BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    DIACAM (510(K) K 901019)

    FDA Adverse Event
    Other ·SIEMENS MEDICAL SYSTEMS·Product code KPS·March 13, 2001

    FLOGARD

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FRN·June 30, 2014

    MP20 INTELLIVUE PATIENT MONITOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MHX·November 12, 2010

    TOTALCARE SPO2RT

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·November 30, 2012

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·October 5, 2015

    ULTRACISION HARMONIC ACE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·November 9, 2015

    HARMONIC ACE 36CM W ERG HANDLE

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code LFL·January 30, 2018