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.

    IN-VITRO TEST FOR THE DETERMINATION OF CREATININE

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209127191·

    H.R. JAKOBI SURG. INSTR. #10 34/36

    FDA 510(k)
    FDA Class 1 ·Neurology

    SAYA 86 Radial Access Guide Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MIS SINGLE INNER SETS SCREW

    FDA Adverse Event
    Malfunction ·DEPUY SYNTHES SPINE·Product code NKB·June 6, 2014

    LAMITRODE S8

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 28, 2012

    LIGHTSPEED

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS, LLC·Product code JAK·September 3, 2010