BEUDAMED
    6 results · 17ms · 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.

    GX-MOBILE X-RAY UNIT

    FDA 510(k)
    FDA Class 2 ·Radiology

    FORTIFY Corpectomy Spacers

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODEL IV 100B-DA INFANT VENTILATOR

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 21, 2014

    CONTAK RENEWAL

    FDA Adverse Event
    Malfunction ·GUIDANT CRM CLONMEL IRELAND·Product code NIK·October 19, 2010

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·December 14, 2012