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Safety Notice for Avance, Amingo and Aisys anaesthesia systems, GE Healthcare PDF, 125KB, File does not meet accessibility standards Date: 15. September 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03232/10

Safety Notice for Pentax Light Sources BS-LH 1; BS-LH 2; BS-LL 1, Pentax PDF, 127KB, File does not meet accessibility standards Date: 15. September 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03294/10

Safety Notice for Eclipse and RT Chart software, Varian Medical Systems PDF, 183KB, File does not meet accessibility standards Date: 15. September 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03216/10

Field Safety Notice for Certain GE Responder 2000 Defibrillators, Cardiac Science Corporation PDF, 124KB, File does not meet accessibility standards Date: 15. September 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02006/10

Follow-up Information for PLAC Test Reagent Kit Turbidimetric Immunoassay (TIA) Method, diaDexus PDF, 94KB, File does not meet accessibility standards Date: 14. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04090/09

Safety Notice for Fresenius Medical Care bloodlines, Fresenius Medical Care PDF, 72KB, File does not meet accessibility standards Date: 14. September 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02015/10

Safety Notice for Tonometer Measuring Prism, HAAG-STREIT AG PDF, 349KB, File does not meet accessibility standards Date: 14. September 2010 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02505/10

Customer Technical Bulletin concerning remote auto motions and differences on Clinac-software versions 6 and 7, Varian Medical Systems PDF, 624KB, File does not meet accessibility standards Date: 14. September 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01973/10

Safety Notice for Powerheart, Cardio Vive and Responder Defibrillators, Cardiac Science PDF, 65KB, File does not meet accessibility standards Date: 14. September 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04355/09

Recall for DePuy ASR™ Articular Surface Replacement and ASRXL Acetabular System, DePuy PDF, 134KB, File does not meet accessibility standards Date: 13. September 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01977/08

Safety Notice for HeartStart MRx monitor/defibrillators, Philips PDF, 188KB, File does not meet accessibility standards Date: 13. September 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01385/09

Urgent Recall for Solysafe Septal Occluder, Swissimplant PDF, 112KB, File does not meet accessibility standards Date: 13. September 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02800/10

Lot Recall for chronOS Cylinder and chronOS Insert, SYNTHES PDF, 49KB, File does not meet accessibility standards Date: 13. September 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03115/10

Safety Notice for Seraclone Anti-k (KEL2), Bio-Rad PDF, 83KB, File does not meet accessibility standards Date: 10. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01756/10

Safety Notice for Varian Treatment, Varian Medical Systems PDF, 126KB, File does not meet accessibility standards Date: 10. September 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03038/10

Information for UniCel Dxl 600 and 800 Systems Software Version 4.3 PDF, 269KB, File does not meet accessibility standards Date: 10. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02638/10

Safety Information for Intrathecal Catheters in drug delivery systems SynchroMed and IsoMed, Medtronic PDF, 22KB, File does not meet accessibility standards Date: 08. September 2010 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03166/10

Safety Notice for Connector HG 0286, Maquet PDF, 200KB, File does not meet accessibility standards Date: 08. September 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03153/10

Safety Notice for CS ceiling suspension, Philips PDF, 73KB, File does not meet accessibility standards Date: 08. September 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04704/09

Recall for Medi-Vac Non-Conductive Suction Tubings, Cardinal Health PDF, 46KB, File does not meet accessibility standards Date: 08. September 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03033/10

Safety Notice for IntelliVue Patient Monitors, Philips PDF, 115KB, File does not meet accessibility standards Date: 08. September 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03003/10

Lot Recall for suction catheters with funnel connectors, Unomedical PDF, 189KB, File does not meet accessibility standards Date: 07. September 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02556/10

Recall of a limited number of the automated external defibrillators (AEDs) HeartStart FRx 861304, HeartStart HS1 M5066A and HeartStart Home M5068A, Philips Healthcare PDF, 191KB, File does not meet accessibility standards Date: 07. September 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02003/10

Field Safety Notice concerning the Flexible Probe with Blocking Washer, GM11002420, Varian Medical Systems PDF, 118KB, File does not meet accessibility standards Date: 07. September 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01985/10

Safety Notice for INNOTEST ß-AMYLOID(1-42), Innogenetics PDF, 62KB, File does not meet accessibility standards Date: 07. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02082/10

Recall for ARCHITECT Sirolimus Reagent, list no. 01L76-25, lot no. 80162M100, Abbott PDF, 36KB, File does not meet accessibility standards Date: 07. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02024/10

Safety Notice for iVue100, Optovue PDF, 105KB, File does not meet accessibility standards Date: 06. September 2010 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02995/10

Safety Notice for Contasure Needleless, DIMA PDF, 14KB, File does not meet accessibility standards Date: 06. September 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02270/10

Recall for Impella® 5.0, ABIOMED PDF, 102KB, File is accessible Date: 06. September 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02414/10

Safety Notice for IGFBP-3 IRMA kits, Beckman Coulter PDF, 87KB, File is accessible Date: 03. September 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03085/10