PRODIVA 1.5T - COFEPRIS Registration 2734E2018 SSA
Access comprehensive regulatory information for PRODIVA 1.5T (PRODIVA 1.5T) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 2734E2018 SSA and manufactured by PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.. The device was registered on December 10, 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.
PRODIVA 1.5T ES UN SISTEMA ELECTROMÉDICO DE RESONANCIA MAGNÉTICA INDICADO PARA USO COMO EQUIPO DE DIAGNÓSTICO QUE PUEDE GENERAR IMÁGENES TRANSVERSALES Y ESPECTROSCÓPICAS EN CUALQUIER ORIENTACIÓN DE LA ESTRUCTURA INTERNA DE LA CABEZA, EL CUERPO O LAS EXTRE
PRODIVA 1.5T IS AN ELECTROMEDICAL MAGNETIC RESONANCE SYSTEM INDICATED FOR USE AS DIAGNOSTIC EQUIPMENT THAT CAN GENERATE CROSS-SECTIONAL AND SPECTROSCOPIC IMAGES IN ANY ORIENTATION OF THE INTERNAL STRUCTURE OF THE HEAD, BODY OR EXTREMITIES.