BEUDAMED
    6 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    HIGH PRESSURE TUBING

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    MAXPOWER RELIEF

    FDA 510(k)
    FDA Class 2 ·Neurology

    REPROCESSED DIAMOND BURS

    FDA 510(k)
    FDA Class 2 ·Neurology

    RENAL - DISPOSABLE

    FDA Adverse Event
    Injury ·Product code KDJ·December 30, 2010

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

    FDA Adverse Event
    Malfunction ·INVACARE FLORIDA OPERATIONS·Product code CAW·July 17, 2014

    BATTERY 14.8V, 6.3 AH LI-ION BATTERY

    FDA Adverse Event
    Malfunction ·PHILIPS MEDICAL SYSTEMS·Product code MKJ·December 22, 2012