BEUDAMED
    3 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    KINETRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code MHY·June 10, 2014

    VENTAK PRIZM 2

    FDA Adverse Event
    Malfunction ·GUIDANT CLONMEL IRELAND·Product code LWS·October 11, 2010

    UNKNOWN DEPUY ASR FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KXA·December 10, 2012