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

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    Filters FDA Adverse Event ×

    ARCHITECT C8000 SYSTEM

    FDA Adverse Event
    Malfunction ·ABBOTT MANUFACTURING INC·Product code JJE·April 18, 2014

    BD 33G LANCET

    FDA Adverse Event
    Injury ·BD·Product code FMK·May 1, 2014

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·October 1, 2007

    COLLAR

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code NKB·October 24, 2012