BEUDAMED
    8 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DELTA CER HEAD 12/14 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code LZO·October 30, 2012

    DELTA CER HEAD 12/14 36MM +1.5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code LZO·October 30, 2012

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·October 30, 2012

    UNKNOWN DEPUY FEMORAL HEAD

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD. ¿ REG. # 8010379·Product code KWY·June 25, 2014

    HUDSON/MODIFIED TRINKLE ATTACH

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS KALAMAZOO·Product code KIJ·November 5, 2010

    LIBERTY CYCLER SET, DUAL PATIENT CONNECT

    FDA Adverse Event
    Malfunction ·REYNOSA MFG·Product code FKX·December 27, 2012

    SUMMIT POR TAPER SZ6 HI OFF

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.1818910·Product code LPH·April 9, 2015

    PINNACLE MTL INS NEUT36IDX52OD

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·October 30, 2012