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

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    DRI-LYTE

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    Diode laser hair removal device

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

    LTM-T SURGICAL MESH

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

    CENTRA

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FNL·May 7, 2010

    EON MINI

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·October 5, 2012

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FRN·December 3, 2013

    130 DEG AIMING ARM F/TROCHANTERIC FIXATION NAILS

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code FZX·May 29, 2014

    BUTTRESS/COMPRESSION NUT FOR 357.369

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code HST·May 29, 2014

    HELICAL BLADE COUPLING SCREW

    FDA Adverse Event
    Malfunction ·SYNTHES BRANDYWINE·Product code LXH·May 29, 2014