BEUDAMED
    7 results · 27ms · Sources: EU EUDAMED, US FDA

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    TECHTON PROTECTIVE PAD

    FDA 510(k)
    FDA Class 1 ·Radiology

    UCSS® Screw Set

    FDA UDI
    MEDTRONIC SOFAMOR DANEK, INC.·00673978067834·BONE SCREW 873-038 4.0 CANN CORT L 38MM

    CuRAS Nd:YAG Laser

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

    CAREMATIX WELLNESS SYSTEM, MODEL CWS-5000.1-B

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    SMALL BATTERY DRIVE

    FDA Adverse Event
    Malfunction ·NI·Product code HWE·June 13, 2014

    SPECTRA

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FAE·October 14, 2010

    PULSE GEN MODEL 102

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·December 13, 2012