BEUDAMED
    8 results · 58ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    THUVERA 200UM SINGLE USE FLAT TIP FIBER

    FDA Adverse Event
    Malfunction ·IPG MEDICAL CORPORATION·Product code GEX·November 21, 2025

    EON IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Other ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code GZB·November 21, 2007

    EON IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Other ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·November 9, 2007

    ANS QUATTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Other ·ADVANCED NEUROMODULATION SYSTEMS, INC·Product code LGW·August 6, 2007

    ANS QUATTRODE PERCUTANEOUS LEAD

    FDA Adverse Event
    Other ·ADVANCED NEUROMODULATION SYSTEMS, INC·Product code LGW·August 6, 2007

    EON IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Other ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·January 4, 2007

    ANS OCTRODE LEAD

    FDA Adverse Event
    Other ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code GZB·January 4, 2007

    AVISTA MRI

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·November 5, 2020