BEUDAMED
    6 results · 16ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    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

    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