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

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    PROGRAMALITH III MODELS 238 & 239

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    BIOTIS ANAEROBIC KBE AGAR

    FDA 510(k)
    FDA Class 1 ·Microbiology

    JAKOBI SURG. INSTRUMENTS #11 11/13/14

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    VIKING M

    FDA Adverse Event
    Malfunction ·LIKO AB·Product code FSA·June 3, 2014

    POWER PORT

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code LJT·November 8, 2012

    TERUMO CDI 500 BLOOD PARAMETER MONITOR

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code DRY·September 3, 2010