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 ×

    DISPOSABLE INTROSSEOUS INFUSION NEEDLES

    FDA 510(k)
    FDA Class 2 ·General Hospital

    ProLift Expandable System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INPATH E2 COLLECTOR

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·January 14, 2013

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·December 2, 2010

    CORE IMPACTION DRILL

    FDA Adverse Event
    Injury ·STRYKER INSTRUMENTS-KALAMAZOO·Product code DZJ·July 3, 2014