BEUDAMED
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    Filters FDA Adverse Event ×

    COULTER® ACT DIFF 2 ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER INC·Product code GKZ·December 7, 2010

    ASR UNI FEMORAL IMPL SIZE 43

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·February 8, 2013

    THORATEC VENTRICULAR ASSIST DEVICE (VAD) SYSTEM

    FDA Adverse Event
    Injury ·THORATEC CORP.·Product code DSQ·July 11, 2014

    ENDOTAK RELIANCE

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code NVY·January 6, 2011