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Safety Notice concerning a corrective action of the HeartStart MRx Monitor/Defibrillator, Philips Healthcare PDF, 61KB, File does not meet accessibility standards Date: 06. June 2013 Type: Customer information

Product group Medical electronics / Electromedical devices - electrotherapy
Reference 02913/13

Safety Notice for COHERENCE Therapist 2.3, Siemens Healthcare PDF, 39KB, File does not meet accessibility standards Date: 05. June 2013 Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 01350/13

Lot Recall for the product Confidence Spinal Cement System Kit, DEPUY PDF, 51KB, File does not meet accessibility standards Date: 05. June 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 02334/13

Recall of Omrix Pressure Regulators, Ethicon Biosurgery PDF, 24KB, File does not meet accessibility standards Date: 05. June 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02634/13

Intuitive Surgical, Inc.: Safety Notice for surgical systems da Vinci S, Si and Si-e PDF, 40KB, File does not meet accessibility standards Date: 05. June 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 02180/13

Recall of specified Intuitive Surgical Bipolar Instruments used with the da Vinci Standard System (IS1200), Intuitive Surgical, Inc. PDF, 146KB, File does not meet accessibility standards Date: 05. June 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02964/13

Recall for the LCP Distal Femoral Plate, SYNTHES PDF, 68KB, File does not meet accessibility standards Date: 04. June 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 02339/13

Corrective Action for the Output plate of the MagNA Pure 96 instrument, Roche PDF, 39KB, File does not meet accessibility standards Date: 04. June 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 01685/13

Recall of the iMRI Registration Matrix for GE Headholder of the Cranial Navigation System, Brainlab AG PDF, 139KB, File does not meet accessibility standards Date: 04. June 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02898/13