United States Surgical

4 dispositivos en la base de datos

  • Modelo / Serial
    D1B0584X, D1CO245X, D1CO292X
  • Descripción del producto
    MD: Silk suture, sterile; Suture, nylon; Polyester suture
  • Modelo / Serial
    D1B0584X, D1CO245X, D1CO292X
  • Descripción del producto
    MD: Silk suture, sterile; Suture, nylon; Polyester suture
  • Modelo / Serial
    D1B0584X, D1CO245X, D1CO292X
  • Descripción del producto
    MD: Silk suture, sterile; Suture, nylon; Polyester suture
  • Modelo / Serial
    174006 | P9H1081, P9M0112, P0B0753, P0A0021 and P0A0723
  • Descripción del producto
    MD: Surgical binding material anchor set

7 fabricantes con un nombre similar

Más información acerca de la data acá

  • Dirección del fabricante
    United States Surgical, 195 Mcdermott Rd, North Haven CT 06473-3665
  • Source
    USFDA
  • Dirección del fabricante
    United States Surgical Corporation, 195 Mcdermott Rd, North Haven CT 06473-3665
  • Source
    USFDA
  • Dirección del fabricante
    United States Surgical, 195 McDermott Rd, North Haven CT 06473-3665
  • Source
    USFDA
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “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
  • Empresa matriz del fabricante (2017)
  • Comentario del fabricante
    “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
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