BEUDAMED
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    Filters FDA Adverse Event ×

    VISIGLIDE GUIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 8, 2021

    PENCIL, H2K, PUSHBUTTON

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT·Product code GEI·September 10, 2020

    PENCIL, H2K, PUSHBUTTON

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT·Product code GEI·November 23, 2020

    DIPHENHYDRAMINE HCK, DIPHENHYDRAMINE

    FDA Adverse Event
    Product code ---·April 3, 2019

    PENCIL, H2K, PUSHBUTTON

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT COMPANY·Product code GEI·April 13, 2023

    SINGLE USE GUIDWIRE

    FDA Adverse Event
    Malfunction ·TERUMO CORPORATION, ASHITAKA·Product code OCY·March 17, 2021

    VISIGLIDE GUIDEWIRE

    FDA Adverse Event
    Injury ·TERUMO CORPORATION, ASHITAKA·Product code DQX·November 8, 2021

    SINGLE USE REPOSITIONABLE CLIP

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·March 9, 2023

    SINGLE USE REPOSITIONABLE CLIP

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·March 9, 2023

    SINGLE USE BILIARY STENT V

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code FGE·August 19, 2021

    SINGLE USE REPOSITIONABLE CLIP

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·March 9, 2023

    SINGLE USE REPOSITIONABLE CLIP

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·March 10, 2023

    SINGLE USE REPOSITIONABLE CLIP

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·March 10, 2023

    SINGLE USE REPOSITIONABLE CLIP

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code PKL·March 10, 2023

    COTILO PRESSFIT-HAK CEDIOR 48

    FDA Adverse Event
    Injury ·ZIMMER GMBH·Product code KWA·November 14, 2014

    SINGLE USE ROTATABLE CLIP FIXING DEVICE

    FDA Adverse Event
    Injury ·OLYMPUS MEDICAL SYSTEMS CORPORATION·Product code GDO·March 21, 2012

    SINGLE USE 3-LUMEN NEEDLE KNIFE V

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code KNS·June 29, 2022

    DRIVE

    FDA Adverse Event
    Injury ·LERADO H.K. LTD.·Product code INI·May 8, 2023

    DRIVE DEVILBISS HEALTHCARE

    FDA Adverse Event
    Injury ·LERADO H.K. LIMITED·Product code INI·February 22, 2024

    DRIVE

    FDA Adverse Event
    Injury ·LERADO H.K. LTD.·Product code INI·October 10, 2022