BEUDAMED
    42 results · 66ms · Sources: EU EUDAMED, US FDA

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    INDICAID health Sexual Health 2

    FDA UDI
    Phase Diagnostics, Inc.·00810113420028·A collection of noninvasive devices intended to...

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·December 28, 2009

    ANTI-D FOR SLIDE AND MODIFIED TUBE TESTS

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·December 28, 2009

    BREATHTEK UBT COLLECTION KIT

    FDA Adverse Event
    Other ·MERETEK DIAGNOSTICS, INC.·Product code MSQ·April 23, 2007

    ANTI-D BIOCLONE

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·August 10, 2009

    BREATHTEK UBT COLLECTION KIT

    FDA Adverse Event
    Other ·MERETEK DIAGNOSTICS, INC.·Product code MSQ·January 17, 2007

    SOUNDSTAR® ECO DIAGNOSTIC ULTRASOUND CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code OBJ·June 25, 2024

    SOUNDSTAR® ECO DIAGNOSTIC ULTRASOUND CATHETER

    FDA Adverse Event
    Injury ·BIOSENSE WEBSTER INC·Product code OBJ·June 17, 2024