BEUDAMED
    15 results · 65ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ZIMMER® PATIENT SPECIFIC INSTRUMENT

    FDA Adverse Event
    Injury ·MATERIALISE USA, LLC·Product code JWH·September 11, 2015

    SURGICASE

    FDA Adverse Event
    Injury ·MATERIALISE USA, LLC·Product code PBF·April 15, 2021

    TRUMATCH

    FDA Adverse Event
    Malfunction ·MATERIALISE USA LLC·Product code JEY·April 27, 2022

    MATERIALISE PERSONALIZED SOLUTION

    FDA Adverse Event
    Injury ·MATERIALISE USA, LLC·Product code PBF·May 22, 2024

    SURGICASE

    FDA Adverse Event
    Injury ·MATERIALISE USA, LLC·Product code PBF·June 2, 2022

    TRUMATCH CMF

    FDA Adverse Event
    Injury ·MATERIALISE USA, LLC.·Product code JEY·July 9, 2025

    TRUMATCH

    FDA Adverse Event
    Injury ·MATERIALISE USA, LLC·Product code HWT·July 6, 2022

    TRUMATCH

    FDA Adverse Event
    Injury ·MATERIALISE USA, LLC·Product code HWT·August 30, 2021

    TRUMATCH

    FDA Adverse Event
    Injury ·MATERIALISE USA, LLC·Product code JEY·December 7, 2023

    TRUMATCH

    FDA Adverse Event
    Injury ·MATERIALISE USA, LLC·Product code JEY·December 21, 2023

    PROPLAN CMF

    FDA Adverse Event
    Malfunction ·MATERIALISE USA LLC·Product code JEY·December 21, 2023

    TRUMATCH

    FDA Adverse Event
    Injury ·MATERIALISE USA, LLC·Product code JEY·February 6, 2025

    TRUMATCH

    FDA Adverse Event
    Injury ·MATERIALISE USA, LLC·Product code JEY·January 10, 2025

    ZIMMER PATIENT SPECIFIC INSTRUMENT

    FDA Adverse Event
    Injury ·MATERIALISE USA LLC.·Product code HSX·May 5, 2015

    SURGICASE

    FDA Adverse Event
    Injury ·MATERIALISE USA, LLC·Product code PBF·November 22, 2019