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14,970 results

Results per page: 10 20 30

Recall for Bicarbonate FS, DiaSys Diagnostic Systems PDF, 57KB, File does not meet accessibility standards Date: 11. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04804/10

Safety Notice: Swapped MR gradient cables, GE Healthcare PDF, 50KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 04649/10

Recall Information on certain Navigation software applications, Stryker PDF, 40KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04614/10

Lot Recall for Super Arrow-Flex® Percutaneous Sheath Introducer Set with Integral Hemostasis Valve / Side Port, Teleflex Medical PDF, 180KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04748/10

Lot Recall for Amplatzer Sizing Balloon II, AGA Medical Corp. PDF, 103KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04792/10

Safety Notice for MAGNETOM Systems, Siemens Healthcare PDF, 60KB, File does not meet accessibility standards Date: 10. January 2011 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 03891/10

Corrective Action/Recall for Sensors for Seronorm Trace Elements Serum Level 2, SERO PDF, 46KB, File does not meet accessibility standards Date: 07. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 03327/10

Lot Recall for FMS Intermediary Tube Sets for Fluid Management, DePuy Mitek PDF, 237KB, File does not meet accessibility standards Date: 07. January 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04675/10

Safety Notice for Spectra Optia Apheresis System, CaridianBCT PDF, 87KB, File does not meet accessibility standards Date: 07. January 2011 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 04637/10

Safety Notice for Licox CMP Tissue Oxygen Monitors, Integra LifeSciences PDF, 73KB, File does not meet accessibility standards Date: 07. January 2011 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04778/10

Important Information for Potassium liquirapid, HUMAN PDF, 77KB, File does not meet accessibility standards Date: 06. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04434/10

Safety Notice for the Footswitch of the Allura FD10, FD20, CV20 systems and the Allura field extension series, Philips PDF, 168KB, File does not meet accessibility standards Date: 06. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 04484/10

Safety Notice for GE Centricity PACS Web Diagnostic Software-Version 3.7.3, GE Healthcare PDF, 72KB, File does not meet accessibility standards Date: 06. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00228/10

Safety Notice for GE Centricity PACS Web Diagnostic Software, GE Healthcare PDF, 69KB, File does not meet accessibility standards Date: 06. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00228/10

Safety Notice for Presice Cryoablation Systems and SeedNet MRI Cryoablation Systems, GALILMedical PDF, 305KB, File does not meet accessibility standards Date: 05. January 2011 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04580/10

Safety Notice for Centricity™ PACS RA1000 Workstation Software Versions 2.1x und 3.0x, GE Healthcare PDF, 679KB, File does not meet accessibility standards Date: 05. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00360/10

Safety Notice for Centricity™ PACS RA1000 Workstation Software, GE Healthcare PDF, 569KB, File does not meet accessibility standards Date: 05. January 2011 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00360/10

Corrective Action/Recall for SYNCHRON Systems Glucose (GLU) Cartridge Reagent for use on UniCel and SYNCHRON Systems, Beckman Coulter PDF, 138KB, File does not meet accessibility standards Date: 05. January 2011 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04462/10

Safety Notice for Riata and Riata ST silicone insulated defibrillation leads, St. Jude Medical PDF, 190KB, File does not meet accessibility standards Date: 04. January 2011 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 04703/10