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

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    Filters FDA Adverse Event ×

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Malfunction ·UNOMEDICAL UM-D·Product code FPA·March 13, 2025

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Malfunction ·UNOMEDICAL UM-D·Product code FPA·March 13, 2025

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Malfunction ·UNOMEDICAL UM-D·Product code FPA·March 13, 2025

    MONOJET SYRINGE

    FDA Adverse Event
    Malfunction ·SHERWOOD MEDICAL CO.·Product code FMF·April 25, 1994

    MONOJET SYRINGE

    FDA Adverse Event
    Malfunction ·SHERWOOD MEDICAL CO.·Product code FMF·April 25, 1994

    ACCU-CHEK FLEXLINK

    FDA Adverse Event
    Malfunction ·UNOMEDICAL UM-D·Product code FPA·March 13, 2025

    NV GXL LINR, NTRL, 36MM ID, GROUP 3 CUPS

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JDI·August 29, 2024

    ACROBAT SUV OFF PUMP SYS, W/XP4000 STD

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code DXC·March 11, 2013

    ONE TOUCH PING GLUCOSE MANAGEMENT SYSTEM

    FDA Adverse Event
    Injury ·ANIMAS CORPORATION·Product code LZG·February 22, 2011

    SYNCHROMED II

    FDA Adverse Event
    Malfunction ·MEDTRONIC NEUROMODULATION·Product code LKK·February 15, 2008