VENUE - COFEPRIS Registration 517E2018 SSA
Access comprehensive regulatory information for VENUE (VENUE) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 517E2018 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 ULTRASONIDO VENUE ESTÁ DISEÑADO PARA LA OBTENCIÓN DE IMÁGENES POR ULTRASONIDO, MEDICIÓN Y ANÁLISIS DEL CUERPO HUMANO Y SUS FLUIDOS EN MÚLTIPLES APLICACIONES CLÍNICAS, QUE INCLUYEN APLICACIONES ABDOMINALES (GINECOLOGÍA Y UROLOGÍA), TORÁCICAS
THE VENUE ULTRASOUND SYSTEM IS DESIGNED FOR ULTRASOUND IMAGING, MEASUREMENT AND ANALYSIS OF THE HUMAN BODY AND ITS FLUIDS IN MULTIPLE CLINICAL APPLICATIONS, INCLUDING ABDOMINAL (GYNECOLOGY AND UROLOGY), THORACIC APPLICATIONS.