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  • Dispositivo 254
  • Fabricante 254
  • Evento 269
  • Implante 0
Notificaciones De Seguridad De Campo acerca de EasySept Hydro Plus Peroxide Solution
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2016-11-09
  • 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 Actifuse
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2015-08-24
  • 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 Synovis Life Technologies VASCU-GUARD Peripheral V...
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2016-07-05
  • 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 Floseal
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-10-10
  • 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 nMarq Irrigated Circular Catheter
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2015-06-22
  • 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 Pentaray catheters
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2016-04-22
  • 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 Pentaray catheters
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2017-05-03
  • 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 Thermocool Smarttouch catheters
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2014-10-24
  • 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 Orsiro coronary stent
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2015-06-22
  • 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 IntellaTip MiFi XP
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2015-11-30
  • 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 RotaWire Elite Guidewire and wireClip Torquer Guid...
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2015-10-16
  • 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 Watchman
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2015-08-27
  • 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 Imager II angiography catheter
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2016-12-19
  • 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 INGEVITY MRI endocardial pacing leads
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2016-11-30
  • 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 Lotus Valve System
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2016-08-05
  • 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 Advantage and Advantage Fit Transvaginal Sling Sys...
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2016-05-31
  • 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 Fetch 2 Aspiration Catheter
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2016-03-29
  • 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 AUTOGEN DAI DR and CRT-D defibrillators
  • Tipo de evento
    Field Safety Notice
  • 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 Cognis and DAI Teligen CRT-D
  • Tipo de evento
    Field Safety Notice
  • 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 Lotus Valve System
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2017-02-23
  • 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 SQ-RX Pulse Generator Model 1010 a component of th...
  • Tipo de evento
    Field Safety Notice
  • 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 Belzer UW cold storage solution
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2016-04-15
  • 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 Belzer cold storage solution
  • Tipo de evento
    Field Safety Notice
  • 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 Impella 2.5, Impella CP
  • Tipo de evento
    Field Safety Notice
  • Fecha
    2018-09-20
  • 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

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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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.

Descargar la data

La International Medical Devices Database está bajo la licencia Open Database License y sus contenidos bajo la licencia Creative Commons Attribution-ShareAlike . Al usar esta data, siempre citar al International Consortium of Investigative Journalists. Puede descargar acá una copia de la base de datos.

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