BEUDAMED
    4 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PENUMBRA SYSTEM REPERFUSION CATHETER 041

    FDA Adverse Event
    Malfunction ·PENUMBRA INC.·Product code NRY·November 18, 2010

    HEARTMATE II LVAD

    FDA Adverse Event
    Death ·THORATEC CORPORATION·Product code DSQ·January 24, 2013

    MINICAP TRANSFER SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·July 11, 2014

    PRLNE BLU 24IN 8-0 D/A BV130-5 EP

    FDA Adverse Event
    Malfunction ·ETHICON INC.·Product code GAW·November 29, 2023