BEUDAMED
    7 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·May 30, 2014

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC.·Product code DRM·October 23, 2012

    HEART START XL

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·September 16, 2010

    MAGNUM HEAD

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWA·March 8, 2018

    UNKNOWN STEM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 8, 2018

    E-POLY LINER

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 8, 2018

    CRUZ RT TRIFLANGE

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code JDI·March 8, 2018