BEUDAMED
    5 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·May 8, 2014

    UNKNOWN ZIMMER KNEE

    FDA Adverse Event
    Injury ·ZIMMER, INC.·Product code JWH·October 18, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·September 7, 2007

    DRILL

    FDA Adverse Event
    Malfunction ·MEDTRONIC (1-800-962-9888)·Product code HBE·March 30, 2016

    ENDO CATCH II 15 MM

    FDA Adverse Event
    Injury ·COVIDEN (DISTRIBUTED BY CARDINAL HEALTH 1-800-964-5227) 1-800-962-9888·Product code GCI·August 12, 2015