United States Surgical

  • 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
  • 4 Events

4 dispositifs dans la base de données

  • Modèle / numéro de série
    D1B0584X, D1CO245X, D1CO292X
  • Description du dispositif
    MD: Silk suture, sterile; Suture, nylon; Polyester suture
  • Modèle / numéro de série
    D1B0584X, D1CO245X, D1CO292X
  • Description du dispositif
    MD: Silk suture, sterile; Suture, nylon; Polyester suture
  • Modèle / numéro de série
    D1B0584X, D1CO245X, D1CO292X
  • Description du dispositif
    MD: Silk suture, sterile; Suture, nylon; Polyester suture
  • Modèle / numéro de série
    174006 | P9H1081, P9M0112, P0B0753, P0A0021 and P0A0723
  • Description du dispositif
    MD: Surgical binding material anchor set

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
  • Adresse du fabricant
    United States Surgical, 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
2 en plus