BEUDAMED
    8 results · 22ms · Sources: EU EUDAMED, US FDA

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    CAPSTONE L SPINAL SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NITRILE EXAMINATION GLOVES, POWDER FREE

    FDA 510(k)
    FDA Class 1 ·General Hospital

    OSTEOBRIDGE IKA KNEE ARTHODESIS NAIL WITH COLLAR

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    U-BLADE SET, TI GAMMA3 10.5X90MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·November 30, 2012

    IMPLANTED TRIFUSION CATHETER

    FDA Adverse Event
    Malfunction ·C. R. BARD INC. (BASD)·Product code LJS·May 15, 2013

    K-WIRE, COCR, RECON T2 RECON Ø3.2X400 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·September 27, 2014

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Death ·MEDTRONIC PUERTO RICO, INC.·Product code LWS·June 14, 2011

    STEALTHSTATION TRIA

    FDA Adverse Event
    Injury ·MEDTRONIC NAVIGATION, INC. (LOUISVILLE)·Product code HAW·May 31, 2017