Covidien || Newport Medical Instruments, Inc. || Mallinckrodt Medical || Covidien Llc

  • 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
    NIDFSINVIMA
  • 3 Events

3 dispositifs dans la base de données

  • Modèle / numéro de série
    760 and 840
  • Description du dispositif
    Deliver gases to the respiratory tract to assist or supply basic needs in physiological and respiratory conditions required by the patient.
  • Modèle / numéro de série
    PURITAN BENNETT 980
  • Description du dispositif
    Deliver gases to the respiratory tract to assist or supply the basic needs in physiological and respiratory conditions required by the patient.
  • Modèle / numéro de série
    840
  • Classification du dispositif
  • Description du dispositif
    Deliver gases to the respiratory tract to assist or supply basic needs in physiological and respiratory conditions required by the patient.

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