BEUDAMED
    98 results · 21ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·April 24, 2017

    EVIS X1 VIDEO SYSTEM CENTER

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FET·January 17, 2025

    EVIS EXERA II DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·October 6, 2021

    ENTERRA

    FDA Adverse Event
    Malfunction ·MEDTRONIC MED REL MEDTRONIC PUERTO RICO·Product code LNQ·July 1, 2013

    HEART LUNG MACHINE

    FDA Adverse Event
    Malfunction ·SORIN GROUP DEUTSCHLAND, (SORIN GROUP USA, INC. IS DISTRIBUTOR)·Product code DTQ·July 22, 2009

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    CAPSULE DEPLOYMENT DEVICE

    FDA Adverse Event
    Malfunction ·STERIS CORPORATION / UNITED STATES ENDOSCOPY GROUP·Product code NEZ·November 25, 2024

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    LARCRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORP.·Product code OKS·April 1, 2015

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORPORATION·Product code OKS·December 25, 2016

    EVIS EXERA II DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·November 22, 2020

    EVIS EXERA III GASTROINTESTINAL VIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDS·November 7, 2021

    OES CYSTONEPHROFIBERSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FAJ·March 10, 2021

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORP.·Product code OKS·February 13, 2015

    LACRIFAST

    FDA Adverse Event
    Malfunction ·KANEKA CORP.·Product code OKS·May 27, 2014

    EVIS EXERA III DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDT·February 16, 2023

    EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code ODG·October 21, 2021

    EVIS EXERA III DUODENOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FDT·December 23, 2021

    BARD TRI-FUNNEL REPLACEMENT GASTROSTOMY TUBE 24F

    FDA Adverse Event
    Malfunction ·BARD ACCESS SYSTEMS·Product code KNT·July 19, 2017