BfArM - Federal Institute for Drugs and Medical Devices

Navigation and service

Search i

Search help

  • Enter one or more search terms in the search field. Upper and lower case are not relevant.
  • As soon as you have entered three letters in the search field, various search words will be suggested from which you can choose one.
  • If you are searching for a certain group of words, put these words in double quotes. The hits will then contain the words in the order you entered, e.g. "medicines for children".
  • Multiple search terms can also be combined with the Boolean operators AND and OR. When using the operator AND, the results contain the intersection of all search terms. When using the operator OR, the hits contain one of the search terms or only individual search terms. The result set is therefore significantly larger. Please note that these operators must be written in capital letters.
  • If you receive a (too) large number of hits as a result of your search, you can narrow it down by using filters. These filter options appear to the left of the search results and are subdivided into:

    • category (e.g. safety of medicinal products, medical devices, code systems)
    • format (e.g. download, risk information, DHPCs)
    • time interval (e.g. last 30 days, older than ...)
  • Selected filters can be removed individually or all at once ("Show all results").
  • By default, search results are sorted by relevance, but they can also be sorted chronologically ("Latest entries first" or "Oldest entries first").

Enter search term

15,394 results

Filter

Results per page: 10 20 30

Problem with the AB Portable Circulatory Support System, Abiomed Europe PDF, 34KB, File does not meet accessibility standards Date: 16. June 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01716/09

Field Safety Notice concerning 4.0 to 4.0.1 version on the Dental Application of the Extended Brilliance Workspace, Philips PDF, 86KB, File does not meet accessibility standards Date: 15. June 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01866/09

Recall of the scooter Strider Maxi 4 with serial numbers EV10FA-GM 01650 to EV10FA-GM 01907, Days Healthcare PDF, 69KB, File does not meet accessibility standards Date: 15. June 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01060/09

Field Safety Notice about an issue associated with the Corometrics 250 Maternal/ Fetal Monitors, GE Healthcare PDF, 64KB, File does not meet accessibility standards Date: 15. June 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01332/09

Exchange the castors of Pentax-Videocarts K125, K125E and K113, Knürr AG PDF, 121KB, File does not meet accessibility standards Date: 15. June 2009 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01645/06

Safety Notice for Avalon Fetal Monitors FM20 and FM30, Philips PDF, 116KB, File does not meet accessibility standards Date: 09. June 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01857/09

Information for AutoMate Sample Processing Systems, Beckman Coulter PDF, 104KB, File does not meet accessibility standards Date: 09. June 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01798/09

Information about the importance of regular AU Clinical Chemistry Analyser maintenance, Olympus Life Sciences Research Europe PDF, 74KB, File does not meet accessibility standards Date: 09. June 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01744/09

Recall for BD Insyte TM Autoguard TM IV Catheter, Becton Dickinson PDF, 120KB, File does not meet accessibility standards Date: 09. June 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01708/09

Recall for Valve Types OF-B136, OF-B140, OF-B163 and OF-B179, Pentax PDF, 123KB, File does not meet accessibility standards Date: 08. June 2009 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 01745/09

Safety Notice for ARTISTE MV, Siemens PDF, 138KB, File does not meet accessibility standards Date: 08. June 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01427/09

Safety Notice for NIOX® und NIOX® Flex, Aerocrine PDF, 55KB, File does not meet accessibility standards Date: 08. June 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01738/09

Safety Notice about the use of Wellion insulin reservoirs together with AccuChek FlexLink (Roche), Applied Diabetes Research PDF, 43KB, File does not meet accessibility standards Date: 08. June 2009 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00973/09

Recall of LactoSorb Pectus Stabilizer, Biomet PDF, 84KB, File does not meet accessibility standards Date: 05. June 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01513/09

Recall for Compass PIP Hinge, Smith & Nephew PDF, 50KB, File does not meet accessibility standards Date: 05. June 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00312/09

Recall for OIC Cage, Stryker PDF, 104KB, File does not meet accessibility standards Date: 04. June 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01262/09

Recall for DYONICS resection blades, Smith & Nephew PDF, 49KB, File does not meet accessibility standards Date: 04. June 2009 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 01722/09

Recall for Neuroform 3 Microdelivery Stent System, Boston Scientific PDF, 46KB, File does not meet accessibility standards Date: 04. June 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01769/09

Recall for PFC Sigma Femoral System, DePuy PDF, 161KB, File does not meet accessibility standards Date: 03. June 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01593/09

Safety Notice for Definium 5000, GE Healthcare PDF, 50KB, File does not meet accessibility standards Date: 03. June 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01698/09

Information for GALAXY system, LAP GmbH PDF, 43KB, File does not meet accessibility standards Date: 03. June 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01418/09

Safety Notice for Gemini TF 16 and 64, Gemini GXL 16 and Extended Brilliance Workspace, Philips PDF, 45KB, File does not meet accessibility standards Date: 03. June 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01642/09

Information for Incidin rapid, Ecolab PDF, 34KB, File does not meet accessibility standards Date: 03. June 2009 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 01444/09

Information for CellTracks® AutoPrep® System / Waste bottle, Veridex PDF, 115KB, File does not meet accessibility standards Date: 02. June 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01645/09

Recall for Mantis Rod Inserter Shaft, Stryker PDF, 211KB, File does not meet accessibility standards Date: 02. June 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01562/09

Safety Notice for 4DITC, Varian Medical Systems PDF, 403KB, File does not meet accessibility standards Date: 02. June 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01503/09

Safety Notice for CTL Array, Body Flex (M), and Body Flex (L) coil with GE Signa OpenSpeed MR Scanners, GE Healthcare PDF, 93KB, File does not meet accessibility standards Date: 02. June 2009 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 01413/09

Replacement of Wast Bottles for ABL700 and ABL800 Analysers, Radiometer PDF, 65KB, File does not meet accessibility standards Date: 02. June 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01630/09