BEUDAMED
    3,847 results · 42ms · Sources: EU EUDAMED, US FDA

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    Integra®

    FDA UDI
    INTEGRA LIFESCIENCES CORPORATION·10381780252320·Integra® Head Ring Drive

    HRD 645

    FDA UDI
    Ellipse A/S·05713530000352·

    HRD 645

    FDA UDI
    Ellipse A/S·05713530000079·

    REBOUND HRD

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

    MODIFICATION TO REBOUND HRD

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

    Applicator HRD 645 645 - 950 nm

    FDA UDI
    Candela Corporation·00817495023366·

    REBOUND HRD

    FDA Adverse Event
    Malfunction ·ARB MEDICAL, LLC·Product code FTL·November 1, 2018

    REBOUND HRD

    FDA Adverse Event
    Malfunction ·ARB MEDICAL, LLC·Product code FTL·November 1, 2018

    3005770977-2018-00007

    FDA Adverse Event
    Malfunction ·November 1, 2018

    REBOUND HRD

    FDA Adverse Event
    Malfunction ·ARB MEDICAL, LLC·Product code FTL·June 26, 2018

    REBOUND HRD

    FDA Adverse Event
    Injury ·ARB MEDICAL, LLC·Product code FTL·February 8, 2018

    REBOUND HRD

    FDA Adverse Event
    Injury ·ARB MEDICAL, LLC·Product code FTL·February 8, 2018

    REBOUND HRD

    FDA Adverse Event
    Malfunction ·ARB MEDICAL, LLC·Product code FTL·December 20, 2017

    REBOUND HRD

    FDA Adverse Event
    Injury ·ARB MEDICAL, LLC·Product code FTL·December 15, 2017

    REBOUND HRD

    FDA Adverse Event
    Malfunction ·MINNESOTA MEDICAL DEVELOPMENT, INC.·Product code FTL·May 16, 2011

    REBOUND HRD-V

    FDA Adverse Event
    Injury ·ARB MEDICAL, LLC·Product code FTL·March 8, 2018

    REBOUND HRD

    FDA Adverse Event
    Injury ·ARB MEDICAL, LLC·Product code FTL·February 8, 2018

    REBOUND HRD

    FDA Adverse Event
    Malfunction ·ARB MEDICAL, LLC·Product code FTL·December 30, 2016

    REBOUND HRD

    FDA Adverse Event
    Injury ·ARB MEDICAL, LLC·Product code FTL·December 20, 2017

    REBOUND HRD

    FDA Adverse Event
    Injury ·ARB MEDICAL, LLC·Product code FTL·December 20, 2017