BEUDAMED
    6 results · 18ms · 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.

    RETRACTORS

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    TUBING, E.V.A. FLEXIBLE

    FDA 510(k)
    FDA Class 1 ·Anesthesiology

    APLIO ARTIDA V2.0 SSH-880CV

    FDA 510(k)
    FDA Class 2 ·Radiology

    LIBERTÉ?

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code MAF·June 24, 2014

    LEAD MODEL 302-20

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·October 22, 2010

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·December 28, 2012