BEUDAMED
    3 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SURFLASH PLUS SAFETY IV CATHETER

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION - KOFU·Product code FOZ·June 6, 2014

    MULTIFLEX KNOTLESS FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code MBI·November 27, 2012

    CRYSTALENS HD

    FDA Adverse Event
    Malfunction ·BAUSCH & LOMB·Product code NAA·September 29, 2010