BEUDAMED
    7 results · 21ms · Sources: EU EUDAMED, US FDA

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    E. CAM PROFILE ATTENUATION CORRECTION

    FDA 510(k)
    FDA Class 2 ·Radiology

    PEG GUIDEWIRE SYSTEM GASTROSTOMY TUBE KIT

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

    EXETER OPERATING LOUPE

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    EQUINOXE CAGE GLENOID L, POST AUG, LEFT

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code KWS·January 8, 2024

    HEARTSTART FRX

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·May 5, 2014

    IMPLANTABLE NEUROSTIMULATOR

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code MHY·February 15, 2013

    TRANSTAR STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FPO·January 12, 2011