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14,989 results

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Recall of several catalog numbers of Scorpio NRG 4:1 cutting blocks, Stryker Orthopaedics PDF, 31KB, File does not meet accessibility standards Date: 15. November 2010 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 03400/10

Follow-up/Updates for CellTracks AutoPrep System, Ortho-Clinical Diagnostics / Veridex PDF, 155KB, File does not meet accessibility standards Date: 12. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01979/10

Safety Notice for Ultraview SL 2200, 2400 and 2600 Monitore with Wireless-Option, Spacelabs Medical PDF, 78KB, File does not meet accessibility standards Date: 12. November 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 03550/10

Lot Recall for BD 5 ml Plastipak Syringe Luer-Lok-Tip, Becton Dickinson PDF, 24KB, File does not meet accessibility standards Date: 11. November 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04152/10

Corrective Action for Core TDM Multi-Calibrator, Part no.. ODC6411 (Lot no. 0021 and 0022), Beckman Coulter PDF, 91KB, File does not meet accessibility standards Date: 11. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03461/10

Corrective Action for G-6-PDH Control, Trinity Biotech PDF, 391KB, File does not meet accessibility standards Date: 11. November 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03963/10

Important Notice for XVI, Elekta Ltd. PDF, 240KB, File does not meet accessibility standards Date: 11. November 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03226/10

Safety Notice for Sarns Ultrasonic Air Sensor-Cable, Terumo PDF, 144KB, File does not meet accessibility standards Date: 11. November 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04001/10

Safety Notice for OEC 9800 and 9900 X-ray systems (C-Arm), GE Healthcare PDF, 52KB, File does not meet accessibility standards Date: 11. November 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 03750/10