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15,004 results

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Additional Information concerning the corrective action for AMH Gen II Elisa, Beckman Coulter PDF, 88KB, File does not meet accessibility standards Date: 25. July 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 07449/12

Another Safety Notice concerning Series Unique Identifier (UID) issue associated with MR products, GE Healthcare PDF, 66KB, File does not meet accessibility standards Date: 24. July 2013 Topics: Medical devices Type: Customer information

Product group Electromedical fields
Reference 02864/13

Safety Notice concerning Series Unique Identifier (UID) issue associated with MR products, GE Healthcare PDF, 65KB, File does not meet accessibility standards Date: 24. July 2013 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 02864/13

Lot Recall for Lightspeed LSX Files, SYBRON PDF, 170KB, File does not meet accessibility standards Date: 23. July 2013 Topics: Medical devices Type: Customer information

Product group Dental products - instruments
Reference 01164/13

Safety Notice for Digital Accelerators with Electrons and Beam Modulator, MLCi/MLCi2, Agility or Asymmetric Heads, Elekta PDF, 129KB, File does not meet accessibility standards Date: 23. July 2013 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 03400/13, 03406/13

Lot Recall of the product CELT ACD (6F) Femoral Artery Vascular Closure Device, Vasorum Ltd. PDF, 404KB, File does not meet accessibility standards Date: 22. July 2013 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 03705/13

Lot Recall of the 27 G disposable cannula provided with the Amvisc® und Amvisc® Plus viscoelastic devices, Bausch & Lomb PDF, 2MB, File does not meet accessibility standards Date: 18. July 2013 Topics: Medical devices Type: Customer information

Product group ophthalmological technology - liquid media for ophthalmological purposes
Reference 07483/12

Lot Recall for BioMend®, BioMend Extend™, CollaCote®, CollaPlug® and CollaTape®, INTEGRA PDF, 54KB, File does not meet accessibility standards Date: 18. July 2013 Topics: Medical devices Type: Customer information

Product group Dental products - others
Reference 03167/13

Lot Recall of the product Interna® universal impression coping direct technique L 2mm und L 4mm, BTI PDF, 2MB, File does not meet accessibility standards Date: 15. July 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 02253/13

Safety Information for the manyfill filling injection kits, Medex PDF, 65KB, File does not meet accessibility standards Date: 15. July 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 07520/12