BEUDAMED
    3 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    LINOX SMART S 60

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVY·June 13, 2014

    TELIGEN

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWP·October 16, 2010

    UNKNOWN LEFT HIP REJUVENATE/ ABGII NECK

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MEH·December 6, 2012