BEUDAMED
    7 results · 19ms · Sources: EU EUDAMED, US FDA

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    DIAMOND'S MEDIUM MODIFIED

    FDA 510(k)
    FDA Class 1 ·Microbiology

    STRYKER VISION ELECT WHDTV (STRYKER VE WHDTV)

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

    Chiral Surgical Pedicle Screw System

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    DAILY ACTIVITY ASSIST DEVICES

    FDA Adverse Event
    Malfunction ·INVAMEX·Product code ILS·June 18, 2014

    ACCU-CHEK ® MULTICLIX

    FDA Adverse Event
    Malfunction ·ROCHE DIAGNOSTICS·Product code FMK·October 25, 2010

    MONOPOLAR CAUTERY INSTRUMENT

    FDA Adverse Event
    Malfunction ·INTUITIVE SURGICAL,INC.·Product code NAY·December 20, 2012

    SPRYSTEP VECTOR, Custom made device dynamic ankle-foot orthosis (AFO) , Reference numbers: 17V1030, 17V2030, 17V1031, 17V2031, 17V1032, 17V2032, 17V1033, 17V2033, 17V1035, 17V2035, 17V1036, 17V2036, 17V1037, 17V2037

    FDA Enforcement
    Class II ·Completed·Townsend Design·January 17, 2024