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 ×

    RESPIRATORY EXERCISOR, VOLUME PULSE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    IMPROVED COMFORT-FIT NIGHTGUARD

    FDA 510(k)
    FDA Unclassified ·Unknown

    ConvertX Biliary Stent System

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

    UNKNOWN DEPUY ASR ACETABULAR CUP

    FDA Adverse Event
    Injury ·DEPUY INTL., LTD - 8010379·Product code KWA·April 30, 2014

    MARYLAND BIPOLAR FORCEPS INSTRUMENT

    FDA Adverse Event
    Injury ·INTUITIVE SURGICAL,INC.·Product code NAY·October 10, 2012

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN, INC.·Product code MDS·August 3, 2010