BEUDAMED
    10 results · 22ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    F&P Optiflow Filtered Nasal Interface with Anesthesia Mask Compatibility (AA041J)

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    M.U.S.T. PEDICLE SCREWS SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025

    Beamer AVEO Electrosurgical Generator, Beamer AVEO Argon Module, Beamer AVEO Cart, Beamer AVEO Wired Foot Pedal, Beamer AVEO Argon Pressure Reducer

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

    SPHERICAL TIP CORONARY OSTIAL CANNULA, MODEL 30011

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    M.U.S.T. PEDICLE SCREW SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·January 13, 2026

    M.U.S.T. PEDICLE SCREWS SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code NKB·November 10, 2025

    TAXUS LIBERTE' PACLITAXEL-ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC·Product code NIQ·November 4, 2008

    MODEL NOT SPECIFIED

    FDA Adverse Event
    Injury ·MEDTRONIC MINIMED·Product code LZG·August 29, 2011

    PROLENE POLYPROPYLENE MESH UNKNOWN PRODUCT

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTL·July 18, 2013

    M.U.S.T. SACRAL ILIAC SCREW AND PELVIC TRAUMA SYSTEM

    FDA Adverse Event
    Malfunction ·MEDACTA INTERNATIONAL SA·Product code OUR·October 16, 2024