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Name Classification Manufacturer Risk Class Country Source
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
Synchromed II Implantable Drug Infusion Pumps General Hospital and Personal Use Devices Medtronic Germany BAM
the SynchroMed® Implantable Infusion Pump General Hospital and Personal Use Devices Medtronic Germany BAM
the SynchroMed® implantable infusion pump General Hospital and Personal Use Devices Medtronic GmbH Germany BAM
the implantable infusion pump SynchroMed® General Hospital and Personal Use Devices Medtronic Inc. Germany BAM
the Synchromed EL pump motor General Hospital and Personal Use Devices Medtronic Germany BAM
SynchroMed II General Hospital and Personal Use Devices Medtronic Inc. Sweden SMPA
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