BEUDAMED
    8 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    GLENOID INSERTER/IMPACTOR, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·August 1, 2025

    GLENOID INSERTER/IMPACTOR, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·December 6, 2024

    GLENOID INSERTER/IMPACTOR, LARGE

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·August 20, 2025

    CAPSUREFIX NOVUS

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·December 14, 2010

    INFUSOR

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·January 22, 2013

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL, INC., CRMD·Product code NVN·July 9, 2014

    ANGLED REAMER, DRIVE SHAFT

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·November 17, 2023

    ANGLED REAMER SLEEVE, 10°

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·November 17, 2023