BEUDAMED
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    ITM

    FDA Adverse Event
    Death ·SULZER INTERMEDICS INC.·Product code DTB·August 19, 1998

    ARTIS ZEEGO

    FDA Adverse Event
    Malfunction ·SIEMENS HEALTHCARE GMBH·Product code OWB·October 20, 2017

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

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·November 8, 2023

    SOUNDBITE HEARING SYSTEM

    FDA Adverse Event
    Injury ·SONITUS MEDICAL·Product code LXB·August 9, 2013

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

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·September 6, 2022

    PUMP INSTYLE (ITME #UNK)

    FDA Adverse Event
    Malfunction ·MEDELA, INC.·Product code HGX·May 13, 2015

    DAVINCI XI

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC·Product code NAY·March 31, 2025

    PYXIS MEDSTATION ES SYSTEM

    FDA Adverse Event
    Malfunction ·CAREFUSION 303·Product code BRY·January 9, 2025

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

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·June 10, 2022

    SONICBEAT 5 MM, 45 CM, FRONT-ACTUATED GRIP

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code LFL·August 29, 2023

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

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code GEI·June 13, 2023

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

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·March 2, 2023

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

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·March 2, 2023

    THUNDERBEAT OPEN EXTENDED JAW

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·March 2, 2023

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

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·May 3, 2023

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

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code GEI·December 9, 2022

    THUNDERBEAT OPEN EXTENDED JAW

    FDA Adverse Event
    Injury ·AOMORI OLYMPUS CO., LTD.·Product code GEI·October 11, 2023

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

    FDA Adverse Event
    Malfunction ·AOMORI OLYMPUS CO., LTD.·Product code GEI·September 23, 2022

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

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code GEI·March 1, 2022

    INTERLINK CATHETER EXTENSION SET

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP.·Product code FOZ·January 7, 2005