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Safety Notice for ARCHITECT i1000SR System, Abbott PDF, 30KB, File does not meet accessibility standards Date: 08. July 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02326/08

Safety Notice for Incubator 8000 Familie, Babytherm 8000 OC, RH 600, PP 800, PP 8000 and Babytherm 4200, Dräger Medical PDF, 182KB, File does not meet accessibility standards Date: 08. July 2008 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 02491/08

Safety Notice for Freedom Solo Heart Valves, Sorin Biomedica PDF, 174KB, File does not meet accessibility standards Date: 08. July 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02467/08

Information for m2000sp Instrument, Abbott PDF, 89KB, File does not meet accessibility standards Date: 08. July 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02503/08

Information for Allura Xper FD10 and FD10/10, Philips PDF, 102KB, File does not meet accessibility standards Date: 07. July 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02427/08

Recall RiwoMobile, Richard Wolf GmbH PDF, 124KB, File does not meet accessibility standards Date: 07. July 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01829/08

Information for Stress Table Echo 100 MED, ERGO-FIT PDF, 38KB, File does not meet accessibility standards Date: 04. July 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01721/08

Corrective action for Avantx-E, Innova 2000, 2100IQ, 3100/3100IQ, 4100/4100IQ and 2121IQ/3131IQ, GE Healthcare PDF, 186KB, File does not meet accessibility standards Date: 04. July 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02481/08

Recall tubing sets, Sorin PDF, 124KB, File does not meet accessibility standards Date: 04. July 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02363/08

Recall Covator Arthro Wand with Integrated Cable Wand, ArthroCare PDF, 94KB, File does not meet accessibility standards Date: 04. July 2008 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02231/08

Corrective action for COBAS INTEGRA 400/400 plus, Roche PDF, 123KB, File does not meet accessibility standards Date: 04. July 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02109/08

Corrective action for ADVIA 1200, 1650, 1800 and 2400, Siemens PDF, 104KB, File does not meet accessibility standards Date: 04. July 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02321/08

Information for Evita 2 dura, Evita 4 and Evita XL, Dräger PDF, 77KB, File does not meet accessibility standards Date: 03. July 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02397/08

Corrective action for COULTER GEN-S and LH SlideMakers, Beckman Coulter PDF, 43KB, File does not meet accessibility standards Date: 03. July 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02429/08

Information for Fabius Tiro, Dräger PDF, 65KB, File does not meet accessibility standards Date: 03. July 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02430/08

Information for dialysis tubing systems, Gambro Dasco PDF, 474KB, File does not meet accessibility standards Date: 02. July 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01763/08

Follow-up information for ARCHITECT c8000, Abbott PDF, 100KB, File does not meet accessibility standards Date: 02. July 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02009/08

Recall for Biolox forte, Corin PDF, 72KB, File does not meet accessibility standards Date: 01. July 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02388/08

Recall for Linton-Nachlas catheter, Coloplast A/S PDF, 84KB, File does not meet accessibility standards Date: 01. July 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02418/08

Safety notice for Revolution XR/d X-ray systems, GE Healthcare PDF, 44KB, File does not meet accessibility standards Date: 27. June 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02266/08

Information for Innova 2100IQ, 3100/3100IQ und 4100/4100IQ, GE Healthcare PDF, 90KB, File does not meet accessibility standards Date: 27. June 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02039/08

Security advice for SlimFlex-m 1.2.3, PhysIOL PDF, 1MB, File does not meet accessibility standards Date: 27. June 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02146/08

Recall Innex Knee Endoprosthesis, Zimmer PDF, 58KB, File does not meet accessibility standards Date: 27. June 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01209/08

Corrective action Architect Concentrated Wash buffer, Abbott PDF, 118KB, File does not meet accessibility standards Date: 27. June 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01306/07

Information for SENSE head coil 8 channel, Philips PDF, 167KB, File does not meet accessibility standards Date: 26. June 2008 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 00466/07

Information for CyberKnife® System, Accuray PDF, 66KB, File does not meet accessibility standards Date: 26. June 2008 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01960/08

Recall Livewire TC, St. Jude Medical PDF, 43KB, File does not meet accessibility standards Date: 26. June 2008 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02243/08

Information for Engström Carestation, GE Healthcare PDF, 153KB, File does not meet accessibility standards Date: 25. June 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 02100/08

Recall Thromboquik Reagent, Trinity Biotech PDF, 82KB, File does not meet accessibility standards Date: 25. June 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02194/08

Corrective action PT Link systems, Dako PDF, 101KB, File does not meet accessibility standards Date: 25. June 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01996/08