BEUDAMED
    5 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    KNEE IMPLANT-TIBIA INSERT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·August 6, 2024

    ULTHERA

    FDA Adverse Event
    Injury ·ULTHERA, INC.·Product code OHV·June 10, 2014

    SETROX S 45

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·December 21, 2012

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·November 3, 2010

    GYC-1000

    FDA Adverse Event
    Malfunction ·NIDEK CO., LTD.·Product code HQF·June 18, 2015