BEUDAMED
    4 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DUROM ACETAULAR COPONENT

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWA·May 20, 2014

    IMPAX CV REPORTING

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·November 12, 2012

    TRIDENT PSL HA SOLID BACK 52MM

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS CORK·Product code MEH·September 20, 2010

    T25 STARDRIVE SHAFT F/MATRIX LONG

    FDA Adverse Event
    Malfunction ·SYNTHES GMBH·Product code HXX·April 25, 2023