BEUDAMED
    11 results · 26ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    CHAMBER COMPLETE AUTOFEED 900

    FDA Adverse Event
    Malfunction ·Product code BTT·May 5, 2021

    CHAMBER COMPLETE AUTOFEED 900

    FDA Adverse Event
    Malfunction ·Product code BTT·January 21, 2020

    NATURALYTE

    FDA Adverse Event
    Death ·FRESENIUS MEDICAL CARE NORTH AMERICA·Product code KPO·June 27, 2014

    ISERT ASPHERIC INTRAOCULAR LENS

    FDA Adverse Event
    Malfunction ·HOYA SURGICAL OPTICS, INC.·Product code HQL·December 8, 2010

    9800

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·January 3, 2013

    VENTED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·July 17, 2023

    VENTED AUTOFEED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·February 20, 2023

    VENTED AUTOFEED HUMIDIFICATION CHAMBER

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·January 23, 2024

    CHAMBER COMPLETE AUTOFEED 900

    FDA Adverse Event
    Malfunction ·Product code BTT·June 3, 2021

    FISHER & PAYKEL HEALTHCARE

    FDA Adverse Event
    Malfunction ·FISHER & PAYKEL HEALTHCARE LTD·Product code BTT·May 15, 2024

    CHAMBER COMPLETE AUTOFEED 900

    FDA Adverse Event
    Malfunction ·Product code BTT·February 4, 2021