BEUDAMED
    9 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SINGLE USE DISTAL COVER

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP. HINODE PLANT·Product code FDT·April 20, 2021

    MICROCLAVE

    FDA Adverse Event
    Malfunction ·ICU MEDICAL, INC.·Product code FPA·July 2, 2015

    ASR ACETABULAR IMPLANT 56

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL·Product code KWA·March 26, 2013

    VIRTUOSO VR

    FDA Adverse Event
    Death ·MEDTRONIC MED REL, INC.·Product code LWS·March 16, 2011

    EAGLE 4000

    FDA Adverse Event
    Malfunction ·GE HEALTHCARE·Product code MHX·March 20, 2008

    PINN CAN BONE SCREW 6.5MMX30MM

    FDA Adverse Event
    Injury ·1219655 DEPUY-RAYNHAM·Product code NDJ·October 29, 2014

    PINN CAN BONE SCREW 6.5MMX30MM

    FDA Adverse Event
    Injury ·1219655 DEPUY-RAYNHAM·Product code NDJ·October 29, 2014

    PINNACLE SECTOR II CUP 52MM

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC.·Product code LPH·October 29, 2014

    ZENITH ALPHA THORACIC ENDOVASCULAR GRAFT PROXIMAL TAPERED COMPONENTS

    FDA Adverse Event
    Injury ·WILLIAM COOK EUROPE·Product code MIH·September 12, 2025