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

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    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    HEMOCCULT® ICT TEST DEVICE

    FDA Adverse Event
    Injury ·BECKMAN COULTER·Product code KHE·June 3, 2013

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 14, 2012

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 14, 2012

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 14, 2012

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 14, 2012

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 22, 2012

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 22, 2012

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 22, 2012

    2050010-2017-00001

    FDA Adverse Event
    Malfunction ·October 13, 2017

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 22, 2012

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 22, 2012

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 22, 2012

    RHEUMATOID FACTOR REAGENT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code DHR·February 22, 2012