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Recall of the CORDIS SV-5 and SV-8 Peripheral Steerable Guidewire PDF, 83KB, File does not meet accessibility standards Date: 10. August 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02165/06

Recall of special lots of the central venous catheter LogiCath AgTive and packs containing this catheter from Medex PDF, 82KB, File does not meet accessibility standards Date: 10. August 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02227/06

Corrective action for Clinical Chemistry from Abbott PDF, 72KB, File does not meet accessibility standards Date: 10. August 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02150/06

Recall of heat exchangers of the Gambro Integra Dialysis System by Gambro Dasco PDF, 100KB, File does not meet accessibility standards Date: 10. August 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01925/06

Recall of the products SafePico by Radiometer Medical PDF, 45KB, File does not meet accessibility standards Date: 10. August 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02021/06

Recall of the Defibrillator PIC 50 from the manufacturer WelchAllyn PDF, 139KB, File does not meet accessibility standards Date: 08. August 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01708/06

Recall of the Defibrillator AED 20 from the manufacturer WelchAllyn PDF, 77KB, File does not meet accessibility standards Date: 08. August 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01708/06

Recall of one lot-number Biolox V40 Delta Ceramic Head by Stryker Orthopedics PDF, 33KB, File does not meet accessibility standards Date: 04. August 2006 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 01501/06

Information about the Sonicath Ultra 6, 12.5 MHz Imaging Catheters from the company Boston Scientific International S.A. PDF, 63KB, File does not meet accessibility standards Date: 04. August 2006 Topics: Medical devices Type: Customer information

Product group Ultrasonics
Reference 01991/06

Corrective action and recall for Accu Chek Inform of the manufacturer Roche PDF, 125KB, File does not meet accessibility standards Date: 04. August 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01268/06

Information about the Multimed Light integrated valve for medical gases from the manufacturer Messer Cutting & Welding GmbH PDF, 105KB, File does not meet accessibility standards Date: 04. August 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01949/06

Corrective action and recall for the FP1000 Cell Preparation System of Beckman Coulter PDF, 56KB, File does not meet accessibility standards Date: 04. August 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01893/06

Corrective action for Ambu Silicone Plus Resusciators from the manufacturer Ambu PDF, 911KB, File does not meet accessibility standards Date: 04. August 2006 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 01909/06

Recall of the Cool-tip™ Ablation System from the company Tyco Healthcare Ltd. PDF, 55KB, File does not meet accessibility standards Date: 02. August 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01824/06

Recall of Model 7428 Kinetra from the manufacturer Medtronic PDF, 138KB, File does not meet accessibility standards Date: 02. August 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01922/06

Recall for the STA Cephascreen 4 reagent from the manufacturer Roche Date: 31. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02073/06

Recall of special lots of the 8F Bard® Channel Steerable Sheath from the manufacturer Enpath Medical Incorporation PDF, 178KB, File does not meet accessibility standards Date: 31. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 02100/06

Recall of intrathecal catheters model 8731 and distal revision kits for intrathecal catheter model 8598 form the manufacturer Medtronic PDF, 82KB, File does not meet accessibility standards Date: 31. July 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 02116/06