Cryocath Technologies Inc.

  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “If our surveillance systems identify a potential performance issue, our personnel promptly evaluate the problem, including, when appropriate, conducting root cause investigations and internal testing to assess whether the product continues to meet specifications and defined performance criteria,” Medtronic told ICIJ in a statement. “In some cases, based on this evaluation, Medtronic may determine that a recall is necessary.” The company said that it communicates with healthcare providers and/or patients and provide recommendations to address such issues. Medtronic noted that these communications can include letters, emails, calls, press releases, physician notifications and social media postings, as well as informing the FDA and other regulators of the actions.
  • Source
    SATP
  • 1 Event

Un dispositivo en la base de datos

  • Modelo / Serial
    2FC12
  • Descripción del producto
    MD: Catheter, intravascular, guiding

Fabricante con un nombre similar

Más información acerca de la data acá

  • Dirección del fabricante
    CryoCath Technologies Inc., 16771 Chemin Ste-Marie, Kirkland Canada
  • Source
    USFDA