BEUDAMED
    6 results · 27ms · Sources: EU EUDAMED, US FDA

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    KLIP-LITE

    FDA 510(k)
    FDA Class 1 ·Dental

    INERTIA PEDICLE SCREW SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Infrared Forehead Thermometer

    FDA 510(k)
    FDA Class 2 ·General Hospital

    REVIVE - THROMBECTOMY DEVICE

    FDA Adverse Event
    Injury ·MICRUS ENDOVASCULAR, LLC·Product code DXE·May 5, 2014

    CAPSUREFIX

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code DTB·October 15, 2012

    CAPSURE SENSE

    FDA Adverse Event
    Malfunction ·MEDTRONIC, INC.·Product code DTB·August 10, 2010