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

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    Filters Regulation: Us FDA ×

    LiftUp (Ref. Nr.: 200.56.01), LiftUp Kit (Ref. Nr.: 200.56.02)

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

    VECTOR

    FDA 510(k)
    FDA Class 2 ·Cardiovascular

    ATAC PAK BUN REAGENT

    FDA 510(k)
    FDA Class 2 ·Clinical Chemistry

    TRIDENT ACET WINDOW TRIAL 58MM

    FDA Adverse Event
    Malfunction ·STRYKER ORTHOPAEDICS-MAHWAH·Product code LXH·November 3, 2014

    PULSE GEN MODEL 103

    FDA Adverse Event
    Injury ·CYBERONICS, INC.·Product code LYJ·August 24, 2011

    UNKNOWN

    FDA Adverse Event
    Injury ·ETHICON INC.·Product code OTP·July 11, 2013