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

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    Filters FDA Adverse Event ×

    ZELTIQ COOLCORE (6.3)

    FDA Adverse Event
    Injury ·ZELTIQ AESTHETICS INC.·Product code OOK·February 6, 2013

    NEXGEN CRUCIATE RETAINING FEMORAL COMPONENT

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code JWH·December 7, 2010

    SUMMIT DUOFIX TAP SZ1 STD OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code LPH·July 22, 2014

    1820334-2020-01805

    FDA Adverse Event
    Malfunction ·COOK INC·Product code FOZ·October 5, 2020