BfArM - Federal Institute for Drugs and Medical Devices

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14,993 results

Results per page: 10 20 30

Safety Notice for DePuy S-ROM Noiles Distal Femoral Cutting Guide, DePuy Orthopaedics Inc. PDF, 80KB, File does not meet accessibility standards Date: 09. November 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03952/10

Corrective Action for HemoCue Glucose 201 DM and HemoCue Hb 201 DM Analyzers, HemoCue AB PDF, 174KB, File does not meet accessibility standards Date: 09. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03733/10

Extended Recall of 1 Day Acuvue TruEye™ contact lenses, Johnson & Johnson Vision Care PDF, 178KB, File does not meet accessibility standards Date: 09. November 2010 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 03962/10

Corrective Action for CYTO-STAT tetraCHROME reagents, Beckman Coulter PDF, 54KB, File does not meet accessibility standards Date: 09. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03922/10

Safety Notice for Sureshot Targeter, Smith & Nephew PDF, 830KB, File does not meet accessibility standards Date: 08. November 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03766/10

Important Safety Notice for ADT inbound interface to MOSAIQ or Multi-ACCESS, Elekta IMPAC SOFTWARE PDF, 26KB, File does not meet accessibility standards Date: 08. November 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03376/10

Recall for Mediselect II and Medireg II, GCE, s.r.o. Date: 08. November 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01811/10

Recall and extended recall of the Lavanid 1 and Lavanid 2 wound irrigation solution, Serag-Wiessner KG PDF, 185KB, File does not meet accessibility standards Date: 08. November 2010 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 03783/10

Safety Notice for Essenta DR Compact, Philips PDF, 105KB, File does not meet accessibility standards Date: 08. November 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03441/10

Recall for Universal IVF Medium, Origio PDF, 38KB, File does not meet accessibility standards Date: 05. November 2010 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 03791/10

Safety Notice for the Young LoTrach ™ Tracheostomy Tubes, Venner Medical (Singapore) PDF, 122KB, File does not meet accessibility standards Date: 05. November 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03802/10

Safety Notice for ULTRA SteriSet, Gambro Industries PDF, 211KB, File does not meet accessibility standards Date: 05. November 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03983/10

Recall for ATEC® Breast Biopsy and Excision System-ATEC Handpiece, Hologic, Inc. PDF, 250KB, File does not meet accessibility standards Date: 05. November 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03077/10

Information on submission of a request for authorisation of a clinical trial or a performance study / evaluation PDF, 29KB, File is accessible Date: 04. November 2010 Topics: Medical devices Type: Download

Information on submission of a request for authorisation of a clinical trial or a performance evaluation to the Federal Institute for Drugs and Medical Devices (Bundesinstitut für Arzneimittel und Medizinprodukte, BfArM) in accordance with …

Safety Information for hospital bed model Avanta, Joh. Stiegelmeyer GmbH & Co. KG PDF, 736KB, File does not meet accessibility standards Date: 04. November 2010 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 03387/10

Urgent Safety Notice for Dual-Chamber External Temporary Pulse Generator Model 5388, Medtronic PDF, 39KB, File does not meet accessibility standards Date: 04. November 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03748/10

Recall for PleuraSeal Lung Sealant System, COVIDIEN PDF, 97KB, File does not meet accessibility standards Date: 04. November 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03779/10

Field Safety Notice concerning a problem with OMRIX Pressure Regulator to administer Fibrin Sealants, Ethicon, Inc., a Johnson & Johnson company PDF, 80KB, File does not meet accessibility standards Date: 04. November 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03379/10

Safety Notice for Maquet Heart Lung Machine HL20, Maquet PDF, 81KB, File does not meet accessibility standards Date: 03. November 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03745/10

Recall for Carto® 3 System Interface Cable, Biosense Webster PDF, 118KB, File does not meet accessibility standards Date: 03. November 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03749/10

Safety Notice for ALPHAMAQUET operationg table columns PDF, 75KB, File does not meet accessibility standards Date: 03. November 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 03800/10

Safety Notice for Signa OpenSpeed and Signa Ovation, GE Healthcare PDF, 63KB, File does not meet accessibility standards Date: 02. November 2010 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 03788/10

Safety Notice concerning the radiotherapy planning software XiO, Elekta CMS Software PDF, 77KB, File does not meet accessibility standards Date: 02. November 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03315/10

Lot Recall of the Original-Infusomat line, B. Braun PDF, 63KB, File does not meet accessibility standards Date: 02. November 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03741/10

Lot Recall of the EnduRo meniscal component, Aesculap PDF, 102KB, File does not meet accessibility standards Date: 02. November 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03703/10

Lot Recall for Sopira Carpule Needles, HERAEUS PDF, 99KB, File does not meet accessibility standards Date: 29. October 2010 Topics: Medical devices Type: Customer information

Product group Dental products
Reference 03255/10

Recall for BD CD10 products, Becton Dickinson PDF, 106KB, File does not meet accessibility standards Date: 29. October 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03370/10