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14,972 results

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Safety Notice for the Anaconda™ und Anaconda ONE-LOK™ Stent Grafts, Vascutek Ltd. PDF, 235KB, File does not meet accessibility standards Date: 05. March 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00975/12

Urgent Safety Notice for the RM Pressfit cup vitamys® und seleXys® Inlay vitamys®, Mathys PDF, 246KB, File does not meet accessibility standards Date: 05. March 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 01107/12

Safety Notice for syngo.plaza, Siemens Healthcare PDF, 500KB, File does not meet accessibility standards Date: 05. March 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 01067/12

Recall of Codman ICP Skull Bolt Kit, Codman PDF, 57KB, File does not meet accessibility standards Date: 05. March 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 00848/12

Safety Notice for Axiom Sensis XP, Siemens Healthcare PDF, 537KB, File does not meet accessibility standards Date: 02. March 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 00877/12

Safety Notice for DYONICS POWER II Control Unit, Smith &Nephew PDF, 40KB, File does not meet accessibility standards Date: 02. March 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 00538/12

Safety Notice for the OctoNova® Hemofiltration Device, Nikkiso PDF, 431KB, File does not meet accessibility standards Date: 02. March 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 04693/10

Recall of Intra Mobile Base, Planmeca PDF, 47KB, File does not meet accessibility standards Date: 02. March 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for stomatological diagnostics
Reference 06013/11

Recall of warming blanket of the Geratherm OP-Warming System, Geratherm Medical Diagnostic Systems PDF, 2MB, File does not meet accessibility standards Date: 01. March 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 01019/12

Recall for Fluitest CREA PAP, of Analyticon PDF, 106KB, File does not meet accessibility standards Date: 01. March 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00765/12

Recall for chronOS Putty, MATHYS PDF, 358KB, File does not meet accessibility standards Date: 01. March 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00844/12

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