BEUDAMED
    6 results · 18ms · Sources: EU EUDAMED, US FDA

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    COVERSLIPPER

    FDA 510(k)
    FDA Class 1 ·Pathology

    IMPULSE IQ ADJUSTING INSTRUMENT

    FDA 510(k)
    FDA Unclassified ·Unknown

    DETECTOR, MODEL LC-100 FLUORESCENCE

    FDA 510(k)
    FDA Class 1 ·Clinical Chemistry

    OCTRODE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·October 5, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·July 12, 2007

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·December 3, 2013