INNOSIGHT - COFEPRIS Registration 643E2018 SSA
Access comprehensive regulatory information for INNOSIGHT (INNOSIGHT) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 643E2018 SSA and manufactured by PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.. The device was registered on March 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.
EL SISTEMA DE ULTRASONIDO DE DIAGNÓSTICO INNOSIGHT ESTÁ DISEÑADO PARA LA GENERACIÓN DE IMÁGENES POR ULTRASONIDO DIAGNÓSTICO EN LOS MODOS SIGUIENTES: B (2D), MODO M, DOPPLER PW, CPA, IMÁGENES ARMÓNICAS TISULARES Y DOPPLER COLOR. ESTÁ INDICADO PARA LA GENER
THE INNOSIGHT DIAGNOSTIC ULTRASOUND SYSTEM IS DESIGNED FOR DIAGNOSTIC ULTRASOUND IMAGING IN THE FOLLOWING MODES: B (2D), M MODE, PW DOPPLER, CPA, TISSUE HARMONIC IMAGING, AND COLOR DOPPLER. IT IS INDICATED FOR THE GENER