SENOGRAPHE CRYSTAL NOVA - COFEPRIS Registration 208E2018 SSA
Access comprehensive regulatory information for SENOGRAPHE CRYSTAL NOVA (SENOGRAPHE CRYSTAL NOVA) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 208E2018 SSA and manufactured by GE SISTEMAS MÉDICOS DE MÉXICO, S.A. DE C.V.. The device was registered on January 18, 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 SENOGRAPHE CRYSTAL NOVA ESTÁ INDICADO PARA GENERAR IMÁGENES MAMOGRÁFICAS DIGITALES QUE PERMITEN DETECTAR Y DIAGNOSTICAR LESIONES DE MAMA. HA SIDO DISEÑADO PARA REALIZAR EXÁMENES DE DESPISTAJE Y EXPLORACIONES DE DIAGNÓSTICO, INCLUYENDO IMÁGENES
THE SENOGRAPHE CRYSTAL NOVA SYSTEM IS INDICATED TO GENERATE DIGITAL MAMMOGRAPHIC IMAGES THAT ALLOW TO DETECT AND DIAGNOSE BREAST LESIONS. HAS BEEN DESIGNED TO PERFORM SCREENING EXAMINATIONS AND DIAGNOSTIC SCANS, INCLUDING IMAGING