BEUDAMED
    7 results · 27ms · 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.

    BLADE, SCALPEL

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209131372·

    WI-38 GENCELLS

    FDA 510(k)
    FDA Class 1 ·Hematology

    BARD URETEROSCOPIC CYTOLOGY BRUSH

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

    CARPENTIER-EDWARDS PERIMOUNT PLUS PERICARDIAL BIOPROSTHESIS

    FDA Adverse Event
    Injury ·EDWARDS LIFESCIENCES·Product code DYE·June 6, 2014

    VISIONAIRE

    FDA Adverse Event
    Malfunction ·AIRSEP CORP.·Product code CAW·November 29, 2012

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS INNOVATION CENTER-SILICON VALLEY·Product code GEX·September 30, 2010