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Information about FC 500 with CXP Software, FC 500 MPL with MXP Software and CXP Analysis Software from Beckmann Coulter PDF, 191KB, File does not meet accessibility standards Date: 14. September 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02613/06

OptiMed recalls its "sinus-Carotid-RX-Systems". It was reported that the stent was difficult or not able to be released. PDF, 86KB, File does not meet accessibility standards Date: 08. September 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02549/06

Recall of the hip stems VerSys, Trabecular Metal, Mayo Conservative and ZMR from Zimmer PDF, 55KB, File does not meet accessibility standards Date: 08. September 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02249/06

Recall of TRIGEN KNEE NAIL from the company Smith & Nephew PDF, 33KB, File does not meet accessibility standards Date: 08. September 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 02454/06

Information for the pulse oximeter Oxipal OLV-2700K from Nihon Kohden PDF, 45KB, File does not meet accessibility standards Date: 08. September 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02300/06

Malfunction of the LIFEPAK® 20 defibrillators/monitors from Medtronic PDF, 91KB, File does not meet accessibility standards Date: 07. September 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02546/06

Recall of the "TUA" temporary pacing electrode with stylet from the company Dr Osypka PDF, 48KB, File does not meet accessibility standards Date: 07. September 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02350/06

Information for subsets of INSIGNIA and NEXUS pacemakers from Guidant PDF, 169KB, File does not meet accessibility standards Date: 06. September 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01794/06

Recall of Bacillol AF 500 ml and Bacillol plus 500 ml from Bode Chemie PDF, 47KB, File does not meet accessibility standards Date: 06. September 2006 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02414/06

Exchange of the spreader in patient hoists Arnold from Rebotec PDF, 155KB, File does not meet accessibility standards Date: 06. September 2006 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 02157/06