BfArM - Federal Institute for Drugs and Medical Devices

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14,972 results

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Safety Notice for Savanah Raised Toilet Seat Brackets, Homecraft Rolyan PDF, 137KB, File does not meet accessibility standards Date: 01. April 2009 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 04094/08

Recall for the awl of the cosmicMIA spinal implantation system, Ulrich Medizintechnik PDF, 65KB, File does not meet accessibility standards Date: 01. April 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00576/09

Recall for Trigen Trochanteric Nail, Smith & Nephew PDF, 84KB, File does not meet accessibility standards Date: 31. March 2009 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00822/09

Recall for VASOVIEW 6 Endoscopic Vessel Harvesting System kits, MAQUET PDF, 61KB, File does not meet accessibility standards Date: 31. March 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00580/09

Follow-up Field Safety Notice for S/5 iCentral and iCentral Client, GE Healthcare PDF, 99KB, File does not meet accessibility standards Date: 31. March 2009 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01456/07

Safety risk concerning dental unit PROPHY RELAX Date: 30. March 2009 Topics: Medical devices Type: Article

The patient chair of the dental unit PROPHY RELAX could suddenly drop down from the selected position. BfArM recommends all users to check on the bearings in the spindle drive.

Recall for DARCO(R) Cannulated Hex Driver, Wright PDF, 63KB, File does not meet accessibility standards Date: 30. March 2009 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 00583/09

Safety Notice for GEMINI GXL and GEMINI TF Configurations, Philips PDF, 144KB, File does not meet accessibility standards Date: 30. March 2009 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00712/09

Recall for Chocolate agar + PolyViteX VCAT 3, Biomerieux PDF, 83KB, File does not meet accessibility standards Date: 27. March 2009 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00512/09

Safety Notice for iPlan RT Dose and VARIS version 6.2 or below, BrainLAB PDF, 105KB, File does not meet accessibility standards Date: 27. March 2009 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 00526/09