BEUDAMED
    10 results · 18ms · Sources: EU EUDAMED, US FDA

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    LM BONE ANCHOR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    PACING/PSI KIT: 5 FR/6 FR 2-L

    FDA Adverse Event
    Malfunction ·ARROW INTERNATIONAL INC.·Product code LDF·April 15, 2015

    LUNG FLUTE

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SunTech CT40 Spot-check Vital Signs Device

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CDS/R/4K DILUENT/SHEATH, 20L

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIV/CELLDYN·Product code GKL·April 12, 2007

    CD SAPPHIRE, CD 4000 SYSTEMS DILUENT/SHEATH

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIV/CELLDYN·Product code GKL·December 8, 2006

    CELL-DYN DILUENT/SHEATH

    FDA Adverse Event
    Malfunction ·ABBOTT DIAGNOSTICS DIVISION/CELLDYN·Product code GKL·January 5, 2007

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 9, 2014

    APEX MODULAR HIP SYSTEM

    FDA Adverse Event
    Injury ·OMNLIFE SCIENCE·Product code LPH·February 7, 2013

    PROFEMUR(R) MODULAR FEMORAL NECK

    FDA Adverse Event
    Injury ·WRIGHT MEDICAL TECHNOLOGY, INC.·Product code LPH·January 13, 2011