BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    KODAK ORTHO G FILM

    FDA 510(k)
    FDA Class 1 ·Radiology

    uDR 592h, uDR 596i

    FDA 510(k)
    FDA Class 2 ·Radiology

    BONE MARROW BIOPSY DEVICE

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

    SOFPORT SQUARE EDGE LENS

    FDA Adverse Event
    Injury ·BAUSCH + LOMB·Product code HQL·October 12, 2012

    6800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 10, 2014

    REVEAL DX

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DSI·August 10, 2010