BEUDAMED
    6 results · 20ms · 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 ×

    FOUNTAIN INFUSION CATHETER AND OCCLUDING GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    LASERSAT CO2

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

    GUAZE SPONGES

    FDA 510(k)
    FDA Unclassified ·Unknown

    SURGICAL SIMPLEX CEMENT

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LOD·February 22, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·August 1, 2014