BEUDAMED
    9 results · 22ms · Sources: EU EUDAMED, US FDA

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    GSI 70 AUDIOPATH SCREENER

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    KINAMED CTN STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    RAPID IMMOBILIZATION DEVICE OR R.I.D. SYSTEM

    FDA 510(k)
    FDA Class 1 ·General Hospital

    RADIESSE DERMAL FILLER

    FDA Adverse Event
    Other ·MERZ AESTHETICS, INC.·Product code LMH·February 13, 2013

    PRECISION TEST STRIPS

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE, INC. USA·Product code NBW·January 31, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code OYC·August 1, 2014

    CORTSCR Ø4.5 SELF-TAP L26 TI

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code HWC·June 6, 2013

    4.5MM CORTEX SCREW SELF-TAPPING 30MM

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 6, 2018

    CORTSCR Ø4.5 SELF-TAP L38 SST

    FDA Adverse Event
    Malfunction ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·April 6, 2018