BEUDAMED
    11 results · 27ms · Sources: EU EUDAMED, US FDA

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    Filters FDA Adverse Event ×

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·May 10, 2006

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·February 1, 2006

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·September 30, 2021

    INRATIO

    FDA Adverse Event
    Malfunction ·HEMOSENSE, INC.·Product code JPA·February 1, 2006

    T:SLIM X2 INSULIN PUMP WITH CONTROL-IQ TECHNOLOGY

    FDA Adverse Event
    Malfunction ·TANDEM DIABETES CARE·Product code QFG·June 7, 2021

    INRATIO

    FDA Adverse Event
    Injury ·HEMOSENSE, INC.·Product code GIS·February 6, 2006

    INRATIO

    FDA Adverse Event
    Injury ·HEMOSENSE, INC.·Product code GIS·February 6, 2006

    T:SLIM X2 INSULIN PUMP

    FDA Adverse Event
    Injury ·TANDEM DIABETES CARE·Product code OYC·November 20, 2019

    CLAY ADAMS RUBBER CANTOR TUBE, PEDIATRIC SIZE, 12FR

    FDA Adverse Event
    Malfunction ·BECTON DICKINSON·Product code FEF·November 10, 1999

    MINICAP PD TRANSFER SET WITH TWIST CLAMP-EXTRA SHORT

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code KDJ·February 16, 1998

    SENTECH

    FDA Adverse Event
    Death ·SENTECH MEDICAL SYSTEMS, INC.·Product code FNM·August 28, 2001