BEUDAMED
    6 results · 17ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    HYDROCISION ARTHROJET SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIGITAL CLINICAL THERMOMETER MODEL V9XX

    FDA 510(k)
    FDA Class 2 ·General Hospital

    DIGITAL EMG MONITOR MYOTRON 120

    FDA 510(k)
    FDA Class 2 ·Neurology

    GPS STRETCHER

    FDA Adverse Event
    Malfunction ·HILL-ROM INC.·Product code FPO·January 25, 2013

    RADIFOCUS GLIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITIKA·Product code DQX·February 1, 2011

    PARADIGM REAL-TIME REVEL INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 5, 2014