BEUDAMED
    9 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    DRILL BIT, 1.7MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code HTW·August 12, 2024

    DRIVER SHAFT, T8, SELF RETAINING, AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·August 2, 2024

    DRIVER SHAFT, T8, SELF RETAINING, AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·December 8, 2025

    DRIVER SHAFT, T8, SELF RETAINING, AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·June 4, 2024

    DRIVER SHAFT, T8, SELF RETAINING, AO

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·February 5, 2025

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·April 28, 2014

    VITALITY

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 15, 2010

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code OYC·December 12, 2012

    CARPENTIER-EDWARDS SUPRAANNULAR BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·April 24, 2020