BEUDAMED
    8 results · 25ms · Sources: EU EUDAMED, US FDA

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    VES-TEC/VES-MATIC

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    NAR

    FDA UDI
    NORTH AMERICAN RESCUE, LLC·00842209127665·

    Next Generation 088 Catheter

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    CARDIOVASCULAR SPRING GUIDE WIRE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    GORE® TAG® THORACIC ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code MIH·March 11, 2015

    MINICAP TRANSFER SET

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code KDJ·June 6, 2014

    SUPARTZ

    FDA Adverse Event
    Injury ·SEIKAGAKU CORPORATION·Product code MOZ·November 29, 2012

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·September 30, 2010