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

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    Filters Status: Malfunction ×

    UNIVERSAL GLENOID - INLAY LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code PHX·June 21, 2024

    UNIVERSAL GLENOID - INLAY LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code PHX·December 28, 2020

    LIFEPAK(R) 12 DEFIBRILLATOR/MONITOR SERIES

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL, INC·Product code MKJ·January 11, 2013

    PLEURX PLEURAL CATHETER MINI KIT

    FDA Adverse Event
    Malfunction ·CAREFUSION·Product code DWM·July 3, 2014

    UNIVERSAL GLENOID - INLAY LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code PHX·June 20, 2024

    UNIVERSAL GLENOID - INLAY LARGE PLUS

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code PHX·June 20, 2024