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

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    COLONOSCOPE GUIDING TUBE DEVICE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SCALPEL, ONE-PIECE, DISPOSABLE

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    PACESETTER SYSTEMS, INC. ENDOCARDIAL SCREW-IN LEAD

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    UNKNOWN DEPUY DURALOC ACETABULAR LINER

    FDA Adverse Event
    Injury ·DEPUY ORTHOPAEDICS, INC. 1818910·Product code KWA·June 19, 2014

    NC QUANTUM APEX PTCA DILATATION CATHETER

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code LOX·October 28, 2010

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·December 3, 2012