BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    COULTER GEN-S SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    G.E. MSI 850/850II/1250 THREE PHASE GENERATORS

    FDA 510(k)
    FDA Class 1 ·Radiology

    PreludeSYNC Radial Compression Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 11, 2014

    LIGASURE IMPACT

    FDA Adverse Event
    Malfunction ·COVIDIEN LP·Product code GEI·January 23, 2013

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP., MEDICAL DIV.·Product code FNL·December 22, 2010

    INFUSOMAT SPACE PUMP IV SET

    FDA Adverse Event
    Malfunction ·B. BRAUN DOMINICAN REPUBLIC·Product code FPA·November 17, 2009