BEUDAMED
    7 results · 25ms · 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.

    DYNAMIC CARDIAC PHANTOM 74-347

    FDA 510(k)
    FDA Class 1 ·Radiology

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209122486·

    cobas liat CT/NG nucleic acid test

    FDA 510(k)
    FDA Class 2 ·Microbiology

    Microlyte Ag

    FDA 510(k)
    FDA Unclassified ·Unknown

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Malfunction ·DEXCOM, INC.·Product code MDS·June 6, 2014

    TOTAL ASR ACET IMP SIZE 50

    FDA Adverse Event
    Injury ·DEPUY INTERNATIONAL LTD - 8010379·Product code KWA·December 3, 2012

    POWERHEART AED G3

    FDA Adverse Event
    Malfunction ·CARDIAC SCIENCE CORPORATION·Product code MKJ·September 3, 2010