BEUDAMED
    9 results · 35ms · Sources: EU EUDAMED, US FDA

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    KISH URETHRAL ILLUMINATED CATHETER SET

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    PIONEER SPINAL PROCESS FUSION PLATE

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    MODIFICATION TO TITANIUM TRI-LOCK HIPS STEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    L.C. 5000/CE NITROGL

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·July 27, 2009

    NITRO I.V. DC INF. SET W/LB TBG

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FRN·May 16, 2011

    L.C. 5000/CE NITROGLYCERIN PUM

    FDA Adverse Event
    Malfunction ·HOSPIRA COSTA RICA LTD.·Product code FPA·February 22, 2012

    CURLIN INFUSION IV PUMP

    FDA Adverse Event
    Malfunction ·MOOG MEDICAL DEVICES GROUP·Product code FRN·April 11, 2014

    OT ULTRALINK METER

    FDA Adverse Event
    Malfunction ·LIFESCAN INC.·Product code NBW·October 31, 2012

    MONOPLOAR CURVED SCISSORS INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·August 20, 2010