EV3 INC.

6 dispositivos en la base de datos

  • Modelo / Serial
    Model Catalog: (Lot serial: )
  • Descripción del producto
    TRAP Cardiovascular and Neurovascular
  • Modelo / Serial
    Model Catalog: (Lot serial: 2681547); Model Catalog: (Lot serial: 1940695); Model Catalog: (Lot serial: 1940667)
  • Descripción del producto
    IntraStent LD Max
  • Modelo / Serial
    Model Catalog: AB14W025120150 (Lot serial: 9416365); Model Catalog: AB14W020080150 (Lot serial: 8778807); Model Catalog: AB14W020120150 (Lot serial: 9416365); Model Catalog: AB14W020080150 (Lot serial: 9416365); Model Catalog: AB14W025120150 (Lot serial: 9248597); Model Catalog: AB14W020120150 (Lot serial: 9248597); Model Catalog: AB14W020080150 (Lot serial: 9248597); Model Catalog: AB14W025120150 (Lot serial: 8815410); Model Catalog: AB14W020120150 (Lot serial: 8815410); Model Catalog: AB14W020080150 (Lot serial: 8815410); Model Catalog: AB14W025120150 (Lot serial: 8811586); Model Catalog: AB14W020120150 (Lot serial: 8811586); Model Catalog: AB14W020080150 (Lot serial: 8811586); Model Catalog: AB14W025120150 (Lot serial: 8784857); Model Catalog: AB14W020120150 (Lot serial: 8784857); Model Catalog: AB14W020080150 (Lot serial: 8784857); Model Catalog: AB14W025120150 (Lot serial: 8778807); Model Catalog: AB14W020120150 (Lot serial: 8778807)
  • Clasificación del producto
  • Descripción del producto
    NANOCROSS .014" OTW PTA DILATION CATHETER
  • Modelo / Serial
    Model Catalog: XR-CS1200-55 (Lot serial: SN 1343045); Model Catalog: XR-CS1150-45 (Lot serial: SN 1343045); Model Catalog: XR-CS1200-55 (Lot serial: SN 1343019); Model Catalog: XR-CS1150-45 (Lot serial: SN 1343019); Model Catalog: XR-CS1200-55 (Lot serial: SN 1326974); Model Catalog: XR-CS1150-45 (Lot serial: SN 1326974); Model Catalog: XR-CS1150-45 (Lot serial: SN 1364082); Model Catalog: XR-CS1150-45 (Lot serial: SN 1342882); Model Catalog: XR-CS1200-55 (Lot serial: SN 1342882); Model Catalog: XR-CS1150-45 (Lot serial: SN 1342957); Model Catalog: XR-CS1200-55 (Lot serial: SN 1342957); Model Catalog: XR-CS1200-55 (Lot serial: SN 1364082)
  • Descripción del producto
    X-Sizer Catheter System
  • Modelo / Serial
    Model Catalog: XR-CS1200-55 (Lot serial: 407855)
  • Descripción del producto
    X-Sizer Catheter System
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6 fabricantes con un nombre similar

Más información acerca de la data acá

  • 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
    FSSH
  • 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
    BAM
  • 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
    BAM
  • 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
    ANVSANVISA
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