BEUDAMED
    12 results · 54ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    NASAL ALAR SPO2 SENSOR

    FDA Adverse Event
    Malfunction ·XHALE ASSURANCE, INC·Product code DQA·November 6, 2017

    NASAL ALAR SPO2 SENSOR

    FDA Adverse Event
    Injury ·XHALE ASSURANCE, INC·Product code DQA·April 14, 2019

    NASAL ALAR SPO2 SENSOR

    FDA Adverse Event
    Injury ·XHALE ASSURANCE, INC·Product code DQA·April 14, 2019

    NASAL ALAR SP02 SENSOR

    FDA Adverse Event
    Malfunction ·XHALE ASSURANCE, INC.·Product code DQA·February 20, 2020

    NASAL ALAR SPO2 SENSOR

    FDA Adverse Event
    Injury ·XHALE ASSURANCE, INC·Product code DQA·July 8, 2019

    NASAL ALAR SPO2 SENSOR

    FDA Adverse Event
    Injury ·XHALE ASSURANCE, INC·Product code DQA·July 8, 2019

    NASAL ALAR SPO2 SENSOR

    FDA Adverse Event
    Injury ·XHALE ASSURANCE, INC·Product code DQA·July 9, 2019

    NASAL ALAR SPO2 SENSOR

    FDA Adverse Event
    Injury ·XHALE ASSURANCE, INC·Product code DQA·July 9, 2019

    NASAL ALAR SPO2 SENSOR

    FDA Adverse Event
    Injury ·XHALE ASSURANCE, INC·Product code DQA·July 9, 2019

    NASAL ALAR SPO2 SENSOR

    FDA Adverse Event
    Injury ·XHALE ASSURANCE, INC·Product code DQA·July 9, 2019

    NASAL ALAR SPO2 SENSOR

    FDA Adverse Event
    Injury ·XHALE ASSURANCE, INC·Product code DQA·July 9, 2019

    NASAL ALAR SPO2 SENSOR

    FDA Adverse Event
    Injury ·XHALE ASSURANCE, INC·Product code DQA·July 9, 2019