BEUDAMED
    6 results · 26ms · 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 ×

    UREA-PDA DISK

    FDA 510(k)
    FDA Class 1 ·Microbiology

    RAMPART O AND RAMPART P

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    OMNI~NEB; OMNI~MAX

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·May 13, 2014

    LYNX SYSTEM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC - MARLBOROUGH·Product code FTL·November 13, 2012

    BARDPORT MRI LOW PROFILE IMPLANTED PORT WITH ATTACHABLE 6.6F

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS, INC.·Product code LJT·August 25, 2010