BEUDAMED
    5 results · 28ms · Sources: EU EUDAMED, US FDA

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    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS, INC.·Product code NBC·April 18, 2013

    QC F/K-WIRES Ø0.6-3.2 F/532.001 532.010

    FDA Adverse Event
    Malfunction ·SYNTHES OBERDORF·Product code HWE·July 10, 2017

    HORIZON ML ENDO APPLIER

    FDA Adverse Event
    Malfunction ·TELEFLEX·Product code FZP·January 31, 2013

    LANX SPINAL FIXATION SYSTEM

    FDA Adverse Event
    Injury ·LANX, INC·Product code NKB·January 24, 2011

    32MM M2A HI CARBON HEAD STANDARD NK

    FDA Adverse Event
    Injury ·BIOMET ORTHOPEDICS·Product code KWY·July 31, 2014