BEUDAMED
    6 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    I-STAT CTNI CARTRIDGE

    FDA Adverse Event
    Malfunction ·ABBOTT POINT OF CARE INC.·Product code MMI·August 5, 2008

    3.5MM/2.5MM DOUBLE DRILL SLEEVE

    FDA Adverse Event
    Malfunction ·SYNTHES USA·Product code FZX·April 29, 2013

    CYPHER SIROLIMUS-ELUTING CORONARY STENT

    FDA Adverse Event
    Injury ·CORDIS LLC (PR)·Product code NIQ·May 9, 2011

    31G PEN NEEDLES

    FDA Adverse Event
    Injury ·BECTON DICKINSON·Product code FMI·July 25, 2008

    VITEK® MS INSTRUMENT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code QBN·September 7, 2022

    VITEK® MS INSTRUMENT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX SA·Product code QBN·September 7, 2022