Medtronic Limited

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Description

5 dispositivos en la base de datos

  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Medtronic Single Chamber Temporary External Pacemaker 53401
  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Medtronic MiniMed Silhouette and MiniMed Sure-T infusion sets
  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: [10 Oct 2013] Medtronic Model 8870 Software Application Card used in the 8840 N’Vision Clinician Programmer
  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Medtronic SynchroMed Implantable Infusion Pump
  • Modelo / Serial
  • Descripción del producto
    Medical Device Safety Alert: Medtronic Screw Module used with the ATLANTIS and Premier Anterior Cervical Plate System

2 fabricantes con un nombre similar

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
    HPRA
  • 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.
  • Representante del fabricante
    Tamer frères S.A.L.
  • Source
    RLMPH