BEUDAMED
    6 results · 21ms · Sources: EU EUDAMED, US FDA

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    ANNULAR ARRAY PROBES FOR ARTIS 3200 DIAG. ULTRA.

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Change Healthcare Enterprise Viewer

    FDA 510(k)
    FDA Class 2 ·Radiology

    MOBLVAC W.C.

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

    DURATA STS OPTIM ACTIVE FIXATION, DF4 CONNECTOR

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL INC., CARDIAC RHYTHM MANAGEMENT D·Product code NVY·January 13, 2014

    TERUMO PERFUSION SYSTEM 8000

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP·Product code JOR·October 1, 2010

    LIFEVEST WCD 4000 SYSTEM

    FDA Adverse Event
    Malfunction ·ZOLL LIFECOR CORPORATION·Product code MVK·November 16, 2012