BEUDAMED
    6 results · 27ms · Sources: EU EUDAMED, US FDA

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    3-DAY BIOINDICATOR RELEASE FOR RESPIR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    KLASSIC HD HIP SYSTEM, OFFSET FEMORAL STEM, NON-POROUS / POROUS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SYNGO PERFUSION-CT

    FDA 510(k)
    FDA Class 2 ·Radiology

    IMPAX CV DICOMSTORE WITH MEDIA PURGE DAEMON (MPD)

    FDA Adverse Event
    Malfunction ·AGFA HEALTHCARE CORP.·Product code LLZ·May 27, 2014

    PROMUS ELEMENT ¿

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - GALWAY·Product code NIQ·November 15, 2012

    FREESTYLE LITE

    FDA Adverse Event
    Malfunction ·Product code NBW·September 14, 2010