BEUDAMED
    177 results · 81ms · Sources: EU EUDAMED, US FDA

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    VITROS CHEMISTRY PRODUCTS CKMB SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code JHS·May 18, 2023

    VITROS CHEMISTRY PRODUCTS CKMB SLIDES

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code JHS·May 18, 2023

    VITROS DT60 II CHEMISTRY SYSTEM

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS·Product code JJE·November 25, 2013

    VITROS CHEMISTRY PRODUCTS CKMB SLIDES

    FDA Adverse Event
    Malfunction ·Product code JHS·August 22, 2018

    VITROS CHEMISTRY PRODUCTS CKMB SLIDES

    FDA Adverse Event
    Malfunction ·Product code JHS·August 22, 2018

    VITROS CHEMISTRY PRODUCTS CKMB SLIDES

    FDA Adverse Event
    Malfunction ·Product code JHS·August 22, 2018

    VITROS IMMUNODIAGNOSTIC PRODUCTS TSH REAGENT PACK

    FDA Adverse Event
    Malfunction ·ORTHO-CLINICAL DIAGNOSTICS, INC.·Product code JLW·April 10, 2023

    UNICEL DXC 600I SYNCHRON ACCESS CLINICAL SYSTEM

    FDA Adverse Event
    Malfunction ·BECKMAN COULTER, INC.·Product code JJE·December 8, 2008

    TVT EXACT RETROPUBIC SYSTEM

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTN·September 8, 2023

    GYNECARE MESH UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code FTM·May 5, 2023

    1319681-2017-00082

    FDA Adverse Event
    Malfunction ·September 25, 2017

    Fibrotek

    FDA UDI
    R 2 DIAGNOSTICS, INC.·00859394006040·Fibrinogen assay 100 DET

    LupoTek Detectin VL

    FDA UDI
    R 2 DIAGNOSTICS, INC.·10859394006108·Venom Screening test of LA 10 x 2 ml

    Phosphoplastin RL

    FDA UDI
    R 2 DIAGNOSTICS, INC.·10859394006023·PT reagent 10 x 5 ml

    T-tek

    FDA UDI
    R 2 DIAGNOSTICS, INC.·10859394006054·Thrombin Time 10 x 1 ml

    LupoTek Correctin VL

    FDA UDI
    R 2 DIAGNOSTICS, INC.·10859394006115·Venom Confirmatory test for LA 10 x 1 ml

    NoFact VIII

    FDA UDI
    R 2 DIAGNOSTICS, INC.·10859394006153·Factor VIII immunodepleted 10 x 1 ml

    PlasmaRef ARL-2

    FDA UDI
    R 2 DIAGNOSTICS, INC.·10859394006184·Assayed Reference Plasma L-2 10 x 1 ml

    NoFact IX

    FDA UDI
    R 2 DIAGNOSTICS, INC.·10859394006160·Factor IX immunodepleted 10 x 1 ml

    Phosphoplastin RL

    FDA UDI
    R 2 DIAGNOSTICS, INC.·10859394006030·PT reagent 10 x 10 ml