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Safety Information regarding COBAS® AmpliPrep/COBAS TaqMan® system using AMPILINK software v3.1x oder 3.2.x, Roche Diagnostics GmbH PDF, 384KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02179/10

Safety Notice concerning specific serial numbers of CT System Brilliance iCT (Heavyweight), Philips PDF, 1MB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group Radiological technology
Reference 02187/10

Recall of LEVO starting with serial number 913..., LEVO AG PDF, 286KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02255/10

Safety Notice for TREVO Retriever, Concentric Medical Inc. PDF, 520KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 00452/10

Lot recall of BI-20052 Endothelin ELISA, Biomedica Medizinprodukte GmbH PDF, 141KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02022/10

Safety Notice for External Pulse Generators PACE 203H, PACE 300 and Model 3085, Osypka Medical GmbH PDF, 246KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 02185/10

Follow-up information for corrective action for PK7300, Beckman Coulter (Olympus) PDF, 813KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 04891/08

Lot recall of Procedure Pak products, Mölnlycke Health Care AB PDF, 703KB, File does not meet accessibility standards Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group Dressings / Pads
Reference 02040/10

Recall for PTS Panels CHOL+HDL+GLU, Polymer Technology Systems PDF, 95KB, File is accessible Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 02474/10

Recall of GreenLight HPS™ 0010-2090 Laser Fibers, AMS PDF, 454KB, File is accessible Date: 25. August 2010 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering
Reference 00280/10