DESFIBRILADOR AUTOMÁTICOVISIA AF MRI* SURESCAN* -MEDTRONIC - COFEPRIS Registration 123C2020 SSA
Access comprehensive regulatory information for DESFIBRILADOR AUTOMÁTICOVISIA AF MRI* SURESCAN* -MEDTRONIC (DESFIBRILADOR AUTOMÁTICOVISIA AF MRI* SURESCAN* -MEDTRONIC) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 123C2020 SSA and manufactured by MEDTRONIC, S. DE R.L. DE C.V.. The device was registered on February 10, 2020.
This page provides complete registration details including product type (II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS), 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 VISIA AF MRI SURESCAN ESTÁDISEÑADO PARA PROPORCIONAR UNAESTIMULACIÓN ANTITAQUICARDIAVENTRICULARYDESFIBRILACIÓNVENTRICULARPARA TRATAMIENTOS AUTOMÁTICOS DETAQUIARRITMIASVENTRICULARESQUEPUEDANPONER EN PELIGRO LA VIDA DEL PACIENTE.
THE VISIA AF MRI SURESCAN SYSTEM IS DESIGNED TO PROVIDE ANTITACHYCARDIAENTRICULAR STIMULATION AND VENTRICULAR DEFIBRILLATION FOR AUTOMATIC TREATMENTS OF VENTRICULAR TACHYARRHYTHMIAS, WHICH MAY ENDANGER THE PATIENT'S LIFE.