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

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    Filters FDA Adverse Event ×

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 26, 2013

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 26, 2013

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 26, 2013

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 26, 2013

    HERCULITE ULTRA

    FDA Adverse Event
    Injury ·KERR CORPORATION·Product code EBF·September 26, 2013

    FOLFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·June 5, 2014

    HARMONIC ACE 36CM W ERG HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 4, 2010

    RECEPTAL CANISTER 1000 ML CE

    FDA Adverse Event
    Malfunction ·AMSINO MEDICAL CO., LTD, HOSPIRA INC.·Product code GCX·November 12, 2012