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

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    Filters Status: Injury ×

    ASPHERE M SPEC 12/14 36 +1.5

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·January 22, 2013

    XIENCE XPEDITION EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·July 9, 2014

    LATERAL STRAIGHT STEM 15.0 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWB·March 28, 2012

    SULOX-HD 32 M 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·April 23, 2019

    SULOX, HEAD, M¸ 32/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWB·August 3, 2018

    5.0MM TI SCHANZ SCREW BLUNTED TROCAR POINT 200MM

    FDA Adverse Event
    Injury ·SYNTHES RARON·Product code HWC·December 29, 2016

    5.0MM TI SCHANZ SCREW BLUNTED TROCAR POINT 150MM

    FDA Adverse Event
    Injury ·SYNTHES RARON·Product code HWC·December 29, 2016

    5.0MM TI SCHANZ SCREW BLUNTED TROCAR POINT 200MM

    FDA Adverse Event
    Injury ·SYNTHES RARON·Product code HWC·December 29, 2016

    5.0MM TI SCHANZ SCREW BLUNTED TROCAR POINT 150MM

    FDA Adverse Event
    Injury ·SYNTHES RARON·Product code HWC·December 29, 2016

    SULOX-HEAD 28 M 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LPH·April 4, 2019