MAGNETOM PRISMA - COFEPRIS Registration 134E2018 SSA
Access comprehensive regulatory information for MAGNETOM PRISMA (MAGNETOM PRISMA) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 134E2018 SSA and manufactured by SIEMENS HEALTHCARE DIAGNOSTICS S DE RL DE CV. The device was registered on January 05, 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.
ESTA INDICADO PARA SU USO COMO DISPOSITIVOS PARA RESONANCIA MAGNETICA (DDRM) PRODUCE IMAGENES DE CORTES TRANSVERSALES, SAGITALES, CORONALES Y OBLICUOS E IMAGENES ESPECTROSCOPICAS O 4ESPECTROS Y MUESTRA LA ESTRUCTURA INTERNA O LA FUNCION DE LA CABEZA EL CU
IT IS INDICATED FOR USE AS MAGNETIC RESONANCE DEVICES (DDRM) PRODUCES CROSS-SECTION, SAGITTAL, CORONAL AND OBLIQUE IMAGES AND SPECTROSCOPIC OR 4SPECTRA IMAGES AND SHOWS THE INTERNAL STRUCTURE OR FUNCTION OF THE CU HEAD.