BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    Reprocessed DePuy Mitek Ablation Wand

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

    RECAP HIP INSTRUMENTATION

    FDA UDI
    Biomet Uk Ltd·05019279049912·

    M2a-Magnum™

    FDA UDI
    Biomet Orthopedics, LLC·00887868573194·

    EOS

    FDA 510(k)
    FDA Class 2 ·Radiology

    SODIUM CHLORIDE INJECTION, 0.9%, USP 5 ML, 10 ML AMPULE

    FDA 510(k)
    FDA Class 2 ·General Hospital

    GMK-SPHERE FEMORAL COMPONENT SPHERE CEMENTED SIZE 6+ R

    FDA Adverse Event
    Injury ·MEDACTA INTERNATIONAL SA·Product code JWH·December 20, 2019

    FREESTYLE FREEDOM

    FDA Adverse Event
    Malfunction ·Product code NBW·July 23, 2011

    PROGRAMMING SOFTWARE

    FDA Adverse Event
    Malfunction ·CYBERONICS INC·Product code LYJ·June 17, 2013

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FKX·October 15, 2014