BEUDAMED
    9 results · 27ms · 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.

    KOAGULAB* 32-S COAGULATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Hematology

    Precept

    FDA UDI
    Nuvasive, Inc.·00887517426840·PRECEPT Screw, 5.0x35mm Fixed

    MAS PLIF

    FDA UDI
    Nuvasive, Inc.·00887517165220·MAS PLIF Screw, 5.0 x 35mm Polyaxial 3Z

    MEGA PLUS MIS SPINE SYSTEM

    FDA UDI
    BK MEDITECH CO.,LTD.·08809916495151·Long-arm Multi-Axial Cannulated Screw, Ø5.0 x 3...

    ELECTRODE FOR NEUROLOGICAL SURGERY 2111

    FDA 510(k)
    FDA Class 2 ·Neurology

    CALIBRATION REFERENCE I & II

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    G4 PLATINUM CONTINUOUS GLUCOSE MONITORING SYSTEM

    FDA Adverse Event
    Injury ·DEXCOM, INC.·Product code MDS·June 19, 2014

    MONARC SLING SYSTEM

    FDA Adverse Event
    Injury ·AMERICAN MEDICAL SYSTEMS, INC.·Product code FTL·December 18, 2012

    PULSE GEN MODEL 102

    FDA Adverse Event
    Malfunction ·CYBERONICS, INC.·Product code LYJ·October 20, 2010