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Vista de la lista Vista de las tarjetas
  • Dispositivo 3547
  • Fabricante 3547
  • Evento 3558
  • Implante 0
Roche Diagnostics Australia Pty Limited
  • Empresa matriz del fabricante (2017)
    Roche Holding AG
  • Source
    DHTGA
LivaNova Australia Pty Ltd
  • Empresa matriz del fabricante (2017)
    LivaNova PLC
  • Source
    DHTGA
B Braun Australia Pty Ltd
  • Empresa matriz del fabricante (2017)
    Ludwig G. Braun Gmbh U. Co. Kg
  • Source
    DHTGA
Radiometer Pacific Pty Ltd
  • Empresa matriz del fabricante (2017)
    Danaher Corporation
  • Source
    DHTGA
Getinge Australia Pty Ltd
  • Empresa matriz del fabricante (2017)
    Getinge AB
  • Source
    DHTGA
Radiometer Pacific Pty Ltd
  • Empresa matriz del fabricante (2017)
    Danaher Corporation
  • Source
    DHTGA
Fresenius Medical Care Australia Pty Ltd
  • Empresa matriz del fabricante (2017)
    Fresenius SE & Co KGaA
  • Source
    DHTGA
Medtronic Australasia Pty Ltd
  • 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
    DHTGA
Philips Electronics Australia Ltd
  • Empresa matriz del fabricante (2017)
    Philips
  • Source
    DHTGA
Smith & Nephew Pty Ltd
  • Empresa matriz del fabricante (2017)
    Smith & Nephew plc
  • Source
    DHTGA
Elekta Pty Ltd
  • Empresa matriz del fabricante (2017)
    Elekta AB
  • Source
    DHTGA
Qiagen Pty Ltd
  • Empresa matriz del fabricante (2017)
    QIAGEN N.V.
  • Source
    DHTGA
Device Technologies Australia Pty Ltd
  • Empresa matriz del fabricante (2017)
    Device Technologies Australia Pty. Ltd.
  • Source
    DHTGA
Olympus Australia Pty Ltd
  • Empresa matriz del fabricante (2017)
    Olympus Corporation
  • Source
    DHTGA
Aidacare Pty Ltd
  • Empresa matriz del fabricante (2017)
    Snapmar Pty. Ltd.
  • Source
    DHTGA
Siemens Healthcare Pty Ltd
  • Empresa matriz del fabricante (2017)
    Siemens AG
  • Source
    DHTGA
William A Cook Australia Pty Ltd
  • Empresa matriz del fabricante (2017)
    Cook Group Incorporated
  • Source
    DHTGA
Becton Dickinson Pty Ltd
  • Empresa matriz del fabricante (2017)
    Becton, Dickinson and Company
  • Source
    DHTGA
Medtronic Australasia Pty Ltd
  • 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
    DHTGA
Medtronic Australasia Pty Ltd
  • 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
    DHTGA
Philips Electronics Australia Ltd
  • Empresa matriz del fabricante (2017)
    Philips
  • Source
    DHTGA
Getinge Australia Pty Ltd
  • Empresa matriz del fabricante (2017)
    Getinge AB
  • Source
    DHTGA
AMBU Australia Pty Ltd
  • Empresa matriz del fabricante (2017)
    Ambu Australia Pty Ltd
  • Source
    DHTGA
Regional Health Care Group Pty Ltd
  • Empresa matriz del fabricante (2017)
    Regional Health Care Group Pty Limited
  • Source
    DHTGA
Philips Electronics Australia Ltd
  • Empresa matriz del fabricante (2017)
    Philips
  • Source
    DHTGA
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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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