MARCAPASOS CONDICIONAL MRI CON TECNOLOGÍA SURESCAN*-MEDTRONIC
Mexico·Clase III·II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS·MEDTRONIC, S. DE R.L. DE C.V.·Registered June 27, 2019LOS SISTEMAS MRI SURESCAN ESTÁN INDICADOS PARA PACIENTES QUE PUEDEN BENEFICIARSE DE ESTIMULACIÓN CON O SIN RESPUESTA DE FRECUENCIA PARA RESTABLECER LAS FRECUENCIAS CARDÍACAS FISIOLÓGICAS, MEJORAR EL GASTO CARDÍACO, PREVENIR SÍNTOMAS O PROTEGER CONTRA ARRI
SURESCAN MRI SYSTEMS ARE INDICATED FOR PATIENTS WHO MAY BENEFIT FROM STIMULATION WITH OR WITHOUT FREQUENCY RESPONSE TO RESTORE PHYSIOLOGICAL HEART RATES, IMPROVE CARDIAC OUTPUT, PREVENT SYMPTOMS, OR PROTECT AGAINST AR.
- Risk Class / Clase de Riesgo
- Clase III
- Product Type (Spanish)
- II. PROTESIS, ÓRTESIS Y AYUDAS FUNCIONALES
- Product Type (English)
- II. PROSTHETICS, ORTHOSES AND FUNCTIONAL AIDS
- Trade Name (Spanish)
- GENERADOR DE PULSO IMPLANTABLE
- Trade Name (English)
- IMPLANTABLE PULSE GENERATOR
- Analysis ID
- 1243C2019 SSA
- Registration Date
- June 27, 2019
- Name (Spanish)
- MEDTRONIC, S. DE R.L. DE C.V.
- Name (English)
- MEDTRONIC, S. DE R.L. DE C.V.
Access comprehensive regulatory information for MARCAPASOS CONDICIONAL MRI CON TECNOLOGÍA SURESCAN*-MEDTRONIC (MRI CONDITIONAL PACEMAKER WITH SURESCAN*-MEDTRONIC TECHNOLOGY) in the Mexico medical device market through Pure Global AI's free database. This Clase III medical device is registered under COFEPRIS analysis ID 1243C2019 SSA and manufactured by MEDTRONIC, S. DE R.L. DE C.V.. The device was registered on June 27, 2019.
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.