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14,979 results

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Weld control of the hoist Omnilift G2 Date: 27. August 2013 Topics: Medical devices Type: Article

Weld control of the hoist Omnilift G2 of the former manufacturer Weiner Innovative Medizintechnik

Corrective action for GlucoMen LX Sensor test strips, EurimPharm PDF, 100KB, File does not meet accessibility standards Date: 27. August 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 03844A/13

Lot recall of Scotchcast Wet or Dry Cast Padding, 3M Medica PDF, 28KB, File does not meet accessibility standards Date: 23. August 2013 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - dressings
Reference 04773/13

Information concerning change of expiration date, Johnson & Johnson PDF, 65KB, File does not meet accessibility standards Date: 21. August 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 04294/13

Lot recall of dialysis blood tubing system, B.Braun Avitum AG PDF, 48KB, File does not meet accessibility standards Date: 20. August 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - dialysis technology
Reference 02107/13

Batch Recall concerning Burr Hole Latex Free Probe Cover with Gel, Microtek Medical B.V. and Microtek Medical Malta Ltd. PDF, 3MB, File is accessible Date: 12. August 2013 Topics: Medical devices Type: Customer information

Product group Ultrasonics - ultrasonic diagnostic equipment
Reference 04069/13, 04071/13

Update of Safety Notice for GemStar Infusion System, Hospira Inc. PDF, 478KB, File does not meet accessibility standards Date: 12. August 2013 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 01284/13

Urgent Safety Notice for the SYNERGY® Circulatory Support System, CircuLite PDF, 132KB, File does not meet accessibility standards Date: 02. August 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 04341/13

Safety Information concerning ORBITER patient transfer system, Trumpf Medizin Systeme GmbH + Co. KG PDF, 43KB, File does not meet accessibility standards Date: 31. July 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 03588/13

Safety information for the ATP Software in devices for physical exercise (Genius Eco and Factum), Frei AG PDF, 132KB, File does not meet accessibility standards Date: 31. July 2013 Topics: Medical devices Type: Customer information

Product group Physical therapy - massage / mobility devices
Reference 05478/12

Recall of dental implants Osseotite Parallel Walled Certain, BIOMET 3i PDF, 52KB, File does not meet accessibility standards Date: 31. July 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 03645/13

Recall for Osseotite® 2 Certain® Prevail®, BIOMET 3i PDF, 327KB, File does not meet accessibility standards Date: 30. July 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 03643/13

Lot Recall of the product BEGO Semados® S4,1 L10, BEGO Implant Systems GmbH & Co. KG PDF, 193KB, File does not meet accessibility standards Date: 30. July 2013 Topics: Medical devices Type: Customer information

Product group Dental products - dental implants
Reference 03769/13

Safety Notice for the application of Test Stimulator, Model 3625, Medtronic Inc. PDF, 103KB, File does not meet accessibility standards Date: 30. July 2013 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 03900/13

Corrective action for ETI dsDNA, Dr. Fenning Biomed PDF, 369KB, File does not meet accessibility standards Date: 29. July 2013 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 04262/13, 04265/13

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