BEUDAMED
    14 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    UNIVERSAL GLENOID - INLAY LARGE

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

    UNIVERSAL GLENOID - INLAY LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·April 30, 2019

    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

    FREESTYLE FREEDOM

    FDA Adverse Event
    Injury ·Product code NBW·December 1, 2010

    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

    UNI GLENOID-PERIPHERAL LOCK SCRW

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·July 26, 2024

    ECLIPSE TRUNION,45 MM TPS CTD

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·July 26, 2024

    CENTRAL SCREW, NL, UNI REV, 6.5X25MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code KWS·July 26, 2024

    ECLIPSE CAGE SCREW XL, 45MM

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code QHQ·July 26, 2024

    UNIVERSAL GLENOID - INLAY LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·July 26, 2024

    UNIVERSAL GLENOID - BASEPLATE LARGE

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code PHX·July 26, 2024