BEUDAMED
    11 results · 20ms · Sources: EU EUDAMED, US FDA

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    ASEPTIC TRANSFER SET

    FDA 510(k)
    FDA Class 2 ·General Hospital

    Archon

    FDA UDI
    Nuvasive, Inc.·00887517200334·Archon Screw, 4.0x17mm Self-Tap Var

    SurgyNeedle

    FDA UDI
    U.S. SURGITECH INC.·00810014630274·

    NA

    FDA UDI
    Zimmer, Inc.·00889024133969·

    NA

    FDA UDI
    Zimmer, Inc.·00889024133952·

    LEE-FILL ULTRAVIOLET-CURED REST. MAT.

    FDA 510(k)
    FDA Class 2 ·Dental

    Self-destruction Safety Syringes for Single Use; Sterile Hypodermic Syringes for Single Use; Sterile Hypodermic Needles for Single Use; Sterile Safety Hypodermic Needles for Single Use

    FDA 510(k)
    FDA Class 2 ·General Hospital

    SPECTRUM INFUSON PUMP

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE CORP·Product code FRN·January 3, 2014

    FINELINE II

    FDA Adverse Event
    Injury ·CPI - DEL CARIBE·Product code NVN·October 10, 2012

    FREESTYLE FLASH

    FDA Adverse Event
    Malfunction ·ABBOTT DIABETES CARE INC, USA·Product code LFR·July 16, 2007

    MENTOR MEMORYGEL BREAST IMPLANT

    FDA Adverse Event
    Injury ·MENTOR TEXAS·Product code FTR·September 24, 2025