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

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    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 25, 2014

    NAVISTAR DIAGNOSTIC/ ABLATION CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER, INC (IRWINDALE)·Product code DRF·November 8, 2010

    UNKNOWN REJUVENATE NECK

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code LZO·December 21, 2012