BEUDAMED
    118 results · 40ms · Sources: EU EUDAMED, US FDA

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    SGARLATO LABS

    FDA Adverse Event
    Malfunction ·SGARLATO LABS·Product code JDW·March 30, 2007

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MEDTRONIC, INC., NEUROLOGICAL DIVISION·Product code LKK·August 22, 2005

    SYNCHROMED II

    FDA Adverse Event
    Other ·NEUROLOGICAL DIVISION, MEDTRONIC, INC.·Product code LKK·September 29, 2005

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·April 3, 2006

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·September 22, 2005

    SYNVISC

    FDA Adverse Event
    Injury ·GENZYME CORPORATION·Product code MOZ·September 20, 2005

    AUTOPHERESIS C PLASMAPHERESIS INSTRUMENT, A200

    FDA Adverse Event
    Injury ·BAXTER HEALTHCARE CORP.·Product code GKT·September 2, 2005

    VUELOCK SCREW INSERTER

    FDA Adverse Event
    Malfunction ·EBI·Product code HXX·October 17, 2007

    6.2MM TI CLICK'X MONOAXIAL PEDICLE SCREW 50MM THRD LENGTH

    FDA Adverse Event
    Injury ·SYNTHES MONUMENT·Product code NKB·April 21, 2010

    OPUSDUO

    FDA Adverse Event
    Injury ·LUMENIS·Product code GEX·April 13, 2006

    IAB : 8 FR - 40 CC

    FDA Adverse Event
    Injury ·ARROW INTL., INC.·Product code DSP·August 31, 2005

    5.5MM TI CANCELLOUS LOCKING SCREW 26MM THRD LENGTH

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·September 29, 2005

    SALUTE FIXATION DEVICE

    FDA Adverse Event
    Malfunction ·DAVOL INC., SUB. C.R. BARD, INC.·Product code GDW·September 2, 2005

    ANGEL WING 23GX3 /4X12IN TUBING

    FDA Adverse Event
    Other ·TYCO HEALTHCARE/KENDALL·Product code GJE·September 14, 2005

    SYNCHROMED II

    FDA Adverse Event
    Injury ·NEUROLOGICAL DIVISION, MEDTRONIC, INC.·Product code LKK·August 30, 2005

    J-VAC RESERVOIR

    FDA Adverse Event
    Injury ·ETHICON, INC.·Product code GCY·January 12, 2006

    MICROSENSOR VENTRICULAR CATHETER KIT

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC.·Product code GWM·September 21, 2005

    HIRES 90K

    FDA Adverse Event
    Injury ·ADVANCED BIONICS CORP.·Product code MCM·September 12, 2005

    SELOX SR 45

    FDA Adverse Event
    Injury ·BIOTRONIK GMBH AND CO.,·Product code DTB·August 11, 2005

    NUCLEUS 24 CHANNEL COCHLEAR IMPLANT SYSTEM

    FDA Adverse Event
    Malfunction ·COCHLEAR LTD.·Product code MCM·October 10, 2005