BEUDAMED
    10 results · 17ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·April 25, 2023

    MAESTRO FOOT SWITCH

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 6, 2018

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·November 3, 2023

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code OAD·September 7, 2023

    AFX

    FDA Adverse Event
    Malfunction ·ENDOLOGIX, INC.·Product code MIH·January 22, 2016

    MAESTRO 4000 POD, 100W

    FDA Adverse Event
    Malfunction ·STELLARTECH RESEARCH CORPORATION·Product code LPB·August 17, 2023

    MAESTRO 4000 CONTROLLER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC CORPORATION·Product code LPB·October 2, 2023

    INRATIO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·March 9, 2011

    3I T3® NON-PLATFORM SWITCHED TAPERED IMPLANT 5 X 10MM

    FDA Adverse Event
    Malfunction ·BIOMET 3I·Product code DZE·March 12, 2018

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LGW·October 8, 2019