BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    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

    ENDOVIVE 3S LOW PROFILE BALLOON KIT

    FDA Adverse Event
    Malfunction ·XERIDIEM MEDICAL DEVICES·Product code PIF·January 11, 2016

    MEGA SUTURECUT NEEDLE DRIVER INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·April 10, 2013

    TENDRIL ST

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code DTB·May 27, 2008

    HEARTSTART MRX - EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS HEALTHCARE·Product code MKJ·April 5, 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