BEUDAMED
    19 results · 23ms · Sources: EU EUDAMED, US FDA

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    TRIAGE PROFILER SOB PANEL 25T

    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·July 19, 2017

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    FDA Adverse Event
    Injury ·QUIDEL CARDIOVASCULAR INC.·Product code DAP·December 13, 2019

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    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code JHX·August 29, 2017

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    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code GHH·March 4, 2021

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    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code DAP·August 3, 2018

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    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·January 25, 2017

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    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 23, 2019

    SPECTRUM INFUSION PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORPORATION·Product code FRN·January 3, 2014

    CAPSURE EPI

    FDA Adverse Event
    Injury ·MEDTRONIC, INC.·Product code DTB·October 10, 2012

    CE INTERMATE LV 250, 24 PACK,50126

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code MEB·August 3, 2010

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    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 5, 2018

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    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·January 14, 2021

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    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·October 31, 2019

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    FDA Adverse Event
    Malfunction ·ALERE SAN DIEGO, INC.·Product code DAP·February 10, 2017

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    FDA Adverse Event
    Injury ·QUIDEL CARDIOVASCULAR, INC.·Product code DAP·August 27, 2018

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    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code DAP·December 6, 2019

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    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·March 26, 2019

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    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR, INC.·Product code DAP·April 16, 2018

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    FDA Adverse Event
    Malfunction ·QUIDEL CARDIOVASCULAR INC.·Product code MMI·December 4, 2020