BEUDAMED
    8 results · 16ms · Sources: EU EUDAMED, US FDA

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    FEMRX MORCELLATOR SYSTEM

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    GYNECARE X-TRACT MORCELLATOR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code HET·June 16, 2006

    TAMPER HAMPER

    FDA 510(k)
    FDA Unclassified ·Unknown

    KINESIA

    FDA 510(k)
    FDA Class 2 ·Neurology

    SCREW,FIXATION,BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HWC·July 11, 2016

    GOBED II

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL-KALAMAZOO·Product code FNL·February 15, 2013

    RENEW RECEIVER

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION DIVISION·Product code GZB·December 22, 2010

    8CM ANGLE ATTACHMENT

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES POWER TOOLS, 4500 RIVERSIDE DR.·Product code HBC·December 13, 2013