BEUDAMED
    8 results · 26ms · Sources: EU EUDAMED, US FDA

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    CORDIS HIGH-TORQUE TEMP. PERVENOUS LEAD W/DEPTH MA

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    NAR Kit

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209107131·KIT, SQUAD

    Endo-Model SL Knee Prosthesis System

    FDA UDI
    WALDEMAR LINK GmbH & Co. KG·04026575372348·Femoral Segment, lateral, cemented

    POWDERED LATEX PATIENT EXAMINATION GLOVES

    FDA 510(k)
    FDA Class 1 ·General Hospital

    MIM-Thin Client (mobile)

    FDA 510(k)
    FDA Class 2 ·Radiology

    SYSTEM, PERITONEAL, AUTOMATIC DELIVERY

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE·Product code FKX·June 5, 2014

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    UNKNOWN·Product code IKX·November 29, 2012

    LIGHT HANDLE ASSEMBLY

    FDA Adverse Event
    Malfunction ·STRYKER COMMUNICATIONS·Product code BRY·September 21, 2010