Trevo XP Provue System

Fabricante

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    Note published by the authorities from the Netherlands: This message is a warning from the manufacturer. After placing a medical device on the market, the manufacturer is obliged to follow the device and, where necessary, to improve it. When there is a risk for the user, the manufacturer must take action. The manufacturer informs users and the inspection of this action with a warning (Field Safety Notice). See also medical device warnings. This is part of the supervision of medical technology.
  • Source
    IGJ

4 dispositivos con un nombre similar

Más información acerca de la data acá

  • Modelo / Serial
    UPN/Model No. 80052; Lot 63034
  • Clasificación del producto
  • Clase de dispositivo
    2
  • ¿Implante?
    No
  • Distribución
    OUS only - NL, FR, IT, DE, BE
  • Descripción del producto
    Trevo XP ProVue System kit containing 1) Trevo XP ProVue Retriever, 4x20mm and 2) Trevo Pro18 Microcatheter
  • Manufacturer
  • Modelo / Serial
  • Descripción del producto
    Injections / Infusions / Transfusions / Dialysis - catheters
  • Manufacturer
  • Modelo / Serial
  • Descripción del producto
    Trevo XP Provue System, TREVO XP PROVUE RETRIEVER 4X20 + TREVO PRO 18 MC KIT, Concentric Medical Inc
  • Manufacturer