BEUDAMED
    6 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    K083526

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC.·Product code CBK·May 7, 2018

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS, INC·Product code CBK·July 20, 2021

    ANTEROLAT DIST TIB PLT, SS, RIGHT, 16H

    FDA Adverse Event
    Injury ·ARTHREX INC.·Product code HRS·June 14, 2018

    ACCU-CHEK ® AVIVA COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code NBW·June 19, 2014

    PURELIGHT

    FDA Adverse Event
    Malfunction ·NONIN MEDICAL, INC·Product code DQA·October 19, 2010

    SWAN-GANZ BIPOLAR PACING CATHETER FOR FEMORAL INSERTION

    FDA Adverse Event
    Malfunction ·EDWARDS LIFESCIENCES, PR·Product code LDF·December 21, 2012