BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    OMNIPROBE ELECTRICAL NERVE STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    OPTICAL DVS (DUAL VECTOR SHEARING) ESOPHAGEAL DILATOR

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

    Hammerdesis™ Interphalangeal Fusion System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UNKNOWN RIGHT HIP

    FDA Adverse Event
    Injury ·STRYKER ORTHOPAEDICS MAHWAH·Product code MEH·November 2, 2012

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - SINGAPORE·Product code FKX·May 23, 2014

    DURATA STS OPTIM PASSIVE FIXATION

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 10, 2010

    SURE-T PARADIGM

    FDA Adverse Event
    Malfunction ·UNOMEDICAL A/S·Product code FPA·June 7, 2024