BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    1832415-2017-08675

    FDA Adverse Event
    Injury ·October 9, 2018

    1832415-2018-09738

    FDA Adverse Event
    Malfunction ·October 28, 2018

    1832415-2018-09678

    FDA Adverse Event
    Malfunction ·October 4, 2018

    1832415-2017-09097

    FDA Adverse Event
    Malfunction ·April 5, 2018

    2008K HEMODIALYSIS SYS OLC/DIASAFE PLUS

    FDA Adverse Event
    Malfunction ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KDI·March 27, 2014

    ION¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code NIQ·November 14, 2012

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code MDS·September 13, 2010

    LIFEPAK CR(R) PLUS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·December 21, 2017