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

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    CUI TISSUE EXPANDER VERSAFIL(TM) TISSUE EXPANDER

    FDA 510(k)
    FDA Unclassified ·Unknown

    IntelliBridge

    FDA UDI
    Philips Medical Systems Hsg·00884838090811·IntelliBridge EC40/80

    EMDS TOTAL CK TEST PACK-#67670/95

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    BERKOWITS 2200 SHORT WAVE (THERMOLYSIS EPILATOR)

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

    PORTEX PULSATOR PLUS ARTERIAL BLOOD SAMPLING

    FDA Adverse Event
    Malfunction ·SMITHS MEDICAL ASD, INC.·Product code JKA·February 25, 2011

    OT PING METER

    FDA Adverse Event
    Malfunction ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·June 11, 2014

    GREENLIGHT ADDSTAT

    FDA Adverse Event
    Malfunction ·AMS INNOVATION CENTER - SILICON VALLEY·Product code GEX·October 6, 2010

    ATTAIN

    FDA Adverse Event
    Malfunction ·MPRI·Product code OJX·December 10, 2012

    SPRYSTEP VECTOR KAFO, Custom made device dynamic ankle-foot orthosis (KAFO) non locking, REF #s: 17VKCUS and 17VKCUSX

    FDA Enforcement
    Class II ·Completed·Townsend Design·January 17, 2024