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14,982 results

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Corrective action for Immulite® and Immulite® 1000 Osteocalcin, Siemens PDF, 50KB, File does not meet accessibility standards Date: 26. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00708/14

Corrective action for ABX Pentra ML, Horiba ABX PDF, 1MB, File does not meet accessibility standards Date: 26. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00336/14

Corrective action for Alere Triage® TOX Drug Screen, Alere PDF, 165KB, File does not meet accessibility standards Date: 26. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00588/14

Lot Recall of the Cadisc®-L Lumbar Disc Replacement Device, RANIER Technology Ltd. PDF, 74KB, File does not meet accessibility standards Date: 25. February 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06890/13

Safety Notice for the Odalys Screwholder, Kisco International PDF, 181KB, File does not meet accessibility standards Date: 24. February 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00645/14

Lot Recall of the L-Varlock Cage/trial implantat holder, Kisco International PDF, 333KB, File does not meet accessibility standards Date: 24. February 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00569/14

Recall for the Midface Distractor, Synthes GmbH PDF, 66KB, File does not meet accessibility standards Date: 24. February 2014 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00074/14

Safety Notice for the Freka® Intestinal PEG-Tubes, Fresenius Kabi PDF, 73KB, File does not meet accessibility standards Date: 24. February 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - probes
Reference 06314/13

Recall for the Teleflex ISIS™ Tracheal Tubes with Subglottic Secretion Suction Port, Teleflex Medical PDF, 378KB, File does not meet accessibility standards Date: 21. February 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 00715/14

Safety Notice for the product Synchrony® Boom Arm Mounting Assembly, Accuray PDF, 3MB, File does not meet accessibility standards Date: 21. February 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 00303/14

Recall for the radial head prosthesis MoPyC, Tornier SAS PDF, 80KB, File does not meet accessibility standards Date: 21. February 2014 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00200/14

Important Safety Notice concerning Oxylog 2000 plus and Oxylog 3000 plus ventilators, Dräger Medical PDF, 2MB, File does not meet accessibility standards Date: 21. February 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 00793/14

Safety Notice for the product RaySearch RayStation 2.5, 3.0, 3.5 and 4.0, RaySearch Laboratories AB PDF, 412KB, File does not meet accessibility standards Date: 20. February 2014 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 00533/14

Urgent Safety Notice for the Flexible Bronchoscopes and Intubation Fiberscopes, Karl Storz GmbH & Co KG PDF, 202KB, File does not meet accessibility standards Date: 20. February 2014 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 07043/13

Corrective action for AXIOM ARTIS systems, Siemens Healthcare PDF, 2MB, File does not meet accessibility standards Date: 20. February 2014 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 00454/14

Corrective action for Thermo Scientific MAS® Omni Immune™ and MAS® Omni Immune™ Pro, Thermo Fisher PDF, 2MB, File does not meet accessibility standards Date: 20. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00287/14

Urgent Safety Notice for several Blood Glucose Monitoring Systems, Nipro Diagnostics PDF, 112KB, File does not meet accessibility standards Date: 19. February 2014 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05979/13

Safety Notice for the devices Cyto-Set Infusomat Space, Cyto-Set Mix and Cyto-Set Infusion line, B. Braun PDF, 124KB, File does not meet accessibility standards Date: 19. February 2014 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion kits
Reference 00189/14

Safety Notice for the Robotvario system, Miele & Cie. PDF, 1MB, File does not meet accessibility standards Date: 19. February 2014 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 05864/12

Safety Notice for Reusable Cranial Perforators, ACRA–CUT Inc. PDF, 1,007KB, File does not meet accessibility standards Date: 19. February 2014 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05879/12