BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DUROM ACETABULAR COMPONENT

    FDA Adverse Event
    Other ·ZIMMER GMBH·Product code KWA·May 27, 2014

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·January 11, 2013

    KARL STORZ DEBAKEY

    FDA Adverse Event
    Malfunction ·KARL STORZ·Product code GCJ·November 19, 2010

    "1.5MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·April 2, 2019

    "1.5MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·April 10, 2019

    "1.5MM" SYSTEM HIGH TORQUE (HT) CROSS-DRIVE SCREW

    FDA Adverse Event
    Injury ·BIOMET MICROFIXATION·Product code JEY·August 3, 2018

    PRODISC-L TRIAL-IMPL L 9° 10

    FDA Adverse Event
    Malfunction ·OBERDORF SYNTHES PRODUKTIONS GMBH·Product code MJO·January 15, 2019

    VITEK® 2 AST-GP75 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX, INC·Product code LON·February 12, 2018