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

    Get notified when this changes

    We'll email you when new records match this search — new devices, new clearances, certificate changes, or withdrawals.
    Filters Regulation: Us FDA ×

    Over-tube (TR-1108A)

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

    NA

    FDA UDI
    Synthes GmbH·10886982168962·2.0MM STRAIGHT PLATE 12 HOLES

    WaveForm™ C

    FDA UDI
    Seaspine Orthopedics Corporation·10889981220051·Interbody, 14x13x9mm, 10 Degree, 3D

    Surgisleeve Wound Protector

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

    NAVIGUS NEXDRIVE, MODEL MI-3000

    FDA 510(k)
    FDA Class 2 ·Neurology

    CUI TEXTURED SILICONE GEL FILLED BREAST IMPLANT

    FDA Adverse Event
    Injury ·ALLERGAN (COSTA RICA)·Product code FTR·July 5, 2024

    HUT EXT DR FINAL ASSY-REVERSE

    FDA Adverse Event
    Malfunction ·LIEBEL-FLARSHEIM CO.·Product code KQS·November 21, 2008

    CURRENT RF DR

    FDA Adverse Event
    Death ·ST JUDE MEDICAL CARDIAC RHYTHM MANAGEMENT DIVISION·Product code LWS·September 11, 2011

    HUDSON SHERIDAN/CF MAGILL TRACHEAL TUBE, 9.0MM

    FDA Adverse Event
    Malfunction ·TELEFLEX MEDICAL·Product code BTR·July 18, 2013