BEUDAMED
    8 results · 21ms · 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 ×

    Vitrea CT Cardiac Analysis

    FDA 510(k)
    FDA Class 2 ·Radiology

    LCP

    FDA UDI
    Synthes GmbH·10886982157409·4.5MM LCP® CONDYLAR PLATE 12 HOLES/278MM-RIGHT

    VERTIFLEX DIRECT DECOMPRESSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DIATEK CANNON-CATHETER, MODEL CC5500

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    LOGICAL 84" SINGLE MONITORING LINE

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL·Product code DRS·July 17, 2008

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·November 4, 2014

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·August 25, 2011

    PULSE GEN MODEL 103

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·July 12, 2013