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Recall of the Femoral Venous Cannula Wire Reinforced from Sorin Group PDF, 70KB, File does not meet accessibility standards Date: 22. December 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03059/06

Advisory notice concerning the C3 blood line system from Gambro Dasco PDF, 168KB, File does not meet accessibility standards Date: 22. December 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02506/06

Safety risk of the birthing beds models Birthright 35000 and 170000 from Huntleight Healthcare PDF, 43KB, File does not meet accessibility standards Date: 22. December 2006 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02947/06

Recall of the ISP-Modularer-Duokopf from ISP PDF, 51KB, File does not meet accessibility standards Date: 22. December 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03677/06

Recall of the Tracheostoma Retainer Set manufactured by Willy Rüsch PDF, 79KB, File does not meet accessibility standards Date: 22. December 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03662/06

Software upgrade of the ORTHOPHOS Plus with TSA from the manufacturer Sirona Dental Systems PDF, 49KB, File does not meet accessibility standards Date: 22. December 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03742/06

Recall of the Powerlink with Visiflex infrarenal bifurcated delivery System from ENDOLOGIX PDF, 25KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03374/06

Recall of the central venous catheter Kids Cath NEO from Rüger Medical PDF, 28KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03434/06

Recall of the Level 1 Normothermic I. V. Fluid Administration Set from Smiths Medical PDF, 103KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03396/06

Stop of Delivery of the Metha Implant Components by Aesculap PDF, 33KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03387/06

Information concerning several products from Boston Scientific PDF, 76KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03669/06

Mandatory ugrade on all VISX™ WaveScan WaveFront™ Systems from Advanced Medical Optics PDF, 83KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 02624/06

Educational Brief regarding pain pump patient management with its programmable infusion systems from Medtronic PDF, 269KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01614/02

Recall of the superDimension Bronchus System and the superDimension Bronchus disposable system components from the company superDimension PDF, 35KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03611/06

Recall of the Fusion OMNI ERCP Catheter from Cook Endoscopy PDF, 33KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03379/06

Recall of Preface Sheaths from Biosense Webster PDF, 66KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03495/06

Information concerning the Codman Hakim valve programmers from Ethicon PDF, 93KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01777/06

Customer Information for several products of Thomashilfen GmbH PDF, 56KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 03027/06

Safety Information concerning the Proteus XR/a, Revolution XR/d and Definium 8000 X-ray systems from GE Healthcare PDF, 268KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01094/06

Recall of Frazier and Poole Suction Instruments from ConMed PDF, 88KB, File does not meet accessibility standards Date: 21. December 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03446/06

Corrective actions concerning the Dimension Articulated Stone Baskets from Bard PDF, 65KB, File does not meet accessibility standards Date: 20. December 2006 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03570/06

Information from Siemens concerning examinations which are opened under RIS control PDF, 63KB, File does not meet accessibility standards Date: 20. December 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03250/06

Information concerning the BrainSCAN version 5.2 or higher from BrainLAB PDF, 61KB, File does not meet accessibility standards Date: 20. December 2006 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03316/06

Recall of the BCI Autocorr Patientmonitors from Smiths Medical PDF, 105KB, File does not meet accessibility standards Date: 20. December 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03480/06

Recall of the Lumenis DuoTome SideLite™ 550 Micron Delivery System from Lumenis PDF, 107KB, File does not meet accessibility standards Date: 20. December 2006 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 03102/06

Corrective action for the Cell-Dyn 22 Calibrator and Cell-Dyn 22 Control from Abbott PDF, 138KB, File does not meet accessibility standards Date: 19. December 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03313/06

Information concerning the Picture Archiving and Communication System (PACS) syngo Imaging from Siemens PDF, 72KB, File does not meet accessibility standards Date: 19. December 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02701/06

Recall of the VAC Instill vacuum tubing from KCI Medical Products PDF, 53KB, File does not meet accessibility standards Date: 19. December 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03122/06