BEUDAMED
    6 results · 19ms · 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.
    Filters Regulation: Us FDA ×

    FLUID DRAINAGE WICK

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SOMATOSENSORY EVOKED POTENTIAL STIMULATOR

    FDA 510(k)
    FDA Class 2 ·Neurology

    INTRO-REDUCER (NASOGASTRIC TUBE)

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

    COULTER ACT DIFF ANALYZER

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·June 19, 2014

    ACCU-CHEK ® AVIVA TEST STRIPS

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code LFR·October 28, 2010

    ACCOLADE PLUS TMZF HIP STEM #6

    FDA Adverse Event
    Injury ·STRYKER ORHTOPAEDICS CORK·Product code MEH·December 18, 2012