BEUDAMED
    7 results · 29ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·WRIGHTS LANE SYNTHES USA PRODUCTS LLC·Product code HWC·June 7, 2018

    NAIL, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES SELZACH·Product code JDS·February 13, 2017

    QUIK-COMBO PACING/DEFIBRILLATION/ECG

    FDA Adverse Event
    Malfunction ·PHYSIO-CONTROL CORP·Product code LDD·March 31, 1998

    RETRACTOR HANDLE

    FDA Adverse Event
    Malfunction ·SYNTHES (USA)·Product code GAD·April 11, 2013

    ACUITY

    FDA Adverse Event
    Malfunction ·CPI - DEL CARIBE·Product code OJX·April 12, 2011

    RINGLOC BI-POLAR CUP

    FDA Adverse Event
    Malfunction ·BIOMET, INC.·Product code JDI·May 20, 2008

    NAIL, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code JDS·July 5, 2016