BEUDAMED
    11 results · 36ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    BONE SOURCE, HA CEMENT, 10 GM

    FDA Adverse Event
    Injury ·HOWMEDICA INC.·Product code GXP·July 18, 1997

    BONE SOURCE, HA CEMENT, 25 GM

    FDA Adverse Event
    Injury ·HOWMEDICA INC.·Product code LOD·July 18, 1997

    8010177-1996-00015

    FDA Adverse Event
    Malfunction ·Product code HXX·November 26, 1996

    DISTRACTION ROD FOR 18MM FRAME, L

    FDA Adverse Event
    Injury ·HOWMEDICA INC·Product code JEY·December 18, 1997

    L-PLATE, 100 DEGREE, 2MM BAR, RIGHT, GSP, 5 HOLE

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS FREIBURG·Product code HRS·October 23, 2007

    6.0MM ROD 500MM

    FDA Adverse Event
    Injury ·SYNTHES GMBH·Product code NKB·March 19, 2013

    M SERIES

    FDA Adverse Event
    Malfunction ·ZOLL MEDICAL CORPORATION·Product code MKJ·March 1, 2011

    PRECISION LINK

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC. USA·Product code NBW·March 10, 2008

    ENDOPATH ETS FLEX

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, INC.·Product code KOG·December 23, 1997

    ENDURANT

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·June 13, 2014

    ENDURANT ABDOMINAL STENT GRAFT SYSTEM

    FDA Adverse Event
    Death ·MEDTRONIC IRELAND·Product code MIH·February 8, 2013