BEUDAMED
    9 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.

    125 I-DEHYDROEPIANDROSTERONE SULFATE

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    Tranquil-L™

    FDA UDI
    NEXUS SPINE, L.L.C.·B6788232000·DLIF Trial 12x22mm, 12 deg

    IdentiTi II

    FDA UDI
    ALPHATEC SPINE, INC.·00190376595634·ID II TLIF-A, STRAIGHT TAMP

    iNSitu™ Hip System

    FDA UDI
    NEXTSTEP ARTHROPEDIX, LLC·00816127020506·Head Trial 32mm x -4mm

    Curiteva Navigation System

    FDA 510(k)
    FDA Class 2 ·Neurology

    CERANUM 76

    FDA 510(k)
    FDA Class 2 ·Dental

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS·Product code JAA·March 20, 2014

    OT VERIO IQ METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·November 7, 2012

    CE INTERMATE LV 100, 24 PACK,50126

    FDA Adverse Event
    BAXTER HEALTHCARE - IRVINE·Product code FRN·September 1, 2010