BEUDAMED
    9 results · 20ms · Sources: EU EUDAMED, US FDA

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    COULTER AC.T DIFF ANALYZER

    FDA 510(k)
    FDA Class 2 ·Hematology

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·September 24, 2014

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 26, 2015

    COULTER ACT PAK REAGENT KIT

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER·Product code GKZ·May 5, 2015

    MULTIGENT CREATININE (ENZYMATIC) ASSAY

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    CELERITY 20 Steam Biological Indicator

    FDA 510(k)
    FDA Class 2 ·General Hospital

    CAMERA CORD

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL, INC.·Product code NAY·February 14, 2013

    SPRINT QUATTRO SECURE

    FDA Adverse Event
    Death ·MPRI·Product code LWS·August 1, 2014

    INTERSTIM II

    FDA Adverse Event
    Malfunction ·MDT PUERTO RICO OPERATIONS CO., JUNCOS·Product code EZW·January 18, 2011