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Safety Notice for the STERRAD® 200 System, ASP PDF, 46KB, File does not meet accessibility standards Date: 29. February 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00477/12

Corrective action for ABL80 FLEX Analyzers configured with either FLEX or BASIC software, Radiometer Medical PDF, 37KB, File does not meet accessibility standards Date: 29. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00377/12

Safety Notice for Varian Clinac® accelerators with Mark or Millennium MLC and BrainLAB m3 MLC, Varian medical systems PDF, 332KB, File does not meet accessibility standards Date: 29. February 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 00911/12

Safety Notice for the S4 Cervical Occiput screw remover and removal shaft, Aesculap PDF, 557KB, File does not meet accessibility standards Date: 29. February 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 00926/12

Safety Information for the surgical systems da Vinci S, da Vinci Si and da Vinci Si-e, Intuitive Surgical PDF, 236KB, File does not meet accessibility standards Date: 29. February 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 00845/12

Corrective Action for CYTO-STAT tetraCHROME, Beckman Coulter PDF, 176KB, File does not meet accessibility standards Date: 29. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00653/12

Korrekturmaßnahme für CYTO-STAT tetraCHROME, Beckman Coulter PDF, 36KB, File does not meet accessibility standards Date: 28. February 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 00653/12

Lot Recall for the Biosure-HA Interference Screw, SMITH&NEPHEW PDF, 70KB, File does not meet accessibility standards Date: 28. February 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00847/12

Safety Notice for a peritoneal dialysis set with a catheter adaptor manufactured by Covidien and distributed by Baxter, Baxter PDF, 106KB, File does not meet accessibility standards Date: 28. February 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 05330/11

Safety Notice concerning a corrective action of the electrophysiology (EP) system Carto 3, Biosense Webster PDF, 667KB, File does not meet accessibility standards Date: 27. February 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 00850/12