Physio-Control Inc.

5 dispositivos en la base de datos

  • Modelo / Serial
  • Descripción del producto
    Medical electronics / Electromedical devices - electrotherapy
  • Modelo / Serial
  • Descripción del producto
    Medical electronics / Electromedical devices - electrotherapy
  • Modelo / Serial
  • Descripción del producto
    Medical electronics / Electromedical devices - electrotherapy
  • Modelo / Serial
  • Descripción del producto
    Medical electronics / Electromedical devices - electrotherapy
  • Modelo / Serial
  • Descripción del producto
    Medical electronics / Electromedical devices - electrotherapy

10 fabricantes con un nombre similar

Más información acerca de la data acá

  • Empresa matriz del fabricante (2017)
  • Source
    AEMPSVFOI
  • Empresa matriz del fabricante (2017)
  • Representante del fabricante
    Al-Jeel Medical & Trading Co. LTD
  • Source
    SFDA
  • Empresa matriz del fabricante (2017)
  • Source
    BAM
  • Empresa matriz del fabricante (2017)
  • Source
    DH
  • 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
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