• Acerca de la base de datos
  • ¿Cómo usar la IMDD?
  • Descargar la data
  • Preguntas frecuentes
  • Créditos
Vista de la lista Vista de las tarjetas
  • Dispositivo 121
  • Fabricante 121
  • Evento 122
  • Implante 0
Alerta De Seguridad para Hibiclen AV Foam
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 04 - 2018
  • Fecha
    2018-01-26
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2018/ALERTA_04-18.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Non conforming to the microbial limit test.
Alerta De Seguridad para EAR SYRINGE SMIC.
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 05 - 2015
  • Fecha
    2015-02-25
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2015/ALERTA_05-15.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Health record expired.
Alerta De Seguridad para LATEX EXAMINATION POWDERED GLOVES, Brand: Nipro
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 06 - 2014
  • Fecha
    2014-03-19
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2014/ALERTA_06-14.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Non conforming to the hole absence test.
Alerta De Seguridad para NON-STERILE LATEX EXAMINER GLOVES SIZE M
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 06 - 2016
  • Fecha
    2016-02-01
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2016/ALERTA_06-16.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Non conforming to the absence of holes test.
Alerta De Seguridad para NON-STERILE LATEX EXAM GLOVES SIZE L
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 06 - 2016
  • Fecha
    2016-02-01
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2016/ALERTA_06-16.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Non conforming to the hole detection test.
Alerta De Seguridad para unkown device
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 08 - 2017
  • Fecha
    2017-04-18
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2017/ALERTA_08-17.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Important information.
Alerta De Seguridad para STERILE SCALPEL BLADE (DISPOSABLE BISTURI LEAF)
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 10 - 2016
  • Fecha
    2016-03-07
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2016/ALERTA_10-16.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Non conforming to the corrosion resistance test.
Alerta De Seguridad para Latex examination gloves, non-sterile Qualatex brand
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 10 - 2017
  • Fecha
    2017-04-18
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2017/ALERTA_10-17.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Non conforming to the leak testing test.
Alerta De Seguridad para CATETER N ° 20 (CANULA IV without wings and without injection port)
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 11 - 2013
  • Fecha
    2013-05-06
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2013/ALERTA_11-13.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    It does not have an active sanitary registration.
Alerta De Seguridad para CENTRAL VENOUS CATHETER DOUBLE LUMEN
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 11 - 2013
  • Fecha
    2013-05-06
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2013/ALERTA_11-13.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    It does not have an active sanitary registration.
Alerta De Seguridad para INFUSION SET FOR SINGLE USE MICROGOTER - Infusim Sets for single use
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 11 - 2013
  • Fecha
    2013-05-06
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2013/ALERTA_11-13.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    It does not have a sanitary registration in force.
Alerta De Seguridad para DISPOSABLE SYRINGE x 10 mL with SANEX 21G x 1½ needle
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 11 - 2013
  • Fecha
    2013-05-06
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2013/ALERTA_11-13.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    It does not have an active sanitary registration.
Alerta De Seguridad para DISCHARGEABLE SYRINGE x 60 mL with 21G x 1½ needle
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 11 - 2013
  • Fecha
    2013-05-06
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2013/ALERTA_11-13.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    It does not have a sanitary registration in force.
Alerta De Seguridad para Clinical Kip Oral Thermometer
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 13 - 2017
  • Fecha
    2017-05-18
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2017/ALERTA_13-17.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Not compliant for the tests of: - thermometric liquid (liquid filling of the thermometer) - absence of defects.
Alerta De Seguridad para RENAX BLOOD LINE SET FOR HEMODIALYSIS MODEL SD G01 CODE S-01-G57-PB-14
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 16 - 2013
  • Fecha
    2013-08-15
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2013/ALERTA_16-13.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    They do not have sanitary registration.
Alerta De Seguridad para RENAX.AV FISTULA NEEDLE SET MODEL SD-A-16G-2CODE S-04-C15-B-03
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 16 - 2013
  • Fecha
    2013-08-15
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2013/ALERTA_16-13.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    They do not have sanitary registration.
Alerta De Seguridad para NATURAL LATEX EXAMINATION GLOVES "NON-DISPOSABLE STERILS" BRAND QUIMEDIC...
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 16 - 2016
  • Fecha
    2016-03-29
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2016/ALERTA_16-16.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Non conforming to the hole detection test.
Alerta De Seguridad para LATEX SEGUREX PRESERVATIVE
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 18 - 2015
  • Fecha
    2015-03-06
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2015/ALERTA_18-15.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Sanitary registry canceled due to final closure of the incumbent company.
Alerta De Seguridad para Wooden tongue depressor for adults
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 20 - 2004
  • Fecha
    2004-07-19
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2004/ALERTA_20-04.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Nonconforming sterility test.
Alerta De Seguridad para PROBE FOLEY 2 VIAS SIZE 18 FR / CH 30mL, box for 12 units
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 23 - 2014
  • Fecha
    2014-05-09
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2014/ALERTA_23-14.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Non conforming for the pyrogen test.
Alerta De Seguridad para Catgut chromic 1 (5 metric) 7cm round tip 30 mm 1/2 Circle
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 25 - 2004
  • Fecha
    2004-10-11
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2004/ALERTA_25-04.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Non conforming to the ph test.
Alerta De Seguridad para SYNGERS FOR ONE USE ONLY NIPRO BRAND (NIPRO SYNGERS FOR SINGLE USE) 20 m...
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 27 - 2015
  • Fecha
    2015-05-05
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2015/ALERTA_27-15.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Sanitary registry canceled.
Alerta De Seguridad para Pediatric urine collection bag, About x 1 unit (PEDIATRIC URINE COLLECTI...
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 29 - 2009
  • Fecha
    2009-07-16
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2009/ALERTA_29-09.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Non conforming to sterility and tightness tests.
Alerta De Seguridad para BLOOD BAGS CPD SAG-M.
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 29 - 2015
  • Fecha
    2015-05-27
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2015/ALERTA_29-15.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Health record expired.
Alerta De Seguridad para unkown device
  • Tipo de evento
    Safety alert
  • ID del evento
    ALERTA DIGEMID Nº 31 - 2016
  • Fecha
    2016-06-24
  • País del evento
    Peru
  • Fuente del evento
    Digemid
  • URL de la fuente del evento
    http://www.digemid.minsa.gob.pe/UpLoad/UpLoaded/PDF/Alertas/2016/ALERTA_31-16.pdf
  • Notas / Alertas
    Peruvian data is current through August 2018. All of the data comes from Digemid, 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 recall data from the U.S. and Peru.
  • Notas adicionales en la data
  • Causa
    Without sanitary registry.
  • « First
  • ‹ Prev
  • 1
  • 2
  • 3
  • 4
  • …
  • Next ›
  • Last »

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.

  • Preguntas frecuentes
  • Acerca de la base de datos
  • Contáctenos
  • Créditos

Historias en su correo

¿Trabaja en la industria médica? ¿O tiene experiencia con algún dispositivo médico? Nuestra reportería no ha terminado. Queremos oír de usted.

¡Cuéntanos tu historia!

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.

Descargar todo (zipped)