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

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    Filters FDA Adverse Event ×

    DXTEND HIGHMO PE CUP D38 +3MM

    FDA Adverse Event
    Injury ·DEPUY FRANCE SAS REG. # 3003895575·Product code KWS·May 20, 2014

    ASR ACETABULAR CUPS 54

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·November 6, 2012

    ULTRACISION HARMONIC SCALPEL HAND PIECE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC. (CINCINNATI)·Product code LFL·September 20, 2007