BEUDAMED
    6 results · 25ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.

    INSUFFLATION TUBING SET, PHX500-082

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PEAK FLOW MONITOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    HIGH SPEED MAGNETIC STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·December 22, 2010

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·February 4, 2014

    TOTALCARE BED

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·December 21, 2012