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

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    Filters FDA Adverse Event ×

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·May 30, 2014

    INFUSE BONE GRAFT

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK USA, INC·Product code NEK·November 20, 2012

    DEPO-PROVERA¿ INJECTABLE SUSPENSION

    FDA Adverse Event
    Malfunction ·TEVA PHARMACEUTICAL INDUSTRIES·Product code FMF·September 3, 2010