Medtronic International Limited

45 dispositifs dans la base de données

  • Modèle / numéro de série
  • Description du dispositif
    Medtronic EnVeo R Loading System
  • Modèle / numéro de série
  • Description du dispositif
    Medtronic 23mm Engager Transcatheter Aortic Bioprosthesis
  • Modèle / numéro de série
  • Description du dispositif
    NIM® Standard Reinforced EMG Endotracheal Tube, Medtronic Xomed Inc
  • Modèle / numéro de série
  • Description du dispositif
    Saw Sagittal, Saw Sagittal Refurbished, Saw Sagittal Finger & Saw Sagittal Finger Refurbished, Medtronic Xomed
  • Modèle / numéro de série
  • Description du dispositif
    Pedicle Access Kit (PAK) Needles, Medtronic Sofamor Danek USA Inc.
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  • 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
    DH