BEUDAMED
    2,177 results · 25ms · Sources: EU EUDAMED, US FDA

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    OLYMPUS HYF-P FLEXIBLE HYSTEROFIBERSCOPE

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    Visera Hysterovideoscope Olympus HYF Type V

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    VISERA HYSTEROVIDEOSCOPE OLYMPUS HYF TYPE V

    FDA 510(k)
    FDA Class 2 ·Obstetrics/Gynecology

    VISERA HYSTEROVIDEOSCOPE

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170411564·VISERA HYSTEROVIDEOSCOPE

    OES HYSTEROFIBERSCOPE

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170307089·

    VISERA HYSTEROVIDEOSCOPE

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170458439·

    OES HYSTEROFIBERSCOPE

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170340178·HYF-XP HYSTEROFIBER SCOPE 3.1mm Diameter

    OES HYSTEROFIBERSCOPE

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170411090·OES HYSTEROFIBERSCOPE

    VISERA HYSTEROVIDEOSCOPE

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170340185·HYF-V Flexible Video Hysteroscope

    OES HYSTEROFIBERSCOPE

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170058219·

    OES HYSTEROFIBERSCOPE

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170411571·OES HYSTEROFIBERSCOPE

    OES HYSTEROFIBERSCOPE

    FDA UDI
    OLYMPUS MEDICAL SYSTEMS CORP.·04953170051128·HYF-1T HYS-Fiberscope 4.9mm dia w/chan

    VIDEO FLEXIBLE HYSTEROSCOPE

    FDA Adverse Event
    Malfunction ·OLYMPUS·Product code HIH·June 11, 2015

    FIBERSCOPE "HYF-XP"

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code HIH·February 3, 2024

    FIBERSCOPE "HYF-XP"

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code HIH·October 13, 2022

    VISERA HYSTEROVIDEOSCOPE

    FDA Adverse Event
    Malfunction ·AIZU OLYMPUS CO., LTD.·Product code HIH·July 5, 2023

    HYF HND SWTCH PENCL AUTOCLAVAB

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT·Product code GEI·April 16, 2019

    HYF HND SWTCH PENCL AUTOCLAVAB

    FDA Adverse Event
    Malfunction ·CONSOLIDATED MEDICAL EQUIPMENT·Product code GEI·July 26, 2018

    HYF HND SWTCH PENCL AUTOCLAVAB

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code GEI·January 9, 2018

    HYF HND SWTCH PENCL AUTOCLAVAB

    FDA Adverse Event
    Malfunction ·CONMED CORPORATION·Product code GEI·March 28, 2018