BEUDAMED
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    Filters FDA Adverse Event ×

    SINGLE USE ASPIRATION NEEDLE

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code FCG·May 31, 2024

    SONICBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code LFL·June 28, 2021

    DISPOSABLE BALLOON CATHETER

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code EOQ·June 15, 2021

    SINGLE USE 3-LUMEN SPHINCTEROTOME V

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code KNS·June 24, 2021

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

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·June 22, 2022

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

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·June 22, 2022

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

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·June 22, 2022

    SINGLE USE ASPIRATION NEEDLE

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code FCG·December 2, 2021

    SINGLE USE MECHANICAL LITHOTRIPTOR V

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code LQC·May 20, 2022

    THUNDERBEAT 5 MM, 20 CM, FRONT-ACTUATED GRIP TYPE S

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·June 22, 2022

    SONICBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code LFL·May 10, 2021

    SINGLE USE MECHANICAL LITHOTRIPTOR V

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code LQC·July 8, 2024

    THUNDERBEAT OPEN FINE JAW TYPE X

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·September 6, 2024

    BILIARY DRAINAGE TUBE

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code FGE·September 6, 2024

    SONICBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code LFL·July 23, 2024

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·August 2, 2024

    DISPOSABLE DISTAL ATTACHMENT

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code FDS·September 13, 2024

    SINGLE USE ASPIRATION NEEDLE

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code FCG·August 5, 2024

    THUNDERBEAT 5 MM, 35 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code GEI·August 22, 2024

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

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code GEI·August 29, 2024