BEUDAMED
    15 results · 21ms · Sources: EU EUDAMED, US FDA

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    LORENZ STENT

    FDA 510(k)
    FDA Class 2 ·Ear, Nose, Throat

    DeRoyal

    FDA UDI
    DEROYAL INDUSTRIES, INC.·00749756687188·PLASTIC HAND PACK

    EVERGOOD BRAND (PATIENT EXAM GLOVES-LATEX)

    FDA 510(k)
    FDA Class 1 ·General Hospital

    RUBBER DAM

    FDA 510(k)
    FDA Class 1 ·Dental

    9900

    FDA Adverse Event
    Malfunction ·GE OEC MEDICAL SYSTEMS (SLC)·Product code JAA·May 19, 2014

    QUICKFLEX MICRO LV LEAD

    FDA Adverse Event
    Injury ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code NIK·November 10, 2010

    VASO VIEW HEMOPRO

    FDA Adverse Event
    Malfunction ·MAQUET CARDIOVASCULAR, LLC·Product code GEI·December 28, 2012

    GORE VIABAHN® ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·June 15, 2016

    GORE VIABAHN® ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·June 15, 2016

    GORE VIABAHN® ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·June 15, 2016

    GORE VIABAHN® ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·June 15, 2016

    GORE VIABAHN® ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·June 15, 2016

    GORE VIABAHN® ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·June 15, 2016

    GORE VIABAHN® ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·June 15, 2016

    GORE VIABAHN® ENDOPROSTHESIS

    FDA Adverse Event
    Injury ·W.L. GORE & ASSOCIATES·Product code NIP·June 15, 2016