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

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    ROOT CANAL LENGTH MEASURING DEVICE

    FDA 510(k)
    FDA Unclassified ·Unknown

    TriVerse X-Ray Digital Template, Tibial 80 MM Keel

    FDA UDI
    SIGNATURE ORTHOPAEDICS PTY LTD·09348215114435·

    T2 - NAIL HOLDING SCREW, TIBIA 10 MM

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code LXH·May 21, 2025

    T2 - NAIL HOLDING SCREW, TIBIA 10 MM

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code LXH·June 23, 2025

    FiberLocker Implant ; FiberLocker Instrument ; FiberLocker PowerUnit

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

    PANTEX DIRECT DHEA-S COATED TUBE RADIOIMMUNOASSAY

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Injury ·INSULET CORPORATION·Product code LZG·February 1, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 15, 2010

    PERMANENT CAUTERY SPATULA INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·July 23, 2014

    T2 - NAIL HANDLE

    FDA Adverse Event
    Malfunction ·STRYKER GMBH·Product code LXH·May 21, 2025