BEUDAMED
    6 results · 62ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    QUICKIE QM710

    FDA Adverse Event
    Injury ·SUNRISE MEDICAL (US) LLC·Product code ITI·April 3, 2018

    MEERA EU WITHOUT AUTO DRIVE

    FDA Adverse Event
    Malfunction ·HOLGER ULLRICH·Product code FQO·February 22, 2019

    DEKA SMARTXIDE2

    FDA Adverse Event
    Injury ·EL.EN. ELECTRONIC ENGINEERING S.P.A.·Product code GEX·November 3, 2023

    DJO STIMULATOR

    FDA Adverse Event
    Injury ·DJO LLC·Product code LOF·March 22, 2013

    ALPHAMAXX (460 MM LONGIT. SHIFT), EU

    FDA Adverse Event
    Malfunction ·HOLGER ULLRICH·Product code FQO·February 15, 2018

    CAPNOSTAT C5

    FDA Adverse Event
    Malfunction ·RESPIRONICS NOVAMETRIX, LLC·Product code CCK·December 5, 2019