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14,979 results

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ProSet Omnifix Syringe 5ml / 10ml, B. Braun Melsungen AG PDF, 42KB, File does not meet accessibility standards Date: 25. November 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 07582/14

Immediately in Effect Guidance Document: Product Labeling for Laparoscopic Power Morcellators PDF, 168KB, File does not meet accessibility standards Date: 25. November 2014 Topics: Medical devices Type: Download

Immediately in Effect Guidance Document: Product Labeling for Laparoscopic Power Morcellators

Field Safety Notice for AUTOGEN DR ICDs and CRT-Ds, Boston Scientific PDF, 419KB, File does not meet accessibility standards Date: 24. November 2014 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - defibrillators
Reference 07683/14

Recall Shuntassistent, Christoph Miethke GmbH & Co. KG PDF, 758KB, File does not meet accessibility standards Date: 24. November 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 07671/14

Field Safety Notice for PICO70 Arterial Blood Sampler, Radiometer Medical Aps. PDF, 20KB, File does not meet accessibility standards Date: 24. November 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 07640/14

PadPro & R2 Multifunction Electrodes, ConMed Corporation PDF, 80KB, File does not meet accessibility standards Date: 24. November 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 07614/14

Safety Advisory Notice for Mammography system Mammomat Inspiration/Fusion, Siemens AG PDF, 2MB, File does not meet accessibility standards Date: 24. November 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for mammographic diagnostics
Reference 07611/14

Recommendations on the approach to patients with Riata and Riata ST leads (St. Jude Medical) Date: 18. November 2014 Topics: Medical devices Type: Article

The German Cardiac Society (DGK) has published recommendations regarding patients with silicone insulated defibrillation leads Riata and Riata ST of St. Jude Medical.

Synthes GmbH: Lot Recall for Drill Bit 2.0 mm drilling depth 14 mm, 3-flute for Quick Coupling PDF, 736KB, File does not meet accessibility standards Date: 13. November 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07576/14

Safety Notice for the syngo Imaging XS, Siemens Healthcare PDF, 806KB, File does not meet accessibility standards Date: 13. November 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 07466/14

Additional and updated warnings and cautions for the HomeChoice Automated PD System and HomeChoice PRO Automated
PD System devices, Baxter
PDF, 68KB, File does not meet accessibility standards
Date: 13. November 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 07517/14

Recall for the Auxiliary Strap, SAM Medical Products PDF, 4MB, File does not meet accessibility standards Date: 13. November 2014 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - medico-mechanical devices
Reference 07524/14

Safety Notice for the Aeon Broaches – 38mm offset, Sheffield Medical Products Ltd. PDF, 100KB, File does not meet accessibility standards Date: 12. November 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07414/14

Safety Notice for the syngo.plaza, Siemens Healthcare PDF, 799KB, File does not meet accessibility standards Date: 12. November 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 05199/14

Urgent Safety Information for the TITAN operating table, TRUMPF Medizin Systeme GmbH + Co. KG PDF, 284KB, File does not meet accessibility standards Date: 12. November 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07295/14

Lot Recall for the Revaclear® / Revaclear Max® Dialyzers, Gambro Renal Products, Inc. PDF, 175KB, File does not meet accessibility standards Date: 12. November 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 07515/14

Recall for the Lotus™ Valve System, Boston Scientific International S.A. PDF, 170KB, File does not meet accessibility standards Date: 12. November 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - cardiac surgery
Reference 04897/14

Recall for the product CONTImove S version 2 - Power supply/charger, Buck Elektromedizin GmbH PDF, 3MB, File does not meet accessibility standards Date: 12. November 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 06293/14

Recall for the ProAQT-Sensor, PULSION Medical Systems SE PDF, 2MB, File does not meet accessibility standards Date: 12. November 2014 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electronic blood pressure monitor
Reference 07506/14

Safety Notice for Ysio Max, Luminos dRF Max and Luminos Agile Max with software version VE10 included SmartOrtho license, Siemens AG PDF, 3MB, File does not meet accessibility standards Date: 11. November 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 07300/14

Recall for IMMULITE®/IMMULITE® 1000 Turbo Troponin I assay, Siemens PDF, 27KB, File does not meet accessibility standards Date: 11. November 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 07297/14

Safety Notice for the CLINITEK Status, CLINITEK Status+, CLINITEK Status Connect System and CLINITEK Status Power Supply Adapter (Spare part), Siemens Healthcare Diagnostics PDF, 68KB, File does not meet accessibility standards Date: 11. November 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 07286/14

Urgent Safety Notice for the Zimmer® NexGen Trabecular Metal Tibial (Replacement) Impactor Pad Instruments, Zimmer, Inc. PDF, 131KB, File does not meet accessibility standards Date: 10. November 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 07447/14

Recall of Alcon INFINITI® Ultrasound Fluidik Management Systems (FMS) Single Use PAKs, Alcon Pharma GmbH PDF, 344KB, File does not meet accessibility standards Date: 10. November 2014 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 07464/14

Product Batch Recall for 3M™ ESPE™ RelyX™ Temp E NP (Cement, Dental, Zinc-Oxide Eugenol), 3M Deutschland GmbH PDF, 15KB, File does not meet accessibility standards Date: 10. November 2014 Topics: Medical devices Type: Customer information

Product group Dental products - dental material
Reference 07314/14

Important Safety Notice for the product MOSAIQ, Elekta PDF, 40KB, File does not meet accessibility standards Date: 10. November 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 07287/14

Merck Millipore: Urgent Safety Notice for Anti-Lea Murine IgA Blood Grouping Reagent, cell line GA2, Product Code NB PDF, 39KB, File does not meet accessibility standards Date: 10. November 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 06581/14

Recall for the port cannula Ambix NONCOR®stick Safe, Fresenius Kabi Deutschland AG PDF, 46KB, File does not meet accessibility standards Date: 07. November 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 06911/14

GE Healthcare nuclear medicine preventive maintenance procedure and schedule update notice for the Nuclear Medicine systems PDF, 181KB, File does not meet accessibility standards Date: 07. November 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 07319/14

Corrective action for the diode laser devices Medilas D12 (Medilas D Opal), Dornier MedTech GmbH PDF, 91KB, File does not meet accessibility standards Date: 07. November 2014 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - laser technology
Reference 07280/14