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Vista de la lista Vista de las tarjetas
  • Dispositivo 128
  • Fabricante 31827
  • Evento 155
  • Implante 27
Cook Incorporated
  • Empresa matriz del fabricante (2017)
    Cook Group Incorporated
  • Source
    TDMDAT
Cordis a Cardinal Health Company
  • Empresa matriz del fabricante (2017)
    Cardinal Health
  • Source
    TDMDAT
Cordis Cooperation
  • Empresa matriz del fabricante (2017)
    Cardinal Health
  • Source
    TDMDAT
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
    TDMDAT
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
    TDMDAT
Fresenius Medical Care AG & Co. KGaA
  • Empresa matriz del fabricante (2017)
    Fresenius SE & Co KGaA
  • Source
    TDMDAT
Greatbatch Medical
  • Empresa matriz del fabricante (2017)
    Integer Holdings Corporation
  • Source
    TDMDAT
Infopia. Co., Ltd.
  • Empresa matriz del fabricante (2017)
    Osang Healthcare Co. Ltd.
  • Source
    TDMDAT
International Biophysics Corp.
  • Empresa matriz del fabricante (2017)
    International Biophysics Corporation
  • Source
    TDMDAT
Intuitive Surgical Inc.
  • Empresa matriz del fabricante (2017)
    Intuitive Surgical Inc
  • Source
    TDMDAT
IRIS International
  • Empresa matriz del fabricante (2017)
    Danaher Corporation
  • Source
    TDMDAT
Johnson&Johnson International
  • Empresa matriz del fabricante (2017)
    Johnson & Johnson
  • Source
    TDMDAT
Leonhard Lang GmbH
  • Empresa matriz del fabricante (2017)
    Leonhard Lang Gmbh
  • Source
    TDMDAT
LivaNova Canada Corp.
  • Empresa matriz del fabricante (2017)
    LivaNova PLC
  • Source
    TDMDAT
MED-EL Elektromedizinische Geraete Gmbh
  • Empresa matriz del fabricante (2017)
    Med-El Elektromedizinische Geräte Gesellschaft M.B.H.
  • Source
    TDMDAT
Medivance
  • Empresa matriz del fabricante (2017)
    Becton, Dickinson and Company
  • Source
    TDMDAT
Medtronic 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
    TDMDAT
Verathon Medical
  • Empresa matriz del fabricante (2017)
    Roper Technologies Inc
  • Source
    TDMDAT
William Cook Europe ApS
  • Empresa matriz del fabricante (2017)
    Cook Group Incorporated
  • Source
    TDMDAT
Willy Rüsch GmbH
  • Empresa matriz del fabricante (2017)
    Teleflex Incorporated
  • Source
    TDMDAT
Medtronic 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
    TDMDAT
Micro Therapeutics, 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
    TDMDAT
Micro Vention Inc
  • Empresa matriz del fabricante (2017)
    Terumo Corp.
  • Source
    TDMDAT
NEWDEAL SAS
  • Empresa matriz del fabricante (2017)
    Integra LifeSciences Holdings Corporation
  • Source
    TDMDAT
Oridion Medikal 1987 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
    TDMDAT
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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.