BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    ACU-CURETTE

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

    N.A.

    FDA UDI
    DENTAURUM GmbH & Co.KG·J011891334000·10 cases Topic Roth 18 Brackets / For further i...

    MULTISCOPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    Tek RMD (TEK ROBOTIC MOBILIZATION DEVICE) TEKRMD02, TEKRMD03, TEKRMD04, TEKRMD04, TEKRMD05, TEKRMD06, TEKRMD07, TEKRMD08

    FDA 510(k)
    FDA Class 2 ·Physical Medicine

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 31, 2014

    ADVANTA BED

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·November 2, 2010

    GREENLIGHT HPS LASER SYSTEM

    FDA Adverse Event
    Malfunction ·AMERICAN MEDICAL SYSTEMS·Product code GEX·December 21, 2012