BEUDAMED
    4 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    PLATE MUELLER HINTON II AGAR

    FDA Adverse Event
    Malfunction ·BECTON, DICKINSON & CO. (SPARKS)·Product code JTZ·October 26, 2022

    ALUMINA HEAD

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code MRA·December 4, 2008

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·September 9, 2011

    1.85MM TI MATRIX SCREW SELF-DRILLING/5MM

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code JEY·July 29, 2013