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

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    Filters Regulation: Us FDA ×

    Segmented Esophageal Stent System

    FDA 510(k)
    FDA Class 2 ·General, Plastic Surgery

    PILLING

    FDA UDI
    TELEFLEX INCORPORATED·24026704513479·

    Ophthalmic Retractor

    FDA UDI
    KATENA PRODUCTS, INC.·00841668100967·DESMARRES LID RETRACTOR #1

    General Instruments

    FDA UDI
    ALPHATEC SPINE, INC.·00840180538753·SQUARE ENDPLATE SCRAPER, UP ANGLED

    CVS SILVER BANDAGES, WALGREENS SILVER BANDAGES, XYZ SILVER BANDAGES

    FDA 510(k)
    FDA Unclassified ·Unknown

    MODEL LUNA MANUAL WHEELCHAIR

    FDA 510(k)
    FDA Class 1 ·Physical Medicine

    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