BEUDAMED
    169 results · 25ms · Sources: EU EUDAMED, US FDA

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    Surdial DX Hemodialysis System

    FDA 510(k)
    FDA Class 2 ·Gastroenterology, Urology

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    NIPRO BLOOD TUBING SET W/TP

    FDA Adverse Event
    Malfunction ·NIPRO (THAILAND) CORP. LTD.·Product code FJK·February 6, 2024

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 6, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 4, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    NIPRO BLOOD TUBING SET W/TP

    FDA Adverse Event
    Injury ·NIPRO (THAILAND) CORP. LTD.·Product code FJK·January 17, 2024

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 5, 2021

    SURDIAL X

    FDA Adverse Event
    Malfunction ·SHIBUYA (SBY)·Product code KDI·August 4, 2021