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

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    BBL DIRECTIGEN MENINGITIS TEST KIT

    FDA 510(k)
    FDA Class 2 ·Microbiology

    ENDO WINDOW HIGH FREQUENCY ELECTROCAUTERY DEVICE, MODEL EW018

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    CARDIOSCOPE

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    PENTA

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL - NEUROMODULATION·Product code GZB·May 9, 2014

    PLASMABLADE TISSUE DISSECTION DEVICE

    FDA Adverse Event
    Malfunction ·MEDTORNIC ADVANCED ENERGY LLC·Product code GEI·October 25, 2012

    INTEGRATED APD SET W/CASSETTE3-PRONG

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - MOUNTAIN HOME·Product code FKX·August 31, 2010