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

    Oticon

    FDA UDI
    Oticon A/S·05714464008018·AGXO F400 MINIRITE R C091

    A8, A9 Anesthesia System

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    QUARTEX Occipito-Cervico-Thoracic Spinal System, Globus Navigation Instruments

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·November 3, 2014

    SM304 M-SERIES W/ZOOM

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code INK·August 17, 2011

    HEARTSTART MRX -EMS DEFIBRILLATOR

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·July 3, 2013