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

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    MODEL E278OR-ASP SERIES RETRACTABLE

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    SENSIDERM

    FDA 510(k)
    FDA Class 1 ·General, Plastic Surgery

    DERATA MEDI-JECTOR PRO

    FDA 510(k)
    FDA Class 2 ·General Hospital

    7700

    FDA Adverse Event
    Malfunction ·GE MEDICAL SYSTEMS (INDIA) PRIVATE LTD·Product code JAA·December 6, 2010

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·January 9, 2013

    ANIMAS VIBE

    FDA Adverse Event
    Malfunction ·ANIMAS CORPORATION·Product code LZG·July 18, 2014

    ev3 Pipeline Flex Embolization Device. For neurological endovascular use.

    FDA Enforcement
    Class I ·Terminated·Micro Therapeutics Inc, Dba Ev3 Neurovascular·April 1, 2020