BEUDAMED
    6 results · 19ms · 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 ×

    PRISMA DISPOSABLE U-SHAPED CANNULA

    FDA 510(k)
    FDA Class 1 ·Ophthalmic

    SURGICAL CO2 LASER SYSTEM #20/OPTICAL FOR ARTHROSC

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

    GLUCOSE(HEXOKINASE) REAGENT SET

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    MINICAP PREP KITS

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - CALI·Product code KDI·June 16, 2014

    TELIGEN

    FDA Adverse Event
    Injury ·GUIDANT CRM CLONMEL IRELAND·Product code LWS·October 19, 2010

    RESOLUTE INTEGRITY RX

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code NIQ·December 17, 2012