BEUDAMED
    17 results · 37ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ECLIPSE HUMERAL HEAD EXTRACTOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·December 16, 2024

    ECLIPSE HUMERAL HEAD EXTRACTOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·October 31, 2022

    ECLIPSE HUMERAL HEAD EXTRACTOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·September 8, 2025

    ECLIPSE HUMERAL HEAD EXTRACTOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·November 20, 2024

    ECLIPSE HUMERAL HEAD EXTRACTOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·May 25, 2024

    ECLIPSE HUMERAL HEAD EXTRACTOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·May 15, 2024

    ECLIPSE HUMERAL HEAD EXTRACTOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·November 7, 2024

    ECLIPSE HUMERAL HEAD EXTRACTOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·June 5, 2024

    ECLIPSE HUMERAL HEAD EXTRACTOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·March 12, 2021

    ECLIPSE HUMERAL HEAD EXTRACTOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·March 12, 2021

    ECLIPSE HUMERAL HEAD EXTRACTOR

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code MDM·June 20, 2022

    ALLEGRETTO WAVE EYE-Q

    FDA Adverse Event
    Malfunction ·WAVELIGHT GMBH·Product code LZS·December 22, 2010

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·February 2, 2013

    MINICAP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CLEVELAND·Product code KDI·July 17, 2014

    UNK

    FDA Adverse Event
    Injury ·ARTHREX, INC.·Product code MDM·September 26, 2025

    25MM TAP

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·December 16, 2024

    ECLIPSE RESECT PROTECTOR,SZ L/50.0MM

    FDA Adverse Event
    Malfunction ·ARTHREX, INC.·Product code LXH·December 4, 2023