COVIDIEN LLC

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Description

27 dispositivos en la base de datos

  • Modelo / Serial
    Model Catalog: (Lot serial: CAT:8881512852)
  • Descripción del producto
    MONOJECT SYRINGE 12CC
  • Modelo / Serial
    Model Catalog: (Lot serial: Model No. 5329 SCD Blue Sleeve); Model Catalog: (Lot serial: Model No. 5330 SCD Blue Sleeve); Model Catalog: (Lot serial: Model No. 5345 SCD Blue Sleeve); Model Catalog: (Lot serial: Model No. 5480 SCD Blue Sleeve)
  • Descripción del producto
    SCD SEQUENTIAL COMPRESSION SLEEVES
  • Modelo / Serial
    Model Catalog: 3259-62 (8886325962) (Lot serial: D1C0554X); Model Catalog: 3259-62 (8886325962) (Lot serial: D1C0553X); Model Catalog: 2-0 (GS62M) (Lot serial: D1D0057GX); Model Catalog: 3-0 (GS63M) (Lot serial: D1D0057GX); Model Catalog: 3-0 (GS33M) (Lot serial: D1D0057GX); Model Catalog: 2-0 (GS62M) (Lot serial: D1C0416); Model Catalog: 3-0 (GS63M) (Lot serial: D1C0416); Model Catalog: 3-0 (GS33M) (Lot serial: D1C0416); Model Catalog: 2-0 (GS62M) (Lot serial: D1C0323g); Model Catalog: 3-0 (GS63M) (Lot serial: D1C0323g); Model Catalog: 3-0 (GS33M) (Lot serial: D1C0323g); Model Catalog: 2-0 (GS62M) (Lot serial: D1C0442G); Model Catalog: 3-0 (GS63M) (Lot serial: D1C0442G); Model Catalog: 3-0 (GS33M) (Lot serial: D1C0442G); Model Catalog: 2-0 (GS62M) (Lot serial: D1C0690GX); Model Catalog: 3-0 (GS33M) (Lot serial: D1C0690GX); Model Catalog: 3-0 (GS63M) (Lot serial: D1C0690GX)
  • Descripción del producto
    TICRON NON-ABSORBABLE POLYESTER SUTURES
  • Modelo / Serial
    Model Catalog: N-85 (Lot serial: >THAN 10 PLS CONTACT MFG)
  • Descripción del producto
    FILTERLINE H SET INFANT/NEONATAL IN N-85 MONITOR KIT
  • Modelo / Serial
    Model Catalog: RS10 (Lot serial: 161510095H); Model Catalog: RS10 (Lot serial: 162390212H); Model Catalog: RS10 (Lot serial: 162320191H); Model Catalog: RS10 (Lot serial: 162110103H); Model Catalog: RS10 (Lot serial: 161620089H); Model Catalog: RS10 (Lot serial: 161970090H); Model Catalog: RS10 (Lot serial: 161900091H); Model Catalog: RS10 (Lot serial: 161760132H); Model Catalog: RS10 (Lot serial: 161690203H); Model Catalog: RS10 (Lot serial: 162040107H)
  • Descripción del producto
    NELLCOR FOREHEAD SPO2 SENSOR
22 más

62 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
    TDMDAT
  • 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
    TDMDAT
  • 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
    NIDFSINVIMA
  • 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
    NIDFSINVIMA
  • 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
    NIDFSINVIMA
57 más