Bryan Cervical Disc System

Fabricant

  • 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
    SATP

3 dispositifs médicaux avec un nom similaire

En savoir plus sur les données ici

  • Modèle / numéro de série
  • Dispositif implanté ?
    Yes
  • Description du dispositif
    Non-active implants
  • Manufacturer
  • Modèle / numéro de série
    Model Catalog: 6470118 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 6470117 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 6470114 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 6470116 (Lot serial: >10 NUMBERS CONTACT MFR); Model Catalog: 6470115 (Lot serial: >10 NUMBERS CONTACT MFR)
  • Description du dispositif
    BRYAN CERVICAL DISK SYSTEM
  • Manufacturer
  • Modèle / numéro de série
  • Description du dispositif
    BRYAN Cervical Disc System
  • Manufacturer