Device Recall EKOS EkoSonic Endovascular System

  • Modelo / Serial
    CIC Serial Numbers:  19598-095, 19598-097, 19598-099, 19598-100, 19598-102, 19598-103,  19598-106, 19598-107, 19598-108, 19598-110, 19598-111, 19598-112,  19598-113, 19598-114, 19598-115, 19598-116, 19598-117, 19598-118,  19598-119, 19598-120, 19598-122, 19598-125, 19598-126, 19598-127,  19598-128, 19598-130, 19598-131, 19598-132, 19598-133, 19598-135,  19598-136, 19598-139, 19598-140, 19598-141, 19598-143, 19598-144,  19598-145, 19598-146, 19598-147, 19598-151, 19598-152, 19598-153,  19598-154, 19598-156, 19598-157, 19598-158.
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    Nationwide Distribution
  • Descripción del producto
    The EKOS EkoSonic Control Unit is intended exclusively for use with the EkoSonic Endovascular Device and the EkoSonic MACH4 Endovascular Device. || The EkoSonic Endovascular System consists of three main components: || -a single use EkoSonic Endovascular Device which is comprised of an Intelligent Drug Delivery Catheter (IDDC) and || -removable MicroSonic Device (MSD), and || -a reusable EKOS EkoSonic Control System. || During use, fluids are delivered through the side-holes of the IDDC. The MSD is placed through the central lumen of the IDDC to deliver ultrasound energy along the length of fluid delivery, dispersing the fluid into the intravascular treatment site. || The reusable EKOS EkoSonic Control Unit provides power to the system and the user interface for operator control. || A reusable, nonsterile Connector Interface Cable connects the EKOS EkoSonic Control Unit to the EkoSonic Endovascular Device.
  • Manufacturer
  • 1 Event

Fabricante

  • Dirección del fabricante
    EKOS Corporation, 11911 N Creek Pkwy S, Bothell WA 98011-8809
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA