BEUDAMED
    1,901 results · 33ms · Sources: EU EUDAMED, US FDA

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    TRIAGE METER PRO

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code KHO·April 13, 2017

    KIT, TRIAGE, CARDIAC TNI

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code GJS·November 18, 2014

    KIT, TRIAGE, CARDIAC TNI / CKMB

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code MMI·May 20, 2013

    KIT, TRIAGE, CARDIAC TNI/ CKMB

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code MMI·May 20, 2013

    TRIAGE CARDIAC PANEL 25 TEST

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code NBC·August 25, 2014

    TRIAGE CARDIAC TRIPLE MARKER PANEL

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code NBC·November 22, 2016

    TRIAGE CARDIAC TRIPLE MARKER PANEL

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code NBC·November 22, 2016

    TRIAGE CARDIAC PROFILER KIT

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code MMI·March 7, 2012

    TRIAGE CARDIAC HS TNI PANEL

    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·March 27, 2021

    TRIAGE D-DIMER PANEL

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·November 9, 2015

    VITEK 2 AST-GP75 TEST KIT

    FDA Adverse Event
    Malfunction ·BIOMÉRIEUX, INC.·Product code LON·September 10, 2020

    2027969-2015-00668

    FDA Adverse Event
    Malfunction ·September 11, 2015

    ORTHO REAGENT RED BLOOD CELLS 0.8% SELECTOGEN

    FDA Adverse Event
    Malfunction ·ORTHO CLINICAL DIAGNOSTICS·Product code QHT·June 5, 2020

    ORTHO REAGENT RED BLOOD CELLS 0.8% SELECTOGEN

    FDA Adverse Event
    Malfunction ·ORTHO CLINICAL DIAGNOSTICS·Product code QHT·June 5, 2020

    HAEMOLANCE PLUS MAX FLOW

    FDA Adverse Event
    Injury ·HTL-STREFA S.A.·Product code FMK·September 21, 2016

    EVERSENSE SENSOR

    FDA Adverse Event
    Malfunction ·SENSEONICS INC.·Product code QCD·May 13, 2021

    EVERSENSE SENSOR

    FDA Adverse Event
    Malfunction ·SENSEONICS INC.·Product code QCD·April 16, 2021

    EVERSENSE SENSOR

    FDA Adverse Event
    Malfunction ·SENSEONICS INC.·Product code QCD·April 6, 2021

    EVERSENSE SENSOR

    FDA Adverse Event
    Malfunction ·SENSEONICS INC.·Product code QCD·June 13, 2021

    EVERSENSE TRANSMITTER

    FDA Adverse Event
    Injury ·SENSEONICS INC.·Product code QCD·May 4, 2021