BEUDAMED
    11 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    REVIVER VIEW AED

    FDA Adverse Event
    Injury ·DEFIBTECH, LLC·Product code MKJ·April 11, 2014

    LIFELINE AED

    FDA Adverse Event
    Injury ·DEFIBTECH, LLC·Product code MKJ·June 6, 2014

    REVIVER AED

    FDA Adverse Event
    Injury ·DEFIBTECH, LLC·Product code MKJ·May 1, 2012

    LIFELINE, AED

    FDA Adverse Event
    Injury ·DEFIBTECH, LLC·Product code MKJ·December 5, 2008

    REVIVER AED

    FDA Adverse Event
    Injury ·DEFIBTECH, LLC·Product code MKJ·August 2, 2011

    LIFELINE AED

    FDA Adverse Event
    Injury ·DEFIBTECH, LLC·Product code MKJ·December 18, 2012

    LIFELINE AED

    FDA Adverse Event
    Injury ·DEFIBTECH, LLC·Product code MKJ·March 16, 2009

    DEFIBTECH AUTOMATIC COMPRESSION DEVICE

    FDA Adverse Event
    Injury ·DEFIBTECH, LLC.·Product code DRM·April 22, 2026

    REVIVER VIEW AED

    FDA Adverse Event
    Injury ·DEFIBTECH, LLC·Product code MKJ·January 23, 2015

    LIFELINE AED

    FDA Adverse Event
    Injury ·DEFIBTECH, LLC·Product code MKJ·March 13, 2015

    DEFIBTECH LIFELINE ARM ACC

    FDA Adverse Event
    Injury ·DEFIBTECH LLC.·Product code DRM·November 21, 2023