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

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    Filters FDA Adverse Event ×

    K042172

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code FPA·September 2, 2022

    ONQ PAIN RELIEF SYSTEM

    FDA Adverse Event
    Malfunction ·I-FLOW·Product code MEB·April 1, 2013

    JOSTENT GRAFTMASTER

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MAF·April 5, 2011

    XACT CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·ABBOTT VASCULAR GALWAY·Product code NIM·May 8, 2008