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14,993 results

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Lot Recall for CLEAR-TRAC FLEXIBLE Reusable Obturators, Smith & Nephew Inc. PDF, 66KB, File does not meet accessibility standards Date: 24. January 2011 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 00088/11

Urgent Safety Notice for the LCS knee system with HP-instruments, DePuy PDF, 139KB, File does not meet accessibility standards Date: 24. January 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00028/11

Urgent Safety Notice for T.E.S.S.® Shoulder System, Biomet PDF, 143KB, File does not meet accessibility standards Date: 20. January 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04743/10

Recall for VITROS Chemistry Products PHYT Slides, Ortho-Clinical Diagnostics PDF, 68KB, File does not meet accessibility standards Date: 20. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04445/10

Information for syngo TrueD, Siemens PDF, 83KB, File does not meet accessibility standards Date: 20. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04615/10

Safety Notice for the CDI™ Blood Parameter Monitoring System, Terumo PDF, 102KB, File does not meet accessibility standards Date: 20. January 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04691/10

Recall for specific Intraaortic Balloon Counterpulsation Catheters, Arrow International PDF, 483KB, File does not meet accessibility standards Date: 20. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04817/10

Safety Notice/Recall for the Bard Lifestent Vascular Stent System, Angiomed PDF, 471KB, File does not meet accessibility standards Date: 19. January 2011 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 00019/11

Recall for MixMate 5353, Eppendorf AG PDF, 199KB, File does not meet accessibility standards Date: 19. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00027/11

Safety Notice for the HeadFIX® system, Elekta PDF, 606KB, File does not meet accessibility standards Date: 19. January 2011 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 03879/10