BEUDAMED
    48 results · 56ms · Sources: EU EUDAMED, US FDA

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    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·July 6, 2021

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM FOR ADULTS

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·November 7, 1996

    SONICBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code LFL·June 28, 2021

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·April 16, 2021

    THUNDERBEAT OPEN FINE JAW

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·September 8, 2021

    SONICBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code LFL·March 31, 2021

    NUCLEUS 22 CHANNEL COCHLEAR IMPLANT SYSTEM FOR ADULTS

    FDA Adverse Event
    Injury ·COCHLEAR LTD.·Product code MCM·February 7, 1997

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP TYPE S

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·December 21, 2021

    SONICBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code LFL·July 7, 2021

    SONICBEAT 5 MM, 35 CM, INLINE GRIP

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code LFL·March 18, 2021

    ORTHOVISC

    FDA Adverse Event
    Injury ·ANIKA THERAPEUTICS, INC.·Product code MOZ·July 25, 2008

    EVIS LUCERA ELITE GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code FDS·June 3, 2024

    MENTOR STYLE 1000 SMOTH AND MODERATE PLUS PROFILE SMOOTH ROUND STYLE

    FDA Adverse Event
    Injury ·MENTOR WORLDWIDE LLC·Product code FTR·November 12, 2019

    BIOPATCH, UNKNOWN SIZE/PRODUCT ID

    FDA Adverse Event
    Injury ·INTEGRA NEUROSCIENCES PR·Product code FRO·April 13, 2023

    EVIS EXERA III BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code EOQ·November 18, 2024

    EVIS EXERA III BRONCHOVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code EOQ·November 18, 2024

    PERCEVAL SUTURELESS AORTIC HEART VALVE

    FDA Adverse Event
    Injury ·LIVANOVA CANADA CORP.·Product code DYE·February 10, 2016

    ASPIRATION NEEDLE

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code GDM·November 18, 2024

    SINGLE USE ELECTROSURGICAL KNIFE KD-612

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code KNS·October 22, 2024

    EVIS EXERA III BRONCHOFIBERVIDEOSCOPE

    FDA Adverse Event
    Injury ·AIZU OLYMPUS CO., LTD.·Product code EOQ·November 18, 2024