BEUDAMED
    6 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.
    Filters Regulation: Us FDA ×

    SWANSON TITANIUM CARPAL LUNATE IMPLANT

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    UVA SUNTANNING LAMPS

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    MEDIPART FILTER & TUBING MP-02X

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    IFUSE IMPLANT SYSTEM

    FDA Adverse Event
    Injury ·SI-BONE, INC.·Product code OUR·June 10, 2014

    UNKNOWN SPINAL CORD STIMULATOR

    FDA Adverse Event
    Injury ·MEDTRONIC NEUROMODULATION·Product code LGW·October 6, 2010

    EON MINI

    FDA Adverse Event
    Malfunction ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·December 6, 2012