United States Surgical

6 devices in the database

  • Model / Serial
    Lot Numbers: N5L338, N5M232, N6B266, N6C11
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide and International Australia, Brazil, Panama City, Singapore, Chile, France, Germany, Israel, Argentina, Quebec
  • Product Description
    Auto Suture ChemoSite Implantable Venous Access System with 9FR Introducer Kit with Silicone Catheter || Catalog Number: 120066
  • Model / Serial
    Lot Number:  N5M255
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide and International Australia, Brazil, Panama City, Singapore, Chile, France, Germany, Israel, Argentina, Quebec
  • Product Description
    Auto Suture ChemoSite Catheter Introducer Kit with 9FR Peel-Away Sheath || Catalog Number: 120049
  • Model / Serial
    Lot Numbers: N5M90, N6A546, N6B147, N6B351, N6C127, N6C331
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide and International Australia, Brazil, Panama City, Singapore, Chile, France, Germany, Israel, Argentina, Quebec
  • Product Description
    Auto Suture ChemoSite Implantablei Venous Kit Access System with 9FR Introducer Kit Catalog Number: 120045
  • Model / Serial
    Lot Numbers: N5L380, N5M159, N6B02,N6B45
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide and International Australia, Brazil, Panama City, Singapore, Chile, France, Germany, Israel, Argentina, Quebec
  • Product Description
    Auto Suture ChemoSite Catheter 9FR Introducer Kit with 9FR Peel-Away Sheath || Catalog Number: 120039
  • Model / Serial
    Lot Numbers: N5M160, N6B268
  • Product Classification
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide and International Australia, Brazil, Panama City, Singapore, Chile, France, Germany, Israel, Argentina, Quebec
  • Product Description
    Auto Suture ChemoSite Low Profile Venous Access System with 9FR Introducer Kit with Silicone Catheter || Catalog Number: 120025
One more

7 manufacturers with a similar name

Learn more about the data here

  • Manufacturer Address
    United States Surgical, 195 Mcdermott Rd, North Haven CT 06473-3665
  • Source
    USFDA
  • Manufacturer Address
    United States Surgical Corporation, 195 Mcdermott Rd, North Haven CT 06473-3665
  • Source
    USFDA
  • 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
    VNSAWH
  • 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
    VNSAWH
  • 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
    SATP
2 more