BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    BARE-FIBER ENDOILLUMINATOR

    FDA 510(k)
    FDA Class 2 ·Ophthalmic

    SeaSpine Spacer System - Ventura™

    FDA UDI
    Seaspine Orthopedics Corporation·10889981033279·Ventura Trial, 9mm x 28mm x 15mm

    INTERLOCK-35 FIBERED IDC OCCLUSION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    IVY DEVICES INC. IV/MEDICAL LINE STABILIZER

    FDA 510(k)
    FDA Class 2 ·General Hospital

    TI N-FLEX ROD 150MM-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code NQP·December 14, 2010

    NEUROTHERM RF DISPOSABLE GROUNDING PAD

    FDA Adverse Event
    Other ·NEUROTHERM·Product code GXD·January 10, 2013

    PERCLOSE PROGLIDE 6F SUTURE MEDIATED CLOSURE (SMC) SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code MGB·July 14, 2014