BEUDAMED
    11 results · 18ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    UNIDENTIFIED ASR HEAD

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KXA·July 6, 2015

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·January 2, 2013

    LOCKING SCREW, TITANIUM 3.5MM X 22MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    LO-PRO SCRW,TI,3.5MMX 26MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    LO-PRO SCRW,TI,3.5MMX 38MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    LO-PRO SCRW,TI,3.5MMX 30MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    CALCANEAL FRAC PERIMETER PLT,XS,RT

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HRS·April 18, 2019

    LO-PRO SCRW,TI,3.5MMX 24MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    LO-PRO SCRW,TI,3.5MMX 34MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    LO-PRO SCRW,TI,3.5MMX 36MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019

    LOCKING SCREW, TITANIUM 3.5MM X 28MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code HWC·April 18, 2019