BEUDAMED
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    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·December 22, 2018

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·October 20, 2018

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·November 24, 2017

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·September 28, 2018

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH HI-TEC·Product code LCP·August 31, 2017

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·November 16, 2018

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·December 27, 2017

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·January 17, 2019

    8031673-2017-00040

    FDA Adverse Event
    Malfunction ·September 30, 2017

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH HI-TEC·Product code KHO·October 11, 2017

    TOSOH AIA-360

    FDA Adverse Event
    Injury ·TOSOH HI-TEC·Product code KHO·July 1, 2016

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH HI-TEC·Product code LCP·August 14, 2017

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH HI-TEC·Product code KHO·September 6, 2017

    REVOGENE

    FDA Adverse Event
    Malfunction ·MERIDIAN BIOSCIENCE INC.·Product code OOI·November 5, 2025

    AIA-900

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·October 24, 2018

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·January 2, 2019

    AIA-900

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·December 20, 2018

    TOSOH HLC-723G8 ANALYZER

    FDA Adverse Event
    Malfunction ·TOSOH CORP.·Product code LCP·November 20, 2018

    TOSOH HLC-723G8 ANALYZER G8

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code LCP·December 7, 2018

    AIA-360

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·January 17, 2019