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

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    Filters Regulation: Us FDA ×

    VenaCure EVLT NeverTouch Procedure Kits; VenaCure EVLT NeverTouch Direct Procedure Kits

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

    TIBIAL NAIL, STANDARD T2 TIBIA 9X300 MM

    FDA Adverse Event
    Injury ·STRYKER OSTEOSYNTHESIS KIEL·Product code HSB·October 12, 2012

    GE DATEX-OHMEDA AVANCE CS2

    FDA 510(k)
    FDA Class 2 ·Anesthesiology

    ARTHREX TRIMIT SCREW, MODEL AR-4161B

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    INTERMATE

    FDA Adverse Event
    Malfunction ·BAXTER HEALTHCARE - IRVINE·Product code FRN·September 1, 2011

    HUGS

    FDA Adverse Event
    Malfunction ·STANLEY SECURITY SOLUTIONS, INC.·Product code ILQ·October 17, 2014

    GORE PRECLUDE DURA SUBSTITUTE

    FDA Adverse Event
    Injury ·W. L. GORE ASSOCIATES·Product code GXQ·July 3, 2013