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

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    NATURAL POROUS HIP SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    NA

    FDA UDI
    Stryker Leibinger GmbH & Co. KG·04546540355362·UNIVERSAL MAND. RECON MODULE

    Gen. Acces/ Instr. Tip Guard

    FDA UDI
    KATENA PRODUCTS, INC.·00841668112311·SURG-I-BAND BLUE

    UNITY TOATAL KNEE SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    ICS MEDICAL MODEL VG-30 VIDEO GOGGLES

    FDA 510(k)
    FDA Class 2 ·Neurology

    TRILOGY 100

    FDA Adverse Event
    Malfunction ·RESPIRONICS INC·Product code CBK·May 14, 2014

    SMART CONTROL NITINOL STENT SYSTEM

    FDA Adverse Event
    Injury ·CORDIS DE MEXICO·Product code NIO·December 2, 2010

    DOME TITANIUM SINGLE LUMEN PORT

    FDA Adverse Event
    Injury ·C.R. BARD INC.·Product code LJT·November 30, 2012

    MTS ANTI-A, B (MURINE MONOCLONAL BLEND) CARD

    FDA Adverse Event
    Malfunction ·MICROTYPING SYSTEMS·Product code KSZ·June 27, 2017