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Safety Notice for the Belmont®Rapid Infuser, Belmont PDF, 240KB, File does not meet accessibility standards Date: 02. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - equipment for collecting blood products and peripheral stem cells
Reference 03388/13

Safety Notice for the VenaFlow 30B-B and 30 BI-B, DJO Global PDF, 57KB, File does not meet accessibility standards Date: 02. July 2013 Type: Customer information

Product group Physical therapy - massage / mobility devices
Reference 03260/13

Safety Notice for the Liko® Overhead and Mobile Lifts - Standard SlingBar™ 450, Hill-Rom Company PDF, 833KB, File does not meet accessibility standards Date: 02. July 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 02783/13

Lot Recall of the Guide Wire Ø 2.5 mm with drill tip, lenghts 300 mm, DePuy Synthes PDF, 747KB, File does not meet accessibility standards Date: 02. July 2013 Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 02676/13

Safety Notice concerning the reusable CO2 absorbent canister, GE Healthcare PDF, 174KB, File does not meet accessibility standards Date: 02. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 03259/13

Recall for the BD Plastipak 50 ml Luer Lok Syringe, Becton Dickinson PDF, 48KB, File does not meet accessibility standards Date: 02. July 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 03531/13

Recall for the 1L Receptal Systems (Liners and Canisters), Hospira PDF, 447KB, File does not meet accessibility standards Date: 01. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 01916/13

Corrective action for Seraclone Anti-S, Biotest PDF, 601KB, File does not meet accessibility standards Date: 01. July 2013 Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 01899/13

Safety Notice concerning the Patient Transporter TRANSLIFE 4749.01A0, Maquet GmbH PDF, 206KB, File does not meet accessibility standards Date: 01. July 2013 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 02355/13

Safety Notice for the extension device 1150.59 AC, Maquet Getinge Group PDF, 179KB, File does not meet accessibility standards Date: 01. July 2013 Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 01002/13

Urgent Safety Notice for the DX-D 100 mobile X-ray system, AGFA Healthcare PDF, 96KB, File is accessible Date: 01. July 2013 Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 03022/13

Recall for Dimension Chemistry Wash, Siemens PDF, 52KB, File does not meet accessibility standards Date: 01. July 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02857/13

Corrective action for Phadia® 2500 EliA Instruments and Phadia® 5000 EliA Instruments, Phadia PDF, 33KB, File does not meet accessibility standards Date: 28. June 2013 Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 02953/13

Safety Information for the Accu-Check Combo Starter Kit, Roche Diagnostics GmbH PDF, 70KB, File does not meet accessibility standards Date: 28. June 2013 Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - infusion technology
Reference 02648/13

Safety Information for the T-Space PEEK Facelift Implants, AESCULAP PDF, 513KB, File does not meet accessibility standards Date: 28. June 2013 Type: Customer information

Product group Non-active implants - bone surgery
Reference 02787/13

Safety Notice concerning the RUSSKA walking frame vital 62, Ludwig Bertram GmbH PDF, 2MB, File does not meet accessibility standards Date: 28. June 2013 Type: Customer information

Product group Orthopaedic / Rehabilitation technology - daily living aids
Reference 02014/13

Recall for Lifecodes QuikScreen, Gen Probe PDF, 1MB, File does not meet accessibility standards Date: 28. June 2013 Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 02656/13

Safety Notice for the InSight Mini-C-arm Imaging System, Hologic PDF, 710KB, File does not meet accessibility standards Date: 28. June 2013 Type: Customer information

Product group Radiological technology - mobile radiological diagnostic facilities
Reference 02936/13

Safety Notice for the OFP-2 Flushing Pump, Olympus PDF, 51KB, File does not meet accessibility standards Date: 28. June 2013 Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 03303/13

Recall of several UltraClip® Dual Trigger Tissue Marker, Bard PDF, 123KB, File does not meet accessibility standards Date: 28. June 2013 Type: Customer information

Product group Medical instruments for use in humans - gynaecology
Reference 03376/13