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Safety Notice for Savanah Raised Toilet Seat Brackets, Homecraft Rolyan PDF, 137KB, File does not meet accessibility standards Date: 01. April 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 04094/08

Recall for the awl of the cosmicMIA spinal implantation system, Ulrich Medizintechnik PDF, 65KB, File does not meet accessibility standards Date: 01. April 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00576/09

Recall for Trigen Trochanteric Nail, Smith & Nephew PDF, 84KB, File does not meet accessibility standards Date: 31. March 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00822/09

Recall for VASOVIEW 6 Endoscopic Vessel Harvesting System kits, MAQUET PDF, 61KB, File does not meet accessibility standards Date: 31. March 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00580/09

Follow-up Field Safety Notice for S/5 iCentral and iCentral Client, GE Healthcare PDF, 99KB, File does not meet accessibility standards Date: 31. March 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01456/07

Recall for DARCO(R) Cannulated Hex Driver, Wright PDF, 63KB, File does not meet accessibility standards Date: 30. March 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00583/09

Safety Notice for GEMINI GXL and GEMINI TF Configurations, Philips PDF, 144KB, File does not meet accessibility standards Date: 30. March 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00712/09

Recall for Chocolate agar + PolyViteX VCAT 3, Biomerieux PDF, 83KB, File does not meet accessibility standards Date: 27. March 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00512/09

Safety Notice for iPlan RT Dose and VARIS version 6.2 or below, BrainLAB PDF, 105KB, File does not meet accessibility standards Date: 27. March 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 00526/09

Safety Information for ceramic Biolox cup, Aesculap PDF, 61KB, File does not meet accessibility standards Date: 27. March 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02873/08

Safety Notice for MultiDiagnost Eleva, UroDiagnost Eleva and OmniDiagnost Eleva Systems, Philips Healthcare PDF, 93KB, File does not meet accessibility standards Date: 27. March 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00713/09

Information for Brilliance CT Big Bore and CT Extended Brilliance Workspace, Philips Healthcare PDF, 211KB, File does not meet accessibility standards Date: 27. March 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00711/09

Safety Notice for ProMap Catheter, ProRhythm Inc. PDF, 132KB, File does not meet accessibility standards Date: 25. March 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04378/08

Safety Notice for Aisys and Avance Anaesthesia Machines, GE Healthcare PDF, 75KB, File does not meet accessibility standards Date: 25. March 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00559/09

Corrective Action for ABL80 FLEX CO-OX Analyzer, Radiometer PDF, 99KB, File does not meet accessibility standards Date: 25. March 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00577/09

Recall for Legion Press Fit stems, Smith & Nephew PDF, 55KB, File does not meet accessibility standards Date: 25. March 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00305/09

Recall for ITC60001 IMTEC ANA Screen and ITC70001 IMTEC ANA Screen (Cut-off), Human GmbH PDF, 8KB, File does not meet accessibility standards Date: 20. March 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00614/09

Safety Notice for VentrAssist LVAD Model LVA4 VA166 Blood Pump, Ventracor PDF, 77KB, File does not meet accessibility standards Date: 20. March 2009 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 00391/09

Information for Centricity RIS Software Version 4.Xi/Web Order-Option, GE Healthcare PDF, 81KB, File does not meet accessibility standards Date: 20. March 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00444/09

Recall for Model 515A Oxygen Concentrator, DeVilbiss PDF, 146KB, File does not meet accessibility standards Date: 19. March 2009 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 00322/09

Safety Notice for Exact Couch Top, Varian PDF, 2MB, File does not meet accessibility standards Date: 19. March 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 02940/08

Safety Notice for syringe pump A600 S with Software 0.93 until 4.3X, Codan Argus PDF, 106KB, File does not meet accessibility standards Date: 19. March 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00620/08

Recall for Internal Defibrillation Paddles and Handles without discharge control for use with LIFEPAK 9 or LIFEPAK 9P, Medtronic PDF, 71KB, File does not meet accessibility standards Date: 19. March 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00551/09

Safety Notice for iLED3, iLED5 and iLED5K Operating Theater Lighting Systems, Trumpf PDF, 185KB, File does not meet accessibility standards Date: 18. March 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 00491/09

Information for bath tube lift "Bellavita", Drive Medical PDF, 622KB, File does not meet accessibility standards Date: 18. March 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 03840/08

Safety Notice for BD Plastipak Luer Slip Syringes, Alcon PDF, 118KB, File does not meet accessibility standards Date: 18. March 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 04036/08

Safety Notice for Syngo Imaging PACS, Siemens PDF, 144KB, File does not meet accessibility standards Date: 18. March 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04818/08

Expanded Safety Notice for a subset of ICD-series CONTAK RENEWAL 4, VITALITY and VITALITY 2, BOSTON SCIENTIFIC PDF, 97KB, File does not meet accessibility standards Date: 18. March 2009 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01155/07

Safety Notice for Symbia® S- and T-Systems with Automatic Collimator Changer, Siemens PDF, 326KB, File does not meet accessibility standards Date: 18. March 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00228/09

Safety Notice for Babylux range, Maquet PDF, 397KB, File does not meet accessibility standards Date: 17. March 2009 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 03363/08