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Vista de la lista Vista de las tarjetas
  • Dispositivo 333
  • Fabricante 333
  • Evento 349
  • Implante 0
ARKRAY JAPAN
  • Empresa matriz del fabricante (2017)
    Arkray Inc.
  • Source
    NOM
Bausch & Lomb Incorporated
  • Empresa matriz del fabricante (2017)
    Bausch Health Cos., Inc.
  • Source
    NOM
Bausch & Lomb Incorporated
  • Empresa matriz del fabricante (2017)
    Bausch Health Cos., Inc.
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
BARD Limited UK
  • Empresa matriz del fabricante (2017)
    Becton, Dickinson and Company
  • Source
    NOM
Bard Peripheral Vascular Division, USA
  • Empresa matriz del fabricante (2017)
    Becton, Dickinson and Company
  • Source
    NOM
Becton Dickinson & Company Limited (Ireland)
  • Empresa matriz del fabricante (2017)
    Becton, Dickinson and Company
  • Source
    NOM
Becton, Dickinson & Company (UK)
  • Empresa matriz del fabricante (2017)
    Becton, Dickinson and Company
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
R&D Systems Inc.
  • Empresa matriz del fabricante (2017)
    Bio-Techne Corporation
  • Source
    NOM
Boston Scientific Corporation
  • Empresa matriz del fabricante (2017)
    Boston Scientific
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    NOM
Boston Scientific Corporation
  • Empresa matriz del fabricante (2017)
    Boston Scientific
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    NOM
Boston Scientific Corporation
  • Empresa matriz del fabricante (2017)
    Boston Scientific
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    NOM
Boston Scientific Limited (Ireland)
  • Empresa matriz del fabricante (2017)
    Boston Scientific
  • Comentario del fabricante
    “We take a patient-first approach to assessing the applicability of every recall and communicate to regulatory bodies in all geographies where the recalled device is sold,” Boston Scientific said in a statement to ICIJ. “We have coordinated several recalls across many countries in a timely manner,” the company said, adding that it complies with all national laws, which can often vary and require different processes for reporting information or taking action on recalls. The company said it uses a rigorous and uniform process to take action on recalls and that “when we initiate a field action (e.g. recall, safety alert), every customer who has received an affected product receives a communication that includes a letter for the physician.”
  • Source
    NOM
CHANGZHOU HEKANG MEDICAL INSTRUMENTS Co, Ltd,China
  • Empresa matriz del fabricante (2017)
    Changzhou Hekang Medical Instrument Co. Ltd.
  • Source
    NOM
Changzhou Hekang Medical Instruments Co., Ltd., China
  • Empresa matriz del fabricante (2017)
    Changzhou Hekang Medical Instrument Co. Ltd.
  • Source
    NOM
BIOMÉRIEUX INC, USA
  • Empresa matriz del fabricante (2017)
    Compagnie Merieux Alliance
  • Source
    NOM
bioMerieux SA
  • Empresa matriz del fabricante (2017)
    Compagnie Merieux Alliance
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
manufacturer #8496
  • Empresa matriz del fabricante (2017)
    Alamedics Gmbh & Co. Kg
  • Source
    NOM
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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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