BEUDAMED
    8 results · 20ms · Sources: EU EUDAMED, US FDA

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    COBAS E 411 ANALYZER (DISK SYSTEM)

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code JJE·May 27, 2026

    FEMORAL INTRAFIX SCREW & SHEATH SYSTEM, 10MM

    FDA Adverse Event
    Injury ·DEPUY MITEK·Product code MBI·December 7, 2010

    LARGE MOD HEAD ADAPT 12/14 +5

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD. 8010379·Product code KXA·July 9, 2014

    SELF-DRILLING HALF PIN APEX 4MM, 120 X 30MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS SELZACH·Product code JDW·December 14, 2012

    SWAN-GANZ CONTINUOUS CARDIAC CATHETER

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES, PR·Product code KRA·November 11, 2011

    SWAN-GANZ CONTINUOUS CARDIAC CATHETER

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code KRA·November 11, 2011

    SWAN-GANZ CONTINUOUS CARDIAC CATHETER

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES, PR·Product code KRA·November 11, 2011

    SWAN-GANZ CONTINUOUS CARDIAC CATHETER

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES, PR·Product code KRA·November 11, 2011