BEUDAMED
    7 results · 17ms · Sources: EU EUDAMED, US FDA

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    OMNICOR PROGRAMMER MODEL 222C

    FDA 510(k)
    FDA Class 3 ·Cardiovascular

    Revolution Peripheral Atherectomy System, Revolution Peripheral Atherectomy Guidewire

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    VICKS POWERSHOT DRY THROAT & MOUTH RELIEF

    FDA 510(k)
    FDA Unclassified ·Unknown

    ANIMAS INSULIN CARTRIDGE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·May 5, 2014

    VIRTUOSO DR

    FDA Adverse Event
    Injury ·MEDTRONIC S.A.·Product code LWS·October 15, 2012

    OEC 9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·August 6, 2010

    PROPONENT DR SL (Model L201)

    FDA Enforcement
    Class I ·Ongoing·Boston Scientific Corporation·October 22, 2025