BEUDAMED
    8 results · 21ms · Sources: EU EUDAMED, US FDA

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    HYDROFERA FEMORAL WICK

    FDA 510(k)
    FDA Unclassified ·Unknown

    NOUVELLE (TM) MODEL #901, SIZES 0-12, LEFT & RIGHT

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

    CEPTI-SEAL DRESSING CHANGE KIT FOR CENT VEN CATH

    FDA 510(k)
    FDA Class 1 ·General Hospital

    ENDOPATH DILATING TIP TROCAR

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code GCJ·July 31, 1997

    ZONA PLUS

    FDA Adverse Event
    Injury ·ZONA HEALTH·Product code BXB·March 25, 2013

    OMNIPOD INSULIN PUMP

    FDA Adverse Event
    Malfunction ·INSULET CORPORATION·Product code LZG·January 25, 2013

    APEX ARC HIP STEM

    FDA Adverse Event
    Injury ·OMNLIFE SCIENCE, INC.·Product code LZO·January 20, 2011

    PARADIGM REAL-TIME INSULIN INFUSION PUMP

    FDA Adverse Event
    Malfunction ·MEDTRONIC MINIMED·Product code OYC·August 1, 2014