BEUDAMED
    3 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    E SERIES DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORP·Product code MKJ·February 4, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 11, 2007

    3.5MM LOCKING SCREW SLF-TPING W/STARDRIVE RECESS 14MM

    FDA Adverse Event
    Injury ·SYNTHES, INC.·Product code KTT·October 18, 2012