BEUDAMED
    7,799 results · 29ms · Sources: EU EUDAMED, US FDA

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    GUIDE WIRE, 300MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS SELZACH·Product code HTY·January 4, 2010

    NA

    FDA Adverse Event
    Malfunction ·STRYKER TRAUMA SA·Product code LXH·June 28, 2021

    *

    FDA Adverse Event
    Malfunction ·DEPUY-ACE MEDICAL·Product code HXI·January 6, 1998

    VITEK® 2 GRAM NEGATIVE IDENTIFICATION TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code LQM·October 11, 2018

    EXACTAMIX 2400 COMPOUNDER

    FDA Adverse Event
    Other ·BAXA CORP.·Product code LHI·April 25, 2011

    GRAM NEGATIVE PANEL

    FDA Adverse Event
    Death ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code LRG·June 20, 2013

    VITEK® 2 GN TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMERIEUX INC.·Product code JTO·December 13, 2016

    K-WIRE, RECON ?3.2X400 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·November 21, 2008

    BAXTER

    FDA Adverse Event
    Injury ·*·Product code FRN·April 5, 2004

    SPINEMAP® 3D 3.1 - SOFTWARE

    FDA Adverse Event
    Malfunction ·STRYKER INSTRUMENTS-A DIVISION OF STRYKER CORP·Product code HAW·February 18, 2022

    ABL800 FLEX

    FDA Adverse Event
    Malfunction ·RADIOMETER MEDICAL APS·Product code CHL·November 9, 2021

    UNK

    FDA Adverse Event
    Malfunction ·UNK·Product code HTY·November 1, 2001

    UNK

    FDA Adverse Event
    Injury ·UNK·Product code HTY·October 4, 2007

    PLATE, FIXATION, BONE

    FDA Adverse Event
    Injury ·SYNTHES USA·Product code HRS·February 2, 2017

    *

    FDA Adverse Event
    ACUMED·Product code HTY·February 3, 2012

    WIRE FX KIRSCHNER

    FDA Adverse Event
    Product code HTY·August 31, 2020

    UNK

    FDA Adverse Event
    Malfunction ·UNK·Product code HTY·November 1, 2001

    K-WIRE 3-4MM

    FDA Adverse Event
    Injury ·Product code LXH·February 27, 2014

    K-WIRE

    FDA Adverse Event
    Malfunction ·ZIMMER, INC.·Product code HTY·August 18, 1998

    K-WIRE, RECON 3.2X400 MM

    FDA Adverse Event
    Malfunction ·STRYKER OSTEOSYNTHESIS KIEL·Product code LXH·July 21, 2011