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  • Dispositivo 254
  • Fabricante 254
  • Evento 269
  • Implante 0
Notificaciones De Seguridad De Campo acerca de PSI kits, multi-lumen/PSI kits, CVC/PSI kits
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-04-15
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Central Venous Catheter (4004492)
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-05-15
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Axium neurostimulation system
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-05-15
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de HeartWare Ventricular Assist System
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-05-16
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de SeleXys DS Cup 48 uncemented
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-05-22
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de bondek and tevdek
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-05-23
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de PARACHUTE Guide Catheter
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-05-27
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de NexGen Complete Solution MIS Total Knee Procedure
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-06-10
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Charlie Guidewire HydroFinity
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-06-11
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Diabetes Implantable Insulin Pump MMT-2007D
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-06-17
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Empira and Empira NC
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-06-30
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de CloverSnare 4Loop Vascular Retrieval Snare
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-07-17
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Calcibon
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-07-17
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Stentless Biplex Biovalsalva / Thoraflex Hybrid / ...
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-07-17
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de RT-PLUS Modular Femoral Component
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-07-22
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Axium Implantable Lead Kit
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-07-23
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Celsite PICC-CEL
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-07-23
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Codman Certas Programmable Valve
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-07-24
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Perceval Sutureless Heart Valve
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-08-11
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Ellipse VR/DR
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-08-19
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Gender Solutions
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-08-19
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Portico Re-Sheathable Transcatheter Aortic Valve S...
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-09-12
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de triathlon femoral, scorpio femoral and restoration...
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-09-16
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de Echelon Endopath
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-09-17
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
Notificaciones De Seguridad De Campo acerca de EDS 3 CSF External Drainage System
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-09-18
  • País del evento
    Belgium
  • Fuente del evento
    AFMPS
  • URL de la fuente del evento
    https://www.afmps.be/fr/humain/produits_de_sante/dispositifs_medicaux/materiovigilance/fsn
  • Notas / Alertas
    Belgian data is current through November 2018. All of the data comes from the Federal Agency for Medicines and Health Products, 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 Belgium.
  • Notas adicionales en la data
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Acerca de la base de datos

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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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