BEUDAMED
    9 results · 23ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Status: Injury ×

    AEQ REV II GLENOID BASEPLATE DIA 25MM

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code PHX·July 1, 2025

    AEQUALIS REVERSED BASE PLATE TA6V LONG PEG WITH HA

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·March 13, 2025

    AEQ REV GLENOID BASEPLATE 29MM

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·March 6, 2025

    GORE EXCLUDER AAA ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·May 22, 2008

    ENDOTAK RELIANCE

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVY·April 12, 2011

    AEQUALIS REVERSED MULTIDIRECTIONAL GLENOID PLATE HA

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·March 25, 2024

    D.4,5MM COMPRESSION SCREW L.32MM

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·January 7, 2025

    D.4,5MM COMPRESSION SCREW L.23MM

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·January 7, 2025

    AEQ REV GLENOID BASEPLATE 29MM

    FDA Adverse Event
    Injury ·TORNIER S.A.S.·Product code KWS·May 21, 2024