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Vista de la lista Vista de las tarjetas
  • Dispositivo 8093
  • Fabricante 8093
  • Evento 8276
  • Implante 0
Carefusion Respiratory System
  • Source
    SATP
Cook Incorporated (see also under Tyco Healthcare from 03.05.2010)
  • Empresa matriz del fabricante (2017)
    Cook Group Incorporated
  • Source
    SATP
Covidien llc
  • Empresa matriz del fabricante (2017)
    Medtronic plc
  • 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
    SATP
Covidien llc
  • Empresa matriz del fabricante (2017)
    Medtronic plc
  • 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
    SATP
Datex-Ohmeda, Inc
  • Empresa matriz del fabricante (2017)
    General Electric Company
  • Source
    SATP
Datex-Ohmeda, Inc
  • Empresa matriz del fabricante (2017)
    General Electric Company
  • Source
    SATP
Dräger Medical AG & Co. KGaA
  • Empresa matriz del fabricante (2017)
    Stefan Dräger GmbH
  • Source
    SATP
Dräger Medical GmbH
  • Empresa matriz del fabricante (2017)
    Stefan Dräger GmbH
  • Source
    SATP
Drägerwerk AG & Co.KGaA
  • Empresa matriz del fabricante (2017)
    Stefan Dräger GmbH
  • Source
    SATP
Drägerwerk AG & Co.KGaA
  • Empresa matriz del fabricante (2017)
    Stefan Dräger GmbH
  • Source
    SATP
Drägerwerk AG & Co.KGaA
  • Empresa matriz del fabricante (2017)
    Stefan Dräger GmbH
  • Source
    SATP
Drägerwerk AG & Co.KGaA
  • Empresa matriz del fabricante (2017)
    Stefan Dräger GmbH
  • Source
    SATP
Drägerwerk AG & Co.KGaA
  • Empresa matriz del fabricante (2017)
    Stefan Dräger GmbH
  • Source
    SATP
Fisher& Paykel Healthcare Ltd.
  • Empresa matriz del fabricante (2017)
    Fisher & Paykel Healthcare Corporation Limited
  • Source
    SATP
GE Healthcare Clinical Systems
  • Empresa matriz del fabricante (2017)
    General Electric Company
  • Source
    SATP
GE Healthcare Clinical Systems
  • Empresa matriz del fabricante (2017)
    General Electric Company
  • Source
    SATP
GE Medical Systems Information
  • Empresa matriz del fabricante (2017)
    General Electric Company
  • Source
    SATP
GE Medical Systems Ohmeda Medical
  • Empresa matriz del fabricante (2017)
    General Electric Company
  • Source
    SATP
Halyard Health, Inc.
  • Empresa matriz del fabricante (2017)
    Halyard Health Inc
  • Source
    SATP
Hamilton Medical AG
  • Empresa matriz del fabricante (2017)
    Hamilton Bonaduz Ag
  • Source
    SATP
Hamilton Medical AG
  • Empresa matriz del fabricante (2017)
    Hamilton Bonaduz Ag
  • Source
    SATP
Inmed Manufacturing Sdn Bhd,
  • Empresa matriz del fabricante (2017)
    Teleflex Incorporated
  • Source
    SATP
Maquet Critical Care AB
  • Empresa matriz del fabricante (2017)
    Getinge AB
  • Source
    SATP
Maquet Critical Care AB
  • Empresa matriz del fabricante (2017)
    Getinge AB
  • Source
    SATP
Newport Medical Instruments, Inc.
  • Empresa matriz del fabricante (2017)
    Medtronic plc
  • 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
    SATP
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Aviso

Los dispositivos médicos ayudan con el diagnóstico, la prevención y el tratamiento de muchas lesiones y enfermedades. A través de la International Medical Devices Database no estamos sugiriendo que compañías u otras entidades mencionadas en la base de datos hayan sido parte de una conducta ilegal o hayan actuado de manera impropia. Un mismo dispositivo médico puede tener distintos nombres en diferentes países. Esta base de datos no busca proporcionar asesoría médica. Los pacientes deben consultar con sus médicos para determinar si la data contiene información relevante y si la misma tiene implicaciones médicas para ellos.

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