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14,972 results

Results per page: 10 20 30

Lot Recall of an infusion extension line named “T-connector Luer-Lock”, Hospira PDF, 550KB, File does not meet accessibility standards Date: 19. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 05721/12

Safety Notice for the Philips Essenta DR Compact, Philips Medical Systems PDF, 34KB, File does not meet accessibility standards Date: 19. September 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 05065/12

Recall for the Inflation Device, B. Braun Melsungen AG PDF, 29KB, File does not meet accessibility standards Date: 19. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03950/12

Urgent Safety Notice for Riata and Riata ST silicone insulated defibrillation leads, St. Jude Medical PDF, 609KB, File does not meet accessibility standards Date: 19. September 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - defibrillators
Reference 05563/11

Safety Notice for the Integrated Module Housing, Spacelabs Healthcare PDF, 35KB, File does not meet accessibility standards Date: 18. September 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 05803/12

Corrective action for Immulite 2000 / Immulite 2000 XPi Troponin I, Siemens PDF, 62KB, File does not meet accessibility standards Date: 18. September 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05896/12

Lot Recall for the Sarns™ Antegrade Cardioplegia Cannula, Terumo Europe NV PDF, 54KB, File does not meet accessibility standards Date: 18. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03905/12

Recall for Osseotite® Tapered Certain® Implants, BIOMET 3i PDF, 42KB, File does not meet accessibility standards Date: 18. September 2012 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 05638/12

Lot Recall for Sarns High-flow Aortic Arch Cannulas and Sarns Flexible Arterial Cannulas, Terumo Europe NV PDF, 67KB, File does not meet accessibility standards Date: 17. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03903/12

Recall for the SPIDER® Flexible Clip Applier, TransEnterix PDF, 47KB, File does not meet accessibility standards Date: 17. September 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 05169/12

Safety Notice for Mobile Monitoring Gateway (MMG) and Cardiomax, Ascom AB PDF, 102KB, File does not meet accessibility standards Date: 17. September 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 05061/12

Corrective action for the Previ Isola System, Biomerieux PDF, 58KB, File does not meet accessibility standards Date: 17. September 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 05849/12

Safety Notice for SureSigns VSi/VS2 Patient Monitors, Philips Healthcare PDF, 231KB, File does not meet accessibility standards Date: 17. September 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 05917/12

Safety Notice for the Bluephase G2 and Bluephase 20i Polymerisation Light, Ivoclar Vivadent AG PDF, 38KB, File does not meet accessibility standards Date: 14. September 2012 Topics: Medical devices Type: Customer information

Product group Dental products - equipment
Reference 04598/12

Safety Notice for LifeCare 4200 PCA Infusion System, Hospira Inc. PDF, 444KB, File does not meet accessibility standards Date: 14. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 05570/12

Safety Notice for the EkoSonic MACH4 Endovascular Device, EKOS Corporation PDF, 41KB, File does not meet accessibility standards Date: 14. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 05505/12

Safety Notice for Hemodraw® Closed Blood Sampling System, Smiths Medical PDF, 289KB, File does not meet accessibility standards Date: 14. September 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electronic blood pressure monitor
Reference 05041/12

Recall for the Terumo Syringe - 30ml Luer Lock/ Centric, Terumo Europe NV PDF, 334KB, File does not meet accessibility standards Date: 14. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 05835/12

Safety Notice for the superDimension systems with software version 4.0-4.9 PDF, 468KB, File does not meet accessibility standards Date: 14. September 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 04446/12

Safety Notice concerning the purification unit for medical air EcoPharm Tower, Dräger PDF, 289KB, File does not meet accessibility standards Date: 13. September 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05763/12