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

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    MSI 4000 SERIES BED

    FDA 510(k)
    FDA Class 2 ·General Hospital

    COLLIEVA

    FDA 510(k)
    FDA Unclassified ·Unknown

    Medline Reinforced Epidural Catheter

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    CLINITRON RITEHITE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·May 27, 2014

    AUTOMATED PD SET W/CASSETTE4 PRONG

    FDA Adverse Event
    Death ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·October 25, 2010

    AUTOPULSE RESUSCITATION SYSTEM MODEL 100

    FDA Adverse Event
    Malfunction ·ZOLL CIRCULATION, INC·Product code DRM·November 7, 2012