Medtronic International Limited

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Description

45 dispositivos en la base de datos

  • Modelo / Serial
  • Descripción del producto
    Medtronic EnVeo R Loading System
  • Modelo / Serial
  • Descripción del producto
    Medtronic 23mm Engager Transcatheter Aortic Bioprosthesis
  • Modelo / Serial
  • Descripción del producto
    NIM® Standard Reinforced EMG Endotracheal Tube, Medtronic Xomed Inc
  • Modelo / Serial
  • Descripción del producto
    Saw Sagittal, Saw Sagittal Refurbished, Saw Sagittal Finger & Saw Sagittal Finger Refurbished, Medtronic Xomed
  • Modelo / Serial
  • Descripción del producto
    Pedicle Access Kit (PAK) Needles, Medtronic Sofamor Danek USA Inc.
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Más información acerca de la data acá

  • 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
    DH