BEUDAMED
    7,172 results · 111ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 11, 2010

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 11, 2010

    0.8% RESOLVE PANEL A

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

    0.8% RESOLVE PANEL A

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

    0.8% RESOLVE PANEL A

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

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 7, 2010

    SURGISCREEN

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·October 5, 2009

    0.8% RESOLVE PANEL B

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 11, 2010

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 11, 2010

    RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·January 14, 2010

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·January 11, 2010

    0.8% SELECTOGEN

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 7, 2010

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·October 5, 2009

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 11, 2010

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code KSZ·January 11, 2010

    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

    0.8% RESOLVE PANEL A

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

    0.8% RESOLVED PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·September 17, 2009

    0.8% RESOLVE PANEL A

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code KSZ·January 11, 2010