NEWPORT MEDICAL INSTRUMENTS INC.

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Description

5 dispositivos en la base de datos

  • Modelo / Serial
    Model Catalog: ITEM CODE 553280 (Lot serial: SN2096134110001-2292048120050)
  • Clasificación del producto
  • Descripción del producto
    Power Pac Batteries for HT70 ventilators
  • Modelo / Serial
    Model Catalog: (Lot serial: manufacturer.); Model Catalog: (Lot serial: >10 serial numbers.); Model Catalog: (Lot serial: Contact importer or)
  • Descripción del producto
    Newport e360 Ventilator
  • Modelo / Serial
    Model Catalog: HT50 (Lot serial: N/A)
  • Clasificación del producto
  • Descripción del producto
    HT50 VENTILATOR
  • Modelo / Serial
    Model Catalog: (Lot serial: ALL UNITS BEFORE 01 OCT 2004)
  • Descripción del producto
    Newport HT50 Ventilator
  • Modelo / Serial
    Model Catalog: (Lot serial: 02091107); Model Catalog: (Lot serial: 02101189); Model Catalog: (Lot serial: 02111303)
  • Descripción del producto
    HT50 VENTILATOR

2 fabricantes con un nombre similar

Más información acerca de la data acá

  • Dirección del fabricante
    NEWPORT BEACH
  • 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
    HC
  • 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
    RLMPH