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

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    Advanced Skin Renewing Device

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

    TROCHANTERIC NAIL KIT, TI GAMMA3 11X200MM X 125

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·November 7, 2012

    GRAFTYS HBS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MYOSURE XL TISSUE REMOVAL DEVICE (1 PACK) MYOSURE XL TISSUE REMOVAL DEVICE (3 PACK)

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    GRAFTYS HBS (510K NUMBER: K082498)

    FDA Adverse Event
    Injury ·GRAFTYS·Product code MQV·July 11, 2013

    PORTABLE OXYGEN GENERATOR (CONCENTRATOR, HOMEFILL)

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

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·June 14, 2013

    ACROBAT-I STABILIZER

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC.·Product code MWS·July 11, 2011