BIO-CONSOLE DRIVE UNIT (550)

  • Modèle / numéro de série
    Model Catalog: 95208 (Lot serial: 8729 8622); Model Catalog: 95208 (Lot serial: S/N'S 8473 8466 8687 8607); Model Catalog: 95208 (Lot serial: 8184 8677); Model Catalog: ATLG110 (Lot serial: MANUFACTURER); Model Catalog: ATLG110 (Lot serial: CONTACT); Model Catalog: ATLG110 (Lot serial: >10 NUMBERS); Model Catalog: MAG100 (Lot serial: MAG1000594); Model Catalog: MAG100 (Lot serial: MAG1000019 MAG1000597); Model Catalog: MAG100 (Lot serial: MAG1000249 MAG1000644); Model Catalog: MAG100 (Lot serial: MAG1000043 MAG1000506); Model Catalog: MAG100 (Lot serial: S/N'S MAG1001017 MAG1000592); Model Catalog: 560 (Lot serial: MANUFACTURER); Model Catalog: 560 (Lot serial: >10 NUMBERS); Model Catalog: 560 (Lot serial: CONTACT)
  • Description du dispositif
    BIO-CONSOLE DRIVE UNIT (550)
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    BRAMPTON
  • 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
    HC