BEUDAMED
    6 results · 21ms · 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.
    Filters Regulation: Us FDA ×

    CORSTREN COMPRESSION TUBE & PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DYONICS POWER CONTROL UNIT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    SPEEDLOCK KNOTLESS FIXATION DEVICE, 3MM DRILL, 3MM+ DRILL, PATHFINDER OBTURATOR & SHARP TIPPED OBTURATOR, LOW PROFILE DR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    BIOGLUE SURGICAL ADHESIVE

    FDA Adverse Event
    Injury ·CRYOLIFE, INC.·Product code MUQ·May 23, 2014

    HOMECHOICE PRO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - LARGO·Product code FKX·November 13, 2012

    SECURE II MED/SURG BED

    FDA Adverse Event
    Malfunction ·STRYKER CORP, MEDICAL DIV·Product code FNL·September 2, 2010