BEUDAMED
    195 results · 101ms · Sources: EU EUDAMED, US FDA

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    DIMENSION VISTA 1500

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE DIAGNOSTICS INC.·Product code JJE·October 24, 2018

    DEXTRUS 4136

    FDA Adverse Event
    Injury ·BIOTRONIK SE & CO. KG·Product code NVN·November 10, 2014

    EON MINI IPG, 16-CHANNEL RECHARGEABLE

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 7, 2011

    PENTA 3 MM LEAD, 60 CM

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 7, 2011

    ENDOWRIST

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·April 6, 2023

    TROCAR SLEEVE 12/110MM THREADED WITH TAP

    FDA Adverse Event
    Malfunction ·AESCULAP AG·Product code GCI·October 17, 2018

    ACTIVA

    FDA Adverse Event
    Malfunction ·NEURO - VILLALBA·Product code MHY·February 18, 2013

    INFINION CX

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC NEUROMODULATION·Product code LGW·September 7, 2020

    BONE PLATE, MP, 4 HOLE, MEDIUM BAR

    FDA Adverse Event
    Malfunction ·STRYKER LEIBINGER FREIBURG·Product code JEY·December 5, 2013

    EON IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Malfunction ·ADVANCED NEUROMODULATION SYSTEMS·Product code LGW·June 1, 2010

    ILLUMINA MISEQDX INSTRUMENT

    FDA Adverse Event
    Injury ·ILLUMINA HAYWARD·Product code PFF·September 10, 2025

    LAMITRODE 44 SURGICAL LEAD

    FDA Adverse Event
    Malfunction ·ST JUDE MEDICAL - NEUROMODULATION·Product code LGW·November 23, 2010

    REFLEX HYBRID SCREW EXTRACTOR INNER SHAFT

    FDA Adverse Event
    Malfunction ·STRYKER SPINE BORDEAUX·Product code HWC·November 17, 2011

    NA

    FDA Adverse Event
    Malfunction ·STRYKER SUSTAINABILITY SOLUTIONS LAKELAND·Product code NLM·August 11, 2014

    LAMITRODE 8 PADDLE LEAD

    FDA Adverse Event
    Injury ·ADVANCED NEUROMODULATION SYSTEMS, INC.·Product code LGW·August 31, 2010

    LIGATURE CUTTER L:125MM

    FDA Adverse Event
    Injury ·AESCULAP AG·Product code DZC·September 20, 2022

    *

    FDA Adverse Event
    Other ·S.U.A. MARTIN GMBH&CO.KG·Product code HTX·August 12, 2008

    VIGILA 1CR 65 CE

    FDA Adverse Event
    Malfunction ·BIOTRONIK SE & CO. KG·Product code NVY·November 24, 2015

    SHARK

    FDA Adverse Event
    Malfunction ·RICHARD WOLF GMBH·Product code FAS·May 6, 2021

    NA

    FDA Adverse Event
    Injury ·STRYKER-ENDOSCOPY LAKELAND 5300·Product code NLM·April 22, 2024