BEUDAMED
    52 results · 23ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Injury ×

    ROSA SURGICAL DEVICE

    FDA Adverse Event
    Injury ·MEDTECH SA·Product code HAW·June 6, 2019

    NIM-ECLIPSE PREAMPLIFIER

    FDA Adverse Event
    Injury ·MEDTRONIC XOMED INC.·Product code GWF·January 11, 2018

    ROSA ONE BRAIN

    FDA Adverse Event
    Injury ·MEDTECH SAS·Product code HAW·January 23, 2025

    SYNCHROMED II

    FDA Adverse Event
    Injury ·MDT PUERTO RICO OPERATIONS CO·Product code LKK·October 5, 2016

    UNK - NAIL HEAD ELEMENTS: TFNA HELICAL BLADE

    FDA Adverse Event
    Injury ·DAI·Product code JDS·June 5, 2019

    SKYTRON

    FDA Adverse Event
    Injury ·DAI-ICHI·Product code FSY·May 15, 2015

    MAX GR 1X24 CV310 6/0 DA 1

    FDA Adverse Event
    Injury ·COVIDIEN, FORMERLY US SURGICAL A DIVISON·Product code GAM·June 3, 2016

    SKYTRON

    FDA Adverse Event
    Injury ·DAI-ICHI SHOMEI·Product code EBA·July 21, 2015

    SKYTRON

    FDA Adverse Event
    Injury ·DAI-ICHI SHOMI·Product code FSY·April 30, 2015

    SURGICAL LIGHT, CEILING MOUNTED

    FDA Adverse Event
    Injury ·DKK DAI-ICHI SHOMEI·Product code FSY·October 21, 2025

    LUMOS

    FDA Adverse Event
    Injury ·DKK DAI-ICHI SHOMEI·Product code FSY·February 7, 2025

    SKYTRON

    FDA Adverse Event
    Injury ·DAI-ICHI SHOMEI CO·Product code FSY·April 8, 2015

    MAX GR 1 X 30 CV301 5/0 DA 1% SS

    FDA Adverse Event
    Injury ·GOSPORT-USS·Product code GAN·August 22, 2005

    SKYTRON

    FDA Adverse Event
    Injury ·DAI-ICHI SHOMEI CO. LTD·Product code FSY·August 26, 2020

    SKYTRON

    FDA Adverse Event
    Injury ·DAI-ICHI SHOMEI CO., LTD·Product code FSY·July 31, 2018

    SKYTRON

    FDA Adverse Event
    Injury ·DAI-ICHI SHOMEI CO., LTD·Product code FSY·July 31, 2018

    LUMOS

    FDA Adverse Event
    Injury ·DKK DAI-ICHI SHOMEI CO., LTD.·Product code FSY·July 26, 2024

    LUMOS

    FDA Adverse Event
    Injury ·DKK DAI-ICHI SHOMEI CO., LTD.·Product code FSY·July 26, 2024

    STELLAR SERIES

    FDA Adverse Event
    Injury ·DKK DAI-ICHI SHOMEI CO., LTD.·Product code FSY·December 19, 2019

    BARDEX LUBRI-SIL I.C. ALL-SILICONE FOLEY CATHETER

    FDA Adverse Event
    Injury ·C.R. BARD, INC. (COVINGTON) -1018233·Product code EZL·July 1, 2020