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14,984 results

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Safety Notice/Corrective action for Single Limb Circuit for Pneupac® Ventilators with PEEP Valve, Smiths Medical International Ltd. PDF, 332KB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 00131/15

Recall for the Alcon® Small Volume Syringes 200μL Luer-Lok™, Alcon Laboratories (UK) Ltd. PDF, 357KB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 00698/15

Recall for certain Hydrophilic Acrylic Single Use Intraocular Lens system packs, Rayner Intraocular Lenses Limited PDF, 4MB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00216/15

Follow-up Information for the Nanostim™ Leadless Pacemaker & Delivery System Catheter, St. Jude Medical PDF, 22KB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - cardiac pacemakers
Reference 04254/14

Recall for the product Cannulated screw 7.5, aap Implantate AG PDF, 312KB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00231/15

Updated Instructions for Use (IFU) for the Zenith Alpha™ Thoracic Endovascular Graft, Cook Medical PDF, 330KB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00326/15

Important Information for Baxter peritoneal dialysis Transfer sets, Titanium adapters, Disconnect caps and Clamshells PDF, 64KB, File does not meet accessibility standards Date: 24. February 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 00733/15

Urgent Safety Notice for the LANTIS™ Oncology Information System Server, Siemens AG PDF, 24KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 00279/15

Recall for the products REVISIO MTR Femur- und Tibiastiele, AQ Implants GmbH PDF, 2MB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 08716/14

Corrective action for the ISKD - Intramedullary Skeletal Kinetic Distractor (Limb Lengthener), Orthofix Inc. PDF, 167KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00139/15

Corrective action for the MRI systems with superconducting magnets, GE Healthcare PDF, 118KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 00448/15

Safety Notice for MiniCaps with Povidone-lodine, Baxter PDF, 255KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 00265/15

Urgent Safety Notice for the product Digital Linear Accelerator, Elekta Limited PDF, 268KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 00221/15

Urgent Safety Notice for the ACUSON S2000 Automated Breast Volume Scanner (ABVS), Siemens Medical Solutions USA, Inc. PDF, 6MB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 00089/15

Corrective action for the N Latex IgM, Healthcare Diagnostics PDF, 29KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 08453/14

Urgent Safety Notice for the Stiegelmeyer hospital beds, Joh. Stiegelmeyer GmbH & Co. KG PDF, 180KB, File does not meet accessibility standards Date: 23. February 2015 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - furnishings
Reference 04492/14

Urgent Safety Notice for the Philip’s Anesthesia Machines, DAMECA A/S / Philips Healthcare PDF, 49KB, File does not meet accessibility standards Date: 19. February 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 00055/15

Recall for the EasySpray Pressure Regulator, Tissomat and DuploSpray MIS Pressure, Baxter PDF, 416KB, File does not meet accessibility standards Date: 19. February 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 00204/15

Urgent Safety Notice for DigitalDiagnost systems Release 4.0.0 and 4.0.1, Philips Medical Systems PDF, 7MB, File does not meet accessibility standards Date: 19. February 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 00229/15

Recall for the ceramic Biolox delta Insert, Aesculap AG PDF, 484KB, File does not meet accessibility standards Date: 19. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00286/15