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Safety Information for the TDP® Gou Gong® lamp, T & K GmbH PDF, 44KB, File does not meet accessibility standards Date: 30. December 2010 Topics: Medical devices Type: Customer information

Product group Physical therapy
Reference 03954/10

Recall for the swivel shower chair model Ben, Drive Medical GmbH & Co. KG PDF, 90KB, File does not meet accessibility standards Date: 30. December 2010 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 04635/10

Safety Notice for Access® Immunoassay Systems SHBG, Beckman Coulter PDF, 49KB, File does not meet accessibility standards Date: 30. December 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02989/10

Safety Notice for all GE Healthcare MR systems, GE-Medical Systems PDF, 62KB, File does not meet accessibility standards Date: 30. December 2010 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 04658/10

Safety Notice for Brainlab iPlan RT Dose Radiotherapy Treatment Planning Software, Brainlab PDF, 73KB, File does not meet accessibility standards Date: 29. December 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04353/10

Safety Notice for all CyberKnife Treatment Planning Systems, Accuray PDF, 42KB, File does not meet accessibility standards Date: 29. December 2010 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 04534/10

Expansion of the Recall for Immunglobulin A (Ig-A) Reagent, Beckman Coulter PDF, 57KB, File does not meet accessibility standards Date: 29. December 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02468/10

Urgent Safety Notice for counterfeit Nellcor SpO2 Durasensors, PDF, 270KB, File does not meet accessibility standards Date: 29. December 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 04705/10

Recall for Zenith Branch Endovascular Graft Iliac Bifurcation, Cook PDF, 19KB, File does not meet accessibility standards Date: 29. December 2010 Topics: Medical devices Type: Customer information

Product group Non-active implants
Reference 04699/10

Recall for the Great Ormond Street GOS Tracheostomy Cannula Set, Teleflex Medical PDF, 189KB, File does not meet accessibility standards Date: 28. December 2010 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia
Reference 04706/10