NEWPORT MEDICAL INSTRUMENTS INC.

  • Adresse du fabricant
    COSTA MESA
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “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
  • 5 Events

5 dispositifs dans la base de données

  • Modèle / numéro de série
    Model Catalog: ITEM CODE 553280 (Lot serial: SN2096134110001-2292048120050)
  • Classification du dispositif
  • Description du dispositif
    Power Pac Batteries for HT70 ventilators
  • Modèle / numéro de série
    Model Catalog: (Lot serial: manufacturer.); Model Catalog: (Lot serial: >10 serial numbers.); Model Catalog: (Lot serial: Contact importer or)
  • Description du dispositif
    Newport e360 Ventilator
  • Modèle / numéro de série
    Model Catalog: HT50 (Lot serial: N/A)
  • Classification du dispositif
  • Description du dispositif
    HT50 VENTILATOR
  • Modèle / numéro de série
    Model Catalog: (Lot serial: ALL UNITS BEFORE 01 OCT 2004)
  • Description du dispositif
    Newport HT50 Ventilator
  • Modèle / numéro de série
    Model Catalog: (Lot serial: 02091107); Model Catalog: (Lot serial: 02101189); Model Catalog: (Lot serial: 02111303)
  • Description du dispositif
    HT50 VENTILATOR

2 fabricants avec un nom similaire

En savoir plus sur les données ici

  • Adresse du fabricant
    NEWPORT BEACH
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “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
  • Société-mère du fabricant (2017)
  • Commentaire du fabricant
    “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