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  • Dispositivo 2717
  • Fabricante 3081
  • Evento 3469
  • Implante 364
Notificaciones De Seguridad De Campo acerca de Ziploop Extended Toggleloc
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    444:2010/31845
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2011/Implantat-ortopedi--Ziploop-Extended-Toggleloc--Biomet-Sports-Medicine/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    AR10-47
  • Acción
    Revocation. The product is of incorrect length. The surgical technique can be modified and the operation time can be longer than expected.
Notificaciones De Seguridad De Campo acerca de Zimmer Universal Power System handsets
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2014-84765
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2014/Medicinsk-elektriskmekanisk-utrustning--Zimmer-Universal-Power-System-handenheter--Zimmer-Surgical-SA/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2014-74
  • Acción
    Information on the risk of use. Modification of products.
Notificaciones De Seguridad De Campo acerca de Ysio
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2014-71582
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2014/Diagnostiska-och-behandlande-stralningsprodukter--Ysio--Siemens-AG/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    UI XP048/14/S (mod.) & UI XP049/14/S (CSAN)
  • Acción
    Information on the risk of use. Modification of products.
Notificaciones De Seguridad De Campo acerca de Ysio-system
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2014-43189
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2014/Diagnostiska-och-behandlande-stralningsprodukter--Ysio-system--Siemens-AG/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    UI XP010/14/S
  • Acción
    Information on the risk of use. Modification of products.
Notificaciones De Seguridad De Campo acerca de Ysio Max, Max DRF Bright Bright Agile and Max
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2014-107538
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2015/Diagnostiska-och-behandlande-stralningsprodukter--Ysio-Max-Luminos-dRF-Max-och-Luminos-Agile-Max--Siemens-AG/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    XP080_14_S
  • Acción
    Warning information. Modification of the software. Temporary measures.
Notificaciones De Seguridad De Campo acerca de Ysio DRF and Luminos DRF
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2013-50494
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2013/Diagnostiska-och-behandlande-stralningsprodukter--Ysio-dRF-och-Luminos-dRF--Siemens-AG-Medical-Solutions/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    UI XP005/13/S
  • Acción
    Information on the risk of use. Modification of the software.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2015-87044
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2015/Medicinsk-programvara--VAS--Norrbottens-lans-landsting1/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2015-02
  • Acción
    Information on the risk of use. Modification of the software. Temporary measures.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2015-16709
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2015/Medicinsk-programvara--VAS--Norrbottens-lans-landsting/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2015-01
  • Acción
    Information on the risk of use. Modification of the software.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2017-38120
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN20161/Medicinsk-programvara--VAS--Region-Norrbotten/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2017-01
  • Acción
    Information on the risk of use. Modification of the software. Temporary measures.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2017-48007
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN20161/Medicinsk-programvara--VAS--Region-Norrbotten1/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2017-02
  • Acción
    Information on the risk of use. Modification of the software. Temporary measures.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2017-67891
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN20161/Medicinsk-programvara--VAS--Region-Norrbotten3/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2017-04
  • Acción
    Information on the risk of use. Modification of the software. Temporary measures.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2017-72518
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN20161/Medicinsk-programvara--VAS--Region-Norrbotten4/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2017-05
  • Acción
    Information on the risk of use. Modification of the software. Temporary measures.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2016-28934
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2016/Medicinsk-programvara--VAS--Norrbottens-lans-landsting1/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2016-02
  • Acción
    Information on the risk of use. Modification of the software. Temporary measures.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2016-39146
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2016/Medicinsk-programvara--VAS--Norrbottens-lans-landsting3/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2016-04
  • Acción
    Information on the risk of use. Modification of the software. Temporary measures.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2016-71164
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2016/Medicinsk-programvara--VAS--Norrbottens-lans-landsting5/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2016-06
  • Acción
    Information on the risk of use. Modification of the software. Temporary measures.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2016-91430
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN20161/Medicinsk-programvara--VAS--Norrbottens-lans-landsting/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2016-07
  • Acción
    Information on the risk of use. Modification of the software. Temporary measures.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2016-93593
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN20161/Medicinsk-programvara--VAS--Norrbottens-lans-landsting1/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2016-08
  • Acción
    Information on the risk of use. Modification of the software. Temporary measures.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2017-2395
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN20161/Medicinsk-programvara--VAS--Norrbottens-lans-landsting2/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2016-09
  • Acción
    Information on the risk of use. Modification of the software. Temporary measures.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2017-56385
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN20161/Medicinsk-programvara--VAS--Region-Norrbotten2/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2017-03
  • Acción
    Information on the risk of use. Modification of the software.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2017-92314
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN20161/Medicinsk-programvara--VAS--Region-Norrbotten5/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2017-06
  • Acción
    Information on the risk of use. Modification of the software.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2018-3075
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2018/Medicinsk-programvara--VAS--Region-Norrbotten/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2018-01
  • Acción
    Information on the risk of use. Modification of the software.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2018-5411
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2018/Medicinsk-programvara--VAS--Region-Norrbotten1/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2018-02
  • Acción
    Information on the risk of use. Modification of the software.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2018-23752
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2018/Medicinsk-programvara--VAS--Region-Norrbotten2/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2018-03
  • Acción
    Information on the risk of use. Modification of the software.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2016-15820
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2016/Medicinsk-programvara--VAS--Norrbottens-lans-landsting/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2016-01
  • Acción
    Information on the risk of use. Modification of the software.
Notificaciones De Seguridad De Campo acerca de VAS
  • Tipo de evento
    Field Safety Notice
  • ID del evento
    6.6.4-2016-39063
  • País del evento
    Sweden
  • Fuente del evento
    SMPA
  • URL de la fuente del evento
    https://lakemedelsverket.se/malgrupp/Halso---sjukvard/Medicinteknisk-sakerhetsinformation/fran-tillverkare/FSN2016/Medicinsk-programvara--VAS--Norrbottens-lans-landsting2/#
  • Notas / Alertas
    Swedish data is current through 2018. All of the data comes from the Swedish Medical Products Agency, except for the categories Manufacturer Parent Company and Product Classification.
    The Parent Company and the Product Classification were added by ICIJ.
    The parent company information is based on 2017 public records. The device classification information comes from FDA’s Product Classification by Review Panel, based on matches of data from the U.S. and Sweden.
  • Notas adicionales en la data
    2016-03
  • Acción
    Information on the risk of use. Modification of the software.
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Explore más de 120,000 registros de retiros, alertas y notificaciones de seguridad de dispositivos médicos y sus conexiones con los fabricantes.

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Historias en su correo

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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.