BEUDAMED
    2,384 results · 26ms · Sources: EU EUDAMED, US FDA

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    UNKNOWN - OLYMPUS SINGLE BALLOON ENTEROSCOPE

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FDT·April 5, 2022

    UNKNOWN - OLYMPUS THERAPEUTIC DUODENOSCOPE

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FDT·April 5, 2022

    UNKNOWN - OLYMPUS SINGLE BALLOON ENTEROSCOPE

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FDT·April 5, 2022

    EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code ODG·April 5, 2022

    SPECTRA OPTIA

    FDA Adverse Event
    Injury ·TERUMO BCT·Product code LKN·April 25, 2023

    EVIS LUCERA SMALL INTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDA·February 18, 2026

    UNKNOWN - OLYMPUS THERAPEUTIC DUODENOSCOPE

    FDA Adverse Event
    Injury ·UNKNOWN·Product code FDT·April 5, 2022

    EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code ODG·April 5, 2022

    ACIST

    FDA Adverse Event
    Other ·ACIST MEDICAL SYSTEMS, INC.·Product code DXT·December 13, 2004

    V60 VENTILATOR

    FDA Adverse Event
    Malfunction ·RESPIRONICS CALIFORNIA, INC·Product code MNT·July 30, 2019

    PROTÉGÉ MRI IPG

    FDA Adverse Event
    Injury ·ST. JUDE MEDICAL - NEUROMODULATION (PUERTO RICO, LLC)·Product code LGW·November 1, 2023

    INDURA

    FDA Adverse Event
    Injury ·RICE CREEK MANUFACTURING·Product code LKK·January 3, 2007

    ENTERPRISE VASCULAR RECONSTRUCTION DEVICE AND DELIVERY SYSTEM

    FDA Adverse Event
    Injury ·CORDIS NEUROVASCULAR, INC.·Product code NJE·March 16, 2014

    SAVVY LONG OTW PTA CATHETER

    FDA Adverse Event
    Injury ·CLEARSTREAM TECHNOLOGIES LTD.·Product code LIT·May 28, 2019

    SAVVY LONG OTW PTA CATHETER

    FDA Adverse Event
    Malfunction ·CLEARSTREAM TECHNOLOGIES LTD.·Product code LIT·May 28, 2019

    SMART CONTROL NITINOL STENT SYSTEM 80 CM

    FDA Adverse Event
    Malfunction ·CORDIS DE MEXICO·Product code FGE·February 1, 2005

    PROCLAIM¿ 7 ELITE IMPLANTABLE PULSE GENERATOR

    FDA Adverse Event
    Injury ·ABBOTT MEDICAL·Product code LGW·January 4, 2024

    TI DISTRACTION LOCK

    FDA Adverse Event
    Injury ·SYNTHES BRANDYWINE·Product code MDI·March 2, 2012

    NORIAN DRILLABLE INJECT 5CC-STERILE

    FDA Adverse Event
    Malfunction ·SYNTHES MONUMENT·Product code MQV·February 22, 2015

    GRANUFLO

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·November 17, 2014