BEUDAMED
    91 results · 37ms · 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 FDA Adverse Event ×

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·November 15, 2018

    CONTINU-FLO

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FPA·December 30, 2016

    AIA-2000

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

    AIA-2000

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

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·November 15, 2018

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·April 26, 2018

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 9, 2018

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·April 9, 2018

    A1A-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·April 9, 2018

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·April 16, 2018

    BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·December 10, 2019

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 28, 2018

    BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBE THROMBIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·December 10, 2019

    BD VACUTAINER® RAPID SERUM TUBE (RST) BLOOD COLLECTION TUBES THROMBIN

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code JKA·December 10, 2019

    A1A-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 29, 2018

    AIA-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 2, 2018

    A1A-2000

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·April 9, 2018

    AIA-900

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·October 13, 2018

    AIA-900

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·December 18, 2018

    AIA-900

    FDA Adverse Event
    Malfunction ·TOSOH CORPORATION·Product code KHO·March 8, 2018