BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    LM ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756024426·Stockinette

    LUMENIS ONE FAMILY OF SYSTEMS; LUMENIS ONE.

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

    ARTLINE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 9, 2014

    T.W. POWER SUPPLY

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC.·Product code HQO·January 25, 2013

    RENEW SINGLE RECEIVER

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL - NEUROMODULATION DIV.·Product code LGW·December 16, 2010