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

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    Filters Status: Malfunction ×

    HEMOCHRON SIGNATURE ELITE

    FDA Adverse Event
    Malfunction ·ACCRIVA DIAGNOSTICS·Product code JPA·May 25, 2016

    LIFEPAK 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC.·Product code MKJ·December 8, 2010

    CAUTERY UNIT

    FDA Adverse Event
    Malfunction ·PENTAX MEDICAL CO.·Product code GEI·October 17, 2006