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

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    K-WIRE STRYKER 3.2MM X 450MM KIRSCHNER

    FDA Adverse Event
    Malfunction ·Product code LXH·November 2, 2021

    K-WIRE GAMMA Ø3,2X450 MM

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA KIEL·Product code LXH·April 22, 2022

    CONTOUR CURVED CUTTER STAPLER CS

    FDA Adverse Event
    Malfunction ·ETHICON ENDO SURGERY, INC.(CINCINNATI)·Product code GDW·June 13, 2006

    BD NEXIVA 24 GA X 3/4 IN SINGLE PORT

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON INFUSION THERAPY SYSTEMS INC.·Product code FOZ·May 30, 2024

    ACCU-CHEK SPIRIT COMBO

    FDA Adverse Event
    Malfunction ·ROCHE DIABETES CARE AG·Product code LZG·April 8, 2013

    SELECT SECURE

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO, INC.·Product code NVN·April 5, 2011

    SHILEY FEN L-P-C

    FDA Adverse Event
    Injury ·COVIDIEN/FORMERLY TYCO·Product code BTO·May 7, 2008