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15,022 results

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Recall regarding the 23 mm Engager™Transcatheter Aortic Bioprosthesis, Medtronic 3F Therapeutics, Inc. PDF, 112KB, File does not meet accessibility standards Date: 15. July 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - cardiac surgery
Reference 04162/15

Corrective action / Recall of several batches of SURESHOT Humeral 3.2 MM AO Drills, Smith & Nephew Inc. PDF, 74KB, File does not meet accessibility standards Date: 15. July 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04329/15

Safety Notice for the product BRAHMS PCT direct, BRAHMS GmbH, part of Thermofisher Scientific PDF, 3MB, File does not meet accessibility standards Date: 15. July 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 03501/15

Corrective action for the product iPlan RT Dose version 4.0 and 4.1, Brainlab AG PDF, 573KB, File does not meet accessibility standards Date: 15. July 2015 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 04179/15

Corrective action for the Precision 500D and Advantx Legacy/Legacy-D Radiographic and Fluoroscopic Systems, GE Healthcare PDF, 144KB, File does not meet accessibility standards Date: 15. July 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 04140/15

Safety Notice for the ACUSON S1000, ACUSON S2000, or ACUSON S3000 ultrasound systems, Siemens Medical Solutions USA, Inc./Ultrasound Business Unit PDF, 6MB, File does not meet accessibility standards Date: 15. July 2015 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 04143/15

Corrective Action Ceiling Supply Unit klinoPORT, TRUMPF Medizin Systeme GmbH + Co. KG PDF, 538KB, File does not meet accessibility standards Date: 15. July 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04121/15

Corrective action for the T-Lok™ Bone Marrow Biopsy products, Argon Medical Devices, Inc. PDF, 131KB, File does not meet accessibility standards Date: 15. July 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04010/15

Corrective action for the S3 Fluid Packs and S2 Fluid Packs (transponder defect), Roche Diagnostics PDF, 99KB, File does not meet accessibility standards Date: 14. July 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03295/15

Urgent Safety Notice for the product: MOSAIQ (Version 2.41 and higher), IMPAC Medical Systems, Inc. PDF, 37KB, File does not meet accessibility standards Date: 14. July 2015 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 04086/15