BEUDAMED
    9 results · 33ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ERBE

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code GEI·November 2, 2022

    MEDTRONIC INFUSE BONE GRAFT DEVICE (RHBMP-2)

    FDA Adverse Event
    MEDTRONIC, INC.·Product code NEK·March 28, 2013

    TERUMO ADVANCED PERFUSION SYSTEM 1

    FDA Adverse Event
    Malfunction ·TERUMO CARDIOVASCULAR SYSTEMS CORP.·Product code DTQ·March 7, 2011

    PKG STRL EVD SYSTEM (RAD)-NEW

    FDA Adverse Event
    Malfunction ·INTEGRA NEUROSCIENCES, PR·Product code JXG·April 16, 2008

    ERBE

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code GEI·March 8, 2023

    ERBE

    FDA Adverse Event
    Malfunction ·LEONHARD LANG GMBH·Product code GEI·February 18, 2025

    ACS HI-TORQUE BALANCE MIDDLEWEIGHT GUIDE WIRE WITH HYD

    FDA Adverse Event
    Malfunction ·ABBOTT VASCULAR-CARDIAC THERAPIES·Product code DQX·May 29, 2009

    ERBE

    FDA Adverse Event
    Injury ·LEONHARD LANG GMBH·Product code GEI·July 27, 2022

    BIOLOX® DELTA, CERAMIC FEMORAL HEAD, M, ø 36/0, TAPER 12/14

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code LZO·February 20, 2025