BEUDAMED
    13 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ERBE

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code GEI·November 2, 2022

    AXSYM DIGOXIN III

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS INTERNATIONAL, LTD.·Product code KXT·May 11, 2007

    ADVIA CENTAUR VANCOMYCIN (VANC) ASSAY

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code LEH·March 19, 2013

    ESPRIT VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC.·Product code CBK·March 8, 2011

    DISCOVERY XS HUMERAL 3.5X84MM RT FLANGE

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDC·December 14, 2012

    MO.MA

    FDA Adverse Event
    Death ·INVATEC SPA·Product code NTE·August 28, 2014

    MO.MA

    FDA Adverse Event
    Injury ·INVATEC SPA·Product code NTE·August 28, 2014

    MO.MA

    FDA Adverse Event
    Injury ·INVATEC SPA·Product code NTE·August 28, 2014

    ERBE

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code GEI·March 8, 2023

    ERBE

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code GEI·February 18, 2025

    ERBE

    FDA Adverse Event
    Injury ·LEONHARD LANG GMBH·Product code GEI·July 27, 2022

    DISCOVERY ELBOW XS HUMERAL CONDYLE KIT - HEXALOBULAR

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDC·July 17, 2012

    DISCOVERY ELBOW XS HUMERAL CONDYLE KIT - HEXALOBULAR

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code JDC·July 17, 2012