BEUDAMED
    9 results · 45ms · Sources: EU EUDAMED, US FDA

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    Filters Status: Malfunction ×

    HEMOCHRON WHOLE BLOOD MICROCOAGULATION SYSTEM - ACT-LR CUVETTES

    FDA Adverse Event
    Malfunction ·ACCRIVA DIAGNOSTICS, INC.·Product code JBP·November 4, 2025

    HEMOCHRON¿ WHOLE BLOOD MICROCOAGULATION SYSTEM-HEMOCHRON SIGNATURE ELITE INSTR

    FDA Adverse Event
    Malfunction ·ACCRIVA DIAGNOSTICS, INC.·Product code JPA·October 3, 2025

    HEMOCHRON SIGNATURE ELITE

    FDA Adverse Event
    Malfunction ·ACCRIVA DIAGNOSTICS, INC./WERFEN·Product code JPA·April 23, 2025

    HEMOCHRON SIGNATURE ELITE WHOLE BLOOD MICROCOAGULATION SYSTEM

    FDA Adverse Event
    Malfunction ·ACCRIVA DIAGNOSTICS HOLDINGS, INC.·Product code JPA·May 1, 2020

    AVOXIMETER WHOLE BLOOD OXIMETER

    FDA Adverse Event
    Malfunction ·ACCRIVA DIAGNOSTICS HOLDINGS, INC.·Product code DQA·April 20, 2020

    AVOXIMETER WHOLE BLOOD OXIMETER

    FDA Adverse Event
    Malfunction ·ACCRIVA DIAGNOSTICS HOLDINGS, INC.·Product code DQA·May 2, 2019

    HEMOCHRON SIGNATURE ELITE

    FDA Adverse Event
    Malfunction ·WERFEN, S.A. / ACCRIVA DIAGNOSTICS, INC.·Product code JPA·November 12, 2025

    HEMOCHRON

    FDA Adverse Event
    Malfunction ·ACCRIVA DIAGNOSTICS INC., DBA ITC, DBA ACCUMETRICS·Product code JPA·September 18, 2015

    HEMOCHRON SIGNATURE ELITE

    FDA Adverse Event
    Malfunction ·ACCRIVA DIAGNOSTIC INC., DBA INC, DBA ACCUMETRICS·Product code JPA·February 12, 2018