BEUDAMED
    7 results · 18ms · Sources: EU EUDAMED, US FDA

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    ACE CANCELLOUS BONE SCREW

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    AMSELF CLOSED CATHETERIZATION SYSTEM

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

    SabreLine and SabreGuard Laser Fibers

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

    OPTETRAK

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·May 25, 2023

    LIGAMAX-5MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code FZP·October 26, 2010

    IDRIVE ULTRA POWERED HANDLE 1

    FDA Adverse Event
    Malfunction ·COVIDIEN LP,·Product code GDW·February 20, 2014

    PENUMBRA COIL 400

    FDA Adverse Event
    Malfunction ·PENUMBRA, INC.·Product code HCG·December 20, 2012