BEUDAMED
    4 results · 24ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    AUTOSOFT 90

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·July 14, 2024

    SORIN CENTRIFUGAL PUMP 5 (CP5)

    FDA Adverse Event
    Other ·SORIN GROUP DEUTSCHLAND·Product code DTQ·June 27, 2014

    PENUMBRA SYSTEM REPERFUSION CATHETER 054

    FDA Adverse Event
    Injury ·PENUMBRA, INC.·Product code NRY·January 11, 2013

    PHOENIX ANTEGRADE FEMORAL NAIL SYSTEM

    FDA Adverse Event
    Malfunction ·EBI, LLC·Product code HSB·December 2, 2010