BEUDAMED
    9 results · 21ms · Sources: EU EUDAMED, US FDA

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    RENASYS GO

    FDA Adverse Event
    Malfunction ·SMITH & NEPHEW, INC.·Product code OMP·December 29, 2010

    FEMORAL ACCESS DEVICE

    FDA Adverse Event
    Death ·EDWARDS LIFESCIENCES·Product code DWF·February 14, 2013

    CHARGING SYSTEM

    FDA Adverse Event
    Injury ·ST JUDE MED - NEUROMODULATION·Product code GZB·July 14, 2014

    CONTOUR ACETABULAR RECONSTRUCTION RING

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDJ·June 6, 2025

    MESH, SURGICAL, ACETABULAR, HIP, PROSTHESIS

    FDA Adverse Event
    Injury ·SMITH & NEPHEW, INC.·Product code JDJ·January 23, 2026

    SCREW, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES (USA)·Product code HWC·February 6, 2017

    BA102

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·March 31, 2016

    BA105

    FDA Adverse Event
    Malfunction ·NAKANISHI INC.·Product code EGS·March 28, 2016

    NSK

    FDA Adverse Event
    Injury ·NAKANISHI INC.·Product code EGS·August 29, 2017