SIGNA ARTIST - COFEPRIS Registration 521E2018 SSA
Access comprehensive regulatory information for SIGNA ARTIST (SIGNA ARTIST) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 521E2018 SSA and manufactured by GE SISTEMAS MÉDICOS DE MÉXICO, S.A. DE C.V.. The device was registered on February 22, 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 DE RESONANCIA MAGNÉTICA (RM) SIGNA ARTIST ESTÁ INDICADO PARA USARSE COMO EQUIPO DE OBTENCIÓN DE IMÁGENES DE DIAGNÓSTICO Y GENERAR IMÁGENES AXIALES, SAGITALES, CORONALES Y OBLICUAS, IMÁGENES ESPECTROSCÓPICAS, MAPAS PARAMÉTRICOS O DE ESPECTRO E I
THE SIGNA ARTIST MAGNETIC RESONANCE IMAGING (MRI) SYSTEM IS INDICATED FOR USE AS DIAGNOSTIC IMAGING EQUIPMENT TO GENERATE AXIAL, SAGITTAL, CORONAL AND OBLIQUE IMAGES, SPECTROSCOPIC IMAGING, PARAMETRIC OR SPECTRUM MAPS AND