BE PERFORMED WITH THE PATIENT SITTING, STANDING OR IN PRONE OR SUPINE POSITION.