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

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    SOMNOPLASTY SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ACUSON AcuNav Volume Intracardiac Echocardiography Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VERIFY SIRIUS BIOLOGICAL INDICATOR CHALLENGE PACK

    FDA 510(k)
    FDA Class 2 ·General Hospital

    LUMAX 540 DR-T

    FDA Adverse Event
    Death ·BIOTRONIK SE & CO. KG·Product code MRM·February 13, 2013

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 19, 2011

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·August 1, 2014

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·October 2, 2024