BEUDAMED
    12 results · 31ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    9616240-2006-00344

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00342

    FDA Adverse Event
    Malfunction ·Product code KDI·June 14, 2006

    9616240-2006-00330

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    9616240-2006-00349

    FDA Adverse Event
    Malfunction ·Product code FII·June 21, 2006

    9616240-2006-00348

    FDA Adverse Event
    Malfunction ·Product code FDI·June 20, 2006

    *

    FDA Adverse Event
    Malfunction ·Product code FII·June 1, 2006

    9616240-2006-00346

    FDA Adverse Event
    Malfunction ·Product code FII·June 14, 2006

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019

    VERTEX RECONSTRUCTION SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWP·June 13, 2019

    STERLING¿

    FDA Adverse Event
    Malfunction ·BOSTON SCIENTIFIC - MAPLE GROVE·Product code DQY·March 19, 2013

    HAKIM PROG VALVE INLINE SIPHONGUARD

    FDA Adverse Event
    Injury ·CODMAN & SHURTLEFF, INC., MEDOS S.A.·Product code JXG·March 3, 2011

    RIATA ST ACTIVE FIXATION

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·March 10, 2008