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Corrective action for the Pulsar-18 and Pulsar-35 peripheral self-expanding Nitinol stent systems, Biotronik AG PDF, 83KB, File does not meet accessibility standards Date: 02. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03047/15

Recall of the 4.5 mm Cortical Screws listed as compatible with the M/DN system, Zimmer Inc. PDF, 67KB, File does not meet accessibility standards Date: 02. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03200/15

Recall for the product Gelseal Straight, Vascutek Ltd. PDF, 139KB, File does not meet accessibility standards Date: 02. June 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 03198/15

Increased risk of cardiovascular death with use of ASV therapy (Weinmann devices SOMNOvent CR and prismaCR), Weinmann Geräte für Medizin GmbH + Co. KG PDF, 210KB, File does not meet accessibility standards Date: 02. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03027/15

Corrective action for the MAGNUS Hybrid OR table, MAQUET GmbH PDF, 796KB, File does not meet accessibility standards Date: 01. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 03215/15

Recall for the product TRACOE vario Tracheostomy Tube, TRACOE medical GmbH PDF, 295KB, File does not meet accessibility standards Date: 01. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 02982/15

Corrective action for the Spectron Multi Med Light valves, Spectron Gas Control Systems GmbH PDF, 100KB, File does not meet accessibility standards Date: 01. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 01979/15

Safety Notice concerning CombiSets® containing Medtronic Covidien Devon™ Light Glove, Paul Hartmann AG PDF, 41KB, File does not meet accessibility standards Date: 01. June 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 02871/15

Urgent Safety Notice for the IntraClude™ intra-aortic occlusion device Model ICF100, Edwards Lifesciences PDF, 48KB, File does not meet accessibility standards Date: 01. June 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 03138/15