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Nombre Clasificación Fabricante Nivel de riesgo País Fuente
Device Recall SynchroMed II implantable drug infusion pump General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall Medtronic SynchroMed EL General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Medtronic SynchroMed II Implantable Infusion Pumps General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Medtronic Synchromed II Implantable Drug Infusion Pump General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Medtronic SynchroMed EL Programable Pump General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Medtronic SynchroMed EL General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Medtronic SynchroMed EL General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall Medtronic SynchroMed II General Hospital and Personal Use Devices Medtronic, Inc. - Neuromodulation 3 United States USFDA
Device Recall SynchroMed EL implantable infusion pump General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall SynchroMed II implantable infusion pump General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall SynchroMed II Implantable Infusion Pump General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall SynchroMed II Implantable Infusion Pump General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall SynchroMed EL Implantable Infusion Pump General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall SynchroMed II Implantable Drug Infusion Pump General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall Medtronic SynchroMed EL General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall Medtronic SynchroMed EL General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall Medtronic SynchroMed II General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall Medtronic SynchroMed EL Programmable Infusion Pump General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall Medtronic SynchroMed EL Programmable Pump General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall Medtronic SynchroMed II Programmable Pump General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall SYNCHROMED II PROGRAMMABLE DRUG INFUSION SYSTEM General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA
Device Recall Medtronic SynchroMed II implantable drug pump General Hospital and Personal Use Devices Medtronic, Inc. - Neuromodulation 3 United States USFDA
Device Recall Medtronic SynchroMed implantable drug pump General Hospital and Personal Use Devices Medtronic, Inc. - Neuromodulation 3 United States USFDA
Device Recall Medtronic SynchroMed EL implantable drug pump General Hospital and Personal Use Devices Medtronic, Inc. - Neuromodulation 3 United States USFDA
SynchroMed II Implantable Drug Infusion System General Hospital and Personal Use Devices Medtronic Neuromodulation 3 United States USFDA