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Correction of LIFEPAK® 12 und LIFEPAK® 20, Medtronic PDF, 34KB, File does not meet accessibility standards Date: 03. May 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 00900/06

Recall of DAKO Envision™+, Dako Cytomation PDF, 27KB, File does not meet accessibility standards Date: 03. May 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01202/06

Corrective action and recall for Glucose HK MOD P/D R2, Roche PDF, 58KB, File does not meet accessibility standards Date: 03. May 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00968/06

Correction of the temporomandibular joint program TM 4, SIRONA PDF, 15KB, File does not meet accessibility standards Date: 03. May 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 01087/06

Recall of Ball tip guide rods of the TriGen nail system, Smith & Nephew PDF, 52KB, File does not meet accessibility standards Date: 03. May 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00738/06

Software update for Precision 500D X-ray systems, GE Healthcare PDF, 56KB, File does not meet accessibility standards Date: 28. April 2006 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 00965/06

BioMerieux recalls the Slidex Rota-Kit 2 PDF, 94KB, File does not meet accessibility standards Date: 28. April 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01149/06

Delphi recalls the IVantage® Infusion System PDF, 35KB, File does not meet accessibility standards Date: 28. April 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01071/06

Corrective action for scooters Maxi 4 and Midi 4 plus, Days Healthcare PDF, 54KB, File does not meet accessibility standards Date: 28. April 2006 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01108/06

Recall of Acon Laboratories for the Quick-Chek Drug Screen PDF, 57KB, File does not meet accessibility standards Date: 27. April 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 00699/06