BEUDAMED
    7 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 ×

    INTERMITTENT MANDATORY VENTILATION

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    Ophthalmic Cannula

    FDA UDI
    KATENA PRODUCTS, INC.·00841668110683·LUER ADAPTOR FOR IRRIGATION

    VisioFocus Mini, VisioFocus Smart

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ATRILAZE SURGICAL ABLATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    ERBE APC 2

    FDA Adverse Event
    Death ·ERBE ELEKTROMEDIZIN GMBH·Product code GEI·April 11, 2014

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER MEDICAL·Product code FNL·September 19, 2012

    MIDMARK

    FDA Adverse Event
    Malfunction ·MIDMARK CORP.·Product code EAZ·July 14, 2010