BEUDAMED
    8 results · 28ms · Sources: EU EUDAMED, US FDA

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    ReNew XR Handpiece, 25cm, with Reference Markings (3943M); ReNew XR Handpiece, 34cm, with Reference Markings (3941M); ReNew XR Handpiece, 42cm, with Reference Markings (3942M); ReNew XR Handpiece, Ratcheted, 25cm, with Reference Markings (3946M); ReNew XR Handpiece, Ratcheted, 34cm, with Reference Markings (3944M); ReNew XR Handpiece, Ratcheted, 42cm, with Reference Markings (3945M)

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

    Oticon

    FDA UDI
    Sbo Hearing A/S·05714464034758·OTICON MORE 1 MINIBTE T C092

    Double Internal Joint Stabilizer- Elbow

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Hammerdesis™ Interphalangeal Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    M300

    FDA Adverse Event
    Death ·DRAEGER MEDICAL SYSTEMS, INC. (IT/M)·Product code MHX·August 30, 2011

    FLO-GARD 6201 VOLUMETRIC INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE (SG)·Product code FRN·November 19, 2008

    XENFORM

    FDA Adverse Event
    Other ·TEI BIOSCIENCES INC.·Product code FTM·July 16, 2013

    ONE TOUCH ULTRA2 METER

    FDA Adverse Event
    Injury ·LIFESCAN, INC.·Product code NBW·May 19, 2010