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14,979 results

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Corrective action of the HeartStart XL (M3735A) Defibrillator/Monitor battery M3561A, Philips Healthcare PDF, 67KB, File does not meet accessibility standards Date: 16. October 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 06142/12

Recall for L2 poly liner, SMR Shoulder System, Limacorporate PDF, 55KB, File does not meet accessibility standards Date: 16. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06173/12

Lot specific recall of the Trilogy® Acetabular System Shell with Cluster Holes, Zimmer Inc. PDF, 49KB, File does not meet accessibility standards Date: 15. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06272/12

Safety Notice for the Eclipse Treatment Planning System, Varian medical systems PDF, 335KB, File does not meet accessibility standards Date: 15. October 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 06038/12

Safety Notice for Phaco I/A Tubing Cassette Quicksets, Carl Zeiss Meditec AG PDF, 24KB, File does not meet accessibility standards Date: 15. October 2012 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - equipment for ophthalmological therapeutics
Reference 05090/12

Recall for the Cancellous Bone Impactor, Synthes GmbH PDF, 546KB, File does not meet accessibility standards Date: 15. October 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 06246/12

Urgent Safety Notice for Actifuse, BAXTER PDF, 49KB, File does not meet accessibility standards Date: 15. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - materials for implants
Reference 05767/12

Recall for Endoscopy suture anchors, SMITH & NEPHEW PDF, 55KB, File does not meet accessibility standards Date: 15. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05472/12

Corrective action for ADVIA Centaur systems Calibrator B and ADVIA Centaur FSH assay on the ADVIA Centaur and ADVIA Centaur XP system, Siemens PDF, 143KB, File does not meet accessibility standards Date: 12. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 05689/12

Safety Notice for the Brainlab Micro-Multileaf Collimator (MLC), Brainlab AG PDF, 675KB, File does not meet accessibility standards Date: 11. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - equipment for nuclear medical functional and localisation diagnostics
Reference 05736/12

Safety Notice concerning the Datex/GE compatible SpO2 sensor model S100A-300011, Solaris Medical PDF, 40KB, File does not meet accessibility standards Date: 11. October 2012 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices - electrodiagnostics
Reference 02991/12

Lot Recall for ILLICO cannulated polyaxial screws, ALPHATEC SPINE PDF, 94KB, File does not meet accessibility standards Date: 10. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06262/12

Recall of Proximal Tibial Spacers made of Tilastan, Waldemar Link GmbH & Co. KG PDF, 221KB, File does not meet accessibility standards Date: 10. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05284/12

Corrective action for the UniCel DxH 800 Coulter Cellular Analysis System, Beckman Coulter PDF, 100KB, File does not meet accessibility standards Date: 10. October 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 05743/12

Safety Notice concerning Brilliance CT Big Bore with software versions 2.4.7 and 2.4.8, Philips Healthcare PDF, 105KB, File does not meet accessibility standards Date: 10. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 06108/12

Safety Notice for the Femoral Segments - Endo-Model® SL® Rotational and Hinge Knee Prosthesis System, Waldemar Link GmbH & Co. KG PDF, 2MB, File does not meet accessibility standards Date: 09. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05277/12

Recall for MIRS Polyaxial Screw Body and MIRS Locking Cap, SYNTHES PDF, 444KB, File does not meet accessibility standards Date: 09. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05981/12

Safety Notice for the Centricity RIS-i system, GE Healthcare PDF, 33KB, File does not meet accessibility standards Date: 09. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 05873/12

Recall of further catalogue and batch numbers of the Cuticell Classic Paraffin Gauze, BSN medical GmbH PDF, 13KB, File does not meet accessibility standards Date: 09. October 2012 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - dressings
Reference 05354/12

Safety Notice for the Servoport 3000 m suction device, Servona GmbH PDF, 37KB, File does not meet accessibility standards Date: 09. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04549/12