INTUIS - COFEPRIS Registration 90E2018 SSA
Access comprehensive regulatory information for INTUIS (INTUIS) in the Mexico medical device market through Pure Global AI's free database. This Clase II medical device is registered under COFEPRIS analysis ID 90E2018 SSA and manufactured by PHILIPS MÉXICO COMMERCIAL, S.A. DE C.V.. The device was registered on January 04, 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 EQUIPO INTUIS DE PHILIPS ES UN SISTEMA DE RAYOS X MONOPLANO PARA PROCEDIMIENTOS QUIRÚRGICOS Y DE DIAGNÓSTICO CARDIOVASCULARES
PHILIPS INTUIS EQUIPMENT IS A MONOPLANE X-RAY SYSTEM FOR CARDIOVASCULAR DIAGNOSTIC AND SURGICAL PROCEDURES