BEUDAMED
    8 results · 23ms · 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 ×

    PUNCH SURGICAL

    FDA 510(k)
    FDA Class 1 ·Orthopedic

    Ventura NanoMetalene System

    FDA UDI
    Seaspine Orthopedics Corporation·10889981152239·Ventura NM Trial, 11mm x 32mm x 11mm, Lordotic

    SHIRAZ-JAVA SPINAL FIXATION SYSTEM

    FDA 510(k)
    FDA Class 2 ·Orthopedic

    Disposable Dual Action Tissue Closure Device

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

    TRULIANT TIB IMP CRC INSERT SZ 4, 13MM

    FDA Adverse Event
    Injury ·EXACTECH, INC.·Product code JWH·April 22, 2024

    ENCOR BREAST BIOPSY PROBE

    FDA Adverse Event
    Malfunction ·BARD PERIPHERAL VASCULAR, INC.·Product code KNW·April 3, 2014

    XIENCE V EVEROLIMUS ELUTING CORONARY STENT SYSTEM

    FDA Adverse Event
    Injury ·AV-TEMECULA-CT·Product code NIQ·January 29, 2013

    PROXIMATE** RELOADABLE VASCULAR LINEAR STAPLER - 30 MM

    FDA Adverse Event
    Malfunction ·ETHICON ENDO-SURGERY, LLC.·Product code GDW·December 21, 2010