United States Surgical

6 dispositifs dans la base de données

  • Modèle / numéro de série
    Lot Numbers: N5L338, N5M232, N6B266, N6C11
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide and International Australia, Brazil, Panama City, Singapore, Chile, France, Germany, Israel, Argentina, Quebec
  • Description du dispositif
    Auto Suture ChemoSite Implantable Venous Access System with 9FR Introducer Kit with Silicone Catheter || Catalog Number: 120066
  • Modèle / numéro de série
    Lot Number:  N5M255
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide and International Australia, Brazil, Panama City, Singapore, Chile, France, Germany, Israel, Argentina, Quebec
  • Description du dispositif
    Auto Suture ChemoSite Catheter Introducer Kit with 9FR Peel-Away Sheath || Catalog Number: 120049
  • Modèle / numéro de série
    Lot Numbers: N5M90, N6A546, N6B147, N6B351, N6C127, N6C331
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide and International Australia, Brazil, Panama City, Singapore, Chile, France, Germany, Israel, Argentina, Quebec
  • Description du dispositif
    Auto Suture ChemoSite Implantablei Venous Kit Access System with 9FR Introducer Kit Catalog Number: 120045
  • Modèle / numéro de série
    Lot Numbers: N5L380, N5M159, N6B02,N6B45
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide and International Australia, Brazil, Panama City, Singapore, Chile, France, Germany, Israel, Argentina, Quebec
  • Description du dispositif
    Auto Suture ChemoSite Catheter 9FR Introducer Kit with 9FR Peel-Away Sheath || Catalog Number: 120039
  • Modèle / numéro de série
    Lot Numbers: N5M160, N6B268
  • Classification du dispositif
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide and International Australia, Brazil, Panama City, Singapore, Chile, France, Germany, Israel, Argentina, Quebec
  • Description du dispositif
    Auto Suture ChemoSite Low Profile Venous Access System with 9FR Introducer Kit with Silicone Catheter || Catalog Number: 120025
1 de plus

7 fabricants avec un nom similaire

En savoir plus sur les données ici

  • Adresse du fabricant
    United States Surgical, 195 Mcdermott Rd, North Haven CT 06473-3665
  • Source
    USFDA
  • Adresse du fabricant
    United States Surgical Corporation, 195 Mcdermott Rd, North Haven CT 06473-3665
  • Source
    USFDA
  • 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
    VNSAWH
  • 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
    VNSAWH
  • 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
2 en plus