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Corrective action for ADVIA 120 / 2120 Systems, Siemens PDF, 32KB, File does not meet accessibility standards Date: 27. May 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01737/08

Corrective action for Nephkit Alpha GST EIA Kit, Biotrin PDF, 84KB, File does not meet accessibility standards Date: 23. May 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01708/08

Recall TOPS and TOPS-on-Fusion System, MedNet PDF, 46KB, File does not meet accessibility standards Date: 23. May 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00307/08

Recall Vena Cava Filter, ALN implants chirurgicaux PDF, 98KB, File does not meet accessibility standards Date: 21. May 2008 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01239/08

Recall Proximate PPH Hemorrhoidal Circular Staplers, Ethicon PDF, 98KB, File does not meet accessibility standards Date: 21. May 2008 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01105/07

Recall Endopath ETS 35 mm, Johnson & Johnson PDF, 629KB, File does not meet accessibility standards Date: 21. May 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01704/08

Information for Multi RX, Multi SX, Fluoroscope 20 and Fluoroscope 90, Toshiba PDF, 45KB, File does not meet accessibility standards Date: 21. May 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00144/06

Information for X-Ray Systems with Monitor Ceiling Suspension, Philips PDF, 95KB, File does not meet accessibility standards Date: 21. May 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03903/07

Recall Archimedes, Codman PDF, 183KB, File does not meet accessibility standards Date: 20. May 2008 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01307/08

Information for Innova, GE Healthcare PDF, 155KB, File does not meet accessibility standards Date: 20. May 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00524/08

Information for Ambulift/Multilift, ArjoHuntleigh Ltd. PDF, 76KB, File does not meet accessibility standards Date: 16. May 2008 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment
Reference 00845/08

Information for HeartMate II, Thoratec Corp. PDF, 155KB, File does not meet accessibility standards Date: 16. May 2008 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01208/08

Information for Advantage Workstation, GE Healthcare PDF, 85KB, File does not meet accessibility standards Date: 16. May 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01690/08

Recall RP/VARD/20 and RP/VARD/35, MEDEX PDF, 164KB, File does not meet accessibility standards Date: 15. May 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01249/08

Corrective action for ADVIA Centaur CP AFP assay, Siemens PDF, 95KB, File does not meet accessibility standards Date: 15. May 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01600/08

Recall for Access und Access 2, Beckman Coulter PDF, 136KB, File does not meet accessibility standards Date: 15. May 2008 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01677/08

Safety Notice for MultiPlan®Treatment Planning Software Versions, Accuray PDF, 81KB, File does not meet accessibility standards Date: 14. May 2008 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01592/08

Safety Notice concerning LIV 2000, Linde PDF, 34KB, File does not meet accessibility standards Date: 14. May 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01673/08

Safety Notice concerning OEC devices, GE Healthcare PDF, 38KB, File does not meet accessibility standards Date: 14. May 2008 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01203/08

Recall Kryosonde, H.P. Braem AG PDF, 93KB, File does not meet accessibility standards Date: 14. May 2008 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01216/08