BEUDAMED
    10 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    ALL-POLY TRI POLAR CUP 26X60MM

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·December 28, 2017

    INTERVERTEBRAL FUSION DEVICE WITH BONE GRAFT, LUMBAR

    FDA Adverse Event
    Injury ·MEDTRONIC SOFAMOR DANEK, INC.·Product code MAX·May 9, 2019

    ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Injury ·WARSAW ORTHOPEDICS·Product code KWQ·May 10, 2018

    RLOC TRIPOLAR 41MMOD28MMIDSZ26

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·March 14, 2018

    RINGLOC TRI-POLAR ACETABULAR SHELL

    FDA Adverse Event
    Injury ·ZIMMER BIOMET, INC.·Product code KWY·May 23, 2018

    ATRICURE BIPOLAR SYSTEM

    FDA Adverse Event
    Injury ·ATRICURE, INC.·Product code GEI·July 28, 2010

    ZIMMER SKIN GRAFT MESHER COMPLETE

    FDA Adverse Event
    Malfunction ·ZIMMER SURGICAL·Product code FZW·April 11, 2013

    TOTALCARE

    FDA Adverse Event
    Malfunction ·HILL-ROM, INC.·Product code FNL·March 16, 2011

    NOVASURE IMPEDANCE CONTROLLED EA SYSTEM

    FDA Adverse Event
    Injury ·CYTYC SURGICAL PRODUCTS·Product code MNB·June 20, 2008

    VENTURE ANTERIOR CERVICAL PLATE SYSTEM

    FDA Adverse Event
    Malfunction ·MDT SOFAMOR DANEK PUERTO RICO MFG·Product code KWQ·February 10, 2025