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

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    Filters FDA Adverse Event ×

    SPECTRA WAVEWRITER

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·April 27, 2021

    NAIL HANDLE T2 TIBIA

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·March 3, 2016

    TROCAR, LONG T2 FEMUR

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·March 3, 2016

    WAVEWRITER ALPHA?

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION CORPORATION·Product code LGW·May 12, 2025

    OT SELECT SIMPLE METER

    FDA Adverse Event
    Injury ·LIFESCAN EUROPE, A DIVISION OF CILAG GMBH INTL·Product code NBW·April 23, 2013

    KAPPA 700 DR

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL, INC.·Product code DXY·July 10, 2008

    DA VINCI SI SURGICAL SYSTEM

    FDA Adverse Event
    Other ·INTUITIVE SURGICAL,INC.·Product code NAY·April 29, 2011

    1920898-2018-00830

    FDA Adverse Event
    Malfunction ·November 5, 2018

    BD SOLOMED¿ SYRINGE

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON IND. CIRURGICAS LTDA·Product code FMF·April 17, 2018

    9.0MM MEDULLARY REAMER HEAD

    FDA Adverse Event
    Injury ·SYNTHES SELZACH·Product code HTO·July 15, 2015

    5.0MM FLEXIBLE SHAFT

    FDA Adverse Event
    Injury ·SYNTHES BETTLACH·Product code HTO·July 15, 2015

    TIBIAL NAIL, STANDARD T2 TIBIA Ø9X360 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code HSB·March 3, 2016

    NAIL HOLDING SCREW, TIBIA T2 TIBIA 10 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·March 3, 2016