BEUDAMED
    6 results · 22ms · 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 ×

    MICROSTREAM NASAL CANNULA FILTERLINE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Single Use MultiClip Device

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

    IGROK

    FDA 510(k)
    FDA Class 2 ·Radiology

    AMBIENT HIPVAC 50 WAND WITH INTEGRATED FINGER

    FDA Adverse Event
    Malfunction ·ARTHROCARE CORPORATION·Product code GEI·February 22, 2013

    V.A.C. THERAPY SYSTEM

    FDA Adverse Event
    Injury ·KCI USA, INC.·Product code OMP·February 3, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·August 5, 2014