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Information about incorrect display of Pulsed Wave Doppler velosity values on reloaded images from GE Healthcare PDF, 111KB, File does not meet accessibility standards Date: 16. October 2007 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 03591/07

Recall of one lot of the Transend EX™ Standard .014-Guidewires from Boston Scientific PDF, 142KB, File does not meet accessibility standards Date: 16. October 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03576/07

Recommendations for patients concerning the Sprint Fidelis leads from Medtronic PDF, 379KB, File does not meet accessibility standards Date: 16. October 2007 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03656/07

Recall of the hydrophobic acrylic intraocular lens Hydromax from Carl Zeiss Meditec PDF, 120KB, File does not meet accessibility standards Date: 16. October 2007 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 03161/07

Information concerning the OBI versions 1.2 and 1.3 with CBCT from Varian PDF, 205KB, File does not meet accessibility standards Date: 16. October 2007 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03507/07

Recall of the Vasofix cannulae 1,1 x 33 mm, 20G from B. Braun PDF, 56KB, File does not meet accessibility standards Date: 15. October 2007 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 03441/07

Corrective Action of the programmer software for Reply SR single chamber pacemakers from Sorin PDF, 89KB, File does not meet accessibility standards Date: 12. October 2007 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 03232/07

Corrective action for the Swing Twin Sampler II from Diamed PDF, 35KB, File does not meet accessibility standards Date: 11. October 2007 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02817/07