BEUDAMED
    8 results · 17ms · 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.

    ORGENTEC THYROGLOBULIN PIA (PIN IMMUNO ASSAY)

    FDA 510(k)
    FDA Class 2 ·Immunology

    APEX Revision Knee

    FDA UDI
    Omni Life Science, Inc.·00841690122722·Modular Stem 21mm x 75mm

    Sierra

    FDA UDI
    Seaspine Orthopedics Corporation·10889981095215·Occipital Tap, 8mm

    FLOWER HIGH-DENSITY MAPPING CATHETER, 4-4-4 MM ELECTRODE SPACING), (2-6-2 MM ELECTRODE SPACING)

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ORTHOPHOS SL

    FDA 510(k)
    FDA Class 2 ·Radiology

    CUTTING LOOP

    FDA Adverse Event
    Injury ·GYRUS ACMI, INC.·Product code HIH·February 6, 2013

    PRECISE PRO RX CAROTID STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIM·January 6, 2011

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·UNKNOWN·Product code CAW·July 22, 2014