BEUDAMED
    5,583 results · 34ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    VISERA ELITE XENON LIGHT SOURCE

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code NWB·March 21, 2024

    EVIS EXERA II ULTRASOUND GASTROVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code ODG·September 3, 2024

    EMBOZENE MICROSPHERES

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code NAJ·August 5, 2022

    MCKESSON ANESTHESIA CARE

    FDA Adverse Event
    Malfunction ·MCKESSON TECHNOLOGIES, INC.·Product code BSZ·September 3, 2015

    MCKESSON ANESTHESIA CARE

    FDA Adverse Event
    Malfunction ·MCKESSON TECHNOLOGIES INC.·Product code BSZ·August 12, 2015

    EVIS EXERA III VIDEO SYSTEM CENTER

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FET·April 17, 2024

    REZUM

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code KNS·September 17, 2024

    UNKNOWN

    FDA Adverse Event
    Injury ·BOSTON SCIENTIFIC CORPORATION·Product code GEX·September 19, 2024

    MCKESSON ANESTHESIA CARE

    FDA Adverse Event
    Malfunction ·MCKESSON TECHNOLOGIES, INC.·Product code BSZ·January 31, 2014

    MCKESSON ANESTHESIA CARE

    FDA Adverse Event
    Malfunction ·MCKESSON TECHNOLOGIES INC.·Product code BSZ·January 10, 2014

    MCKESSON ANESTHESIA CARE

    FDA Adverse Event
    Malfunction ·MCKESSON TECHNOLOGIES INC.·Product code BSZ·January 10, 2014

    MCKESSON ANESTHESIA CARE

    FDA Adverse Event
    Malfunction ·MCKESSON TECHNOLOGIES INC.·Product code BSZ·January 10, 2014

    SOLTIVE PREMIUM SUPERPULSED LASER SYSTEM

    FDA Adverse Event
    Malfunction ·GYRUS ACMI, INC.·Product code GEX·August 1, 2024

    URETERO-RENO FIBERSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FGB·November 18, 2022

    EVIS EXERA III XENON LIGHT SOURCE

    FDA Adverse Event
    Malfunction ·OLYMPUS MEDICAL SYSTEMS CORP.·Product code NWB·March 24, 2022

    ACCELERATE PHENO SYSTEM, ACCELERATE PHENOTEST BC KIT

    FDA Adverse Event
    Malfunction ·ACCELERATE DIAGNOSTICS, INC.·Product code PRH·October 23, 2019

    EVIS LUCERA ELITE COLONOVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code FDF·November 12, 2024

    VIDEO SYSTEM CENTER

    FDA Adverse Event
    Malfunction ·SHIRAKAWA OLYMPUS CO., LTD.·Product code FDF·July 1, 2024

    ELECTRODE, PACEMAKER, PERMANENT

    FDA Adverse Event
    Injury ·MPRI·Product code DTB·February 9, 2013

    ELECTRODE, PACEMAKER, PERMANENT

    FDA Adverse Event
    Injury ·MEDTRONIC PUERTO RICO OPERATIONS CO.·Product code DTB·February 9, 2013