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Mode Liste Mode Grille
  • Dispositif médical 1003
  • Fabricant 257
  • Événement 124969
  • Implant 20
Avis De Sécurité sur blood lancets Tenderlett Adult Finger Incision Devices
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    00247/06
  • Date
    2006-02-16
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/06/2006/00247-06_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur ProTime Microcoagulation System from ITC
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    03757/06
  • Date
    2007-01-09
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/08/2006/03757-06_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur adult circle breathing systems
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    00843/05
  • Date
    2005-05-11
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/12/2005/00843-05_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur vascular prosthesis InterGard Knitted Heparin
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    00547/07
  • Date
    2007-03-02
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2007/00547-07_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur VI AUF Stent Graft and VI Extender Cuff
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    03073/06
  • Date
    2006-11-16
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2006/03073-06_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur ANA.NOVA® MII neck
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    02408/11
  • Date
    2011-06-06
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2011/02408-11_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur 8 mm EndoWrist Curved Scissor instrument
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    00661/05
  • Date
    2005-05-20
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/14/2005/00661-05_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur backrest tubes of the folding wheelchair Action³
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    01504/04
  • Date
    2005-08-09
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/15/2004/01504-04_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Dynymic Controls
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    01083/05
  • Date
    2005-08-26
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/15/2005/01083-05_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur height adjustable pushhandles on Action4
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    02271/05
  • Date
    2005-10-05
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/15/2005/02271-05_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur wheelchairs Typhoon and Tornado
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    02275/05
  • Date
    2005-09-30
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/15/2005/02275-05_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur wheelchairs Rea 705 Silencio-Care
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    00848/06
  • Date
    2006-04-27
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/15/2006/00848-06_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur an reinforcement of the backrests of the wheelchair model Spin-X
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    01791/07
  • Date
    2007-06-21
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/15/2007/01791-07_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Aptissen HealaFlow
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    600:41/01-261/16/01_33
  • Date
    2016-07-25
  • Pays de l'événement
    Singapore
  • Source de l'événement
    HSA
  • URL de la source de l'événement
    https://www.hsa.gov.sg/announcements
  • Notes / Alertes
    Data from Singapore is current through September 2018. All of the data comes from the Health Sciences Authority (HSA), 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 Singapore.
  • Notes supplémentaires dans les données
    Aptissen SA
Avis De Sécurité sur wheelchairs Invacare Action²
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    03315/07
  • Date
    2007-12-13
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/15/2007/03315-07_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Strep A Schnelltest-Streifen and the Strep A Schnelltest-Gerät from Innovacon
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    02577/07
  • Date
    2007-09-10
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/08/2007/02577-07_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur MRI-Patient Monitoring Systems Precess 3160
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    01622/07
  • Date
    2007-06-18
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/10/2007/01622-07_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur intraocular lenses GBR/ Vivarte Myopic and Newlife/Vivarte Presbyopic
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    00291/07
  • Date
    2007-04-03
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2007/00291-07_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur burs
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    02915/07
  • Date
    2007-09-06
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/06/2007/02915-07_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur ISP-Modularer-Duokopf
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    03677/06
  • Date
    2006-12-22
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/11/2006/03677-06_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur the HgbPro Professional Hemoglobin Testing System
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    02311/11
  • Date
    2011-06-03
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/08/2011/02311-11_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Arcadophta ® ARCOTANE C8F18 Purified Perfluoro-n-octane for Retinal Surgery
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    600:41/01-104/15/01_18
  • Date
    2015-12-14
  • Pays de l'événement
    Singapore
  • Source de l'événement
    HSA
  • URL de la source de l'événement
    https://www.hsa.gov.sg/announcements
  • Notes / Alertes
    Data from Singapore is current through September 2018. All of the data comes from the Health Sciences Authority (HSA), 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 Singapore.
  • Notes supplémentaires dans les données
    Arcadophta
Avis De Sécurité sur the device Power Adapter for Seiko Thermal Printer
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    04887/11
  • Date
    2011-11-11
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/08/2011/04887-11_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur ProTime3 Cuvettes
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    06348/12
  • Date
    2012-11-06
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/08/2012/06348-12_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
Avis De Sécurité sur Citrate Activated Partial Thromboplastin Time (APTT) Cuvettes
  • Type d'événement
    Field Safety Notice
  • ID de l'événement
    07905/13
  • Date
    2014-01-22
  • Pays de l'événement
    Germany
  • Source de l'événement
    BAM
  • URL de la source de l'événement
    https://www.bfarm.de/SharedDocs/Kundeninfos/EN/08/2014/07905-13_kundeninfo_en.html
  • Notes / Alertes
    German data is current through October 2018. All of the data comes from Bundesinstitut für Arzneimittel und Medizinprodukte, 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 Germany.
  • Notes supplémentaires dans les données
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À propos de cette base de données

Explorez plus de 120,000 rappels, alertes et avis de sécurité concernant les dispositifs médicaux, ainsi que leurs liens avec leurs fabricants.

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