BEUDAMED
    42 results · 28ms · Sources: EU EUDAMED, US FDA

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    Filters Regulation: Us FDA ×

    Healix™ Compression Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    COLONOSCOPY ASSISTANT

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

    ORTHOPEDIATRICS BONE SCREWS

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    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

    BD BBL¿ COAGULASE PLASMA, RABBIT WITH EDTA

    FDA Adverse Event
    Malfunction ·LEE LABORATORIES, INC.·Product code JTL·December 1, 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