BEUDAMED
    7 results · 35ms · Sources: EU EUDAMED, US FDA

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    LS-260G MONITOR/RECORDER & DEFIBILLATOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    omni TRAX Active Patient Tracker

    FDA 510(k)
    FDA Class 2 ·Radiology

    INTEGRITY, MODEL V500

    FDA 510(k)
    FDA Class 2 ·Neurology

    9600

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC0·Product code JAA·March 14, 2014

    EON

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 15, 2012

    KIMBERLY CLARK

    FDA Adverse Event
    Injury ·KIMBERLY CLARK·Product code KNT·September 22, 2010

    Pipeline Flex Embolization Device

    FDA Enforcement
    Class I ·Ongoing·Micro Therapeutics Inc,·September 15, 2021