SynchroMed® II Implantable Drug Pumps

Manufacturer

  • Manufacturer Parent Company (2017)
  • Manufacturer comment
    “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
    DMA

7 devices with a similar name

Learn more about the data here

  • Model / Serial
    Model Number: 8637-20, 8637-40 Serial Number: Všechna
  • Product Description
    Active implantable medical devices
  • Manufacturer
  • Model / Serial
    Model Number: 8637-20, 8637-40 Serial Number: Všechny pumpy vyrobené od března 2015 do prosince 2010 a pumpy vyrobené s předchozí konstrukcí baterie od ledna 2011 do června 2011. Batch Number: všechna
  • Product Description
    Active implantable medical devices
  • Manufacturer
  • Model / Serial
    Model Number: 8637-20, 8637-40 Serial Number: Všechny pumpy s datem použitelnosti do 31.12.2018 vyrobené před konstrukční změnou.
  • Product Description
    Active implantable medical devices
  • Manufacturer
  • Model / Serial
  • Product Description
    Medtronic: SynchroMed® II implantable drug pumps
  • Manufacturer
  • Model / Serial
  • Product Description
    Medtronic: SynchroMed® II Implantable Drug Pumps
  • Manufacturer
2 more