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14,972 results

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Urgent Safety Notice: Recall of Aquavent Heated Ventilator and CPAP Breathing Circuits, Armstrong Medical Ltd. PDF, 90KB, File does not meet accessibility standards Date: 05. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05986/12

Safety Notice for the Sorin S5/C5 Perfusion System, Sorin Group PDF, 559KB, File does not meet accessibility standards Date: 04. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05818/12

Safety Notice for the Carestream DRX-Evolution X-ray system, Carestream Health PDF, 24KB, File does not meet accessibility standards Date: 04. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 03918/12

Safety Notice for the Axio Lab.A1 microscope, Carl Zeiss Microscopy GmbH PDF, 85KB, File does not meet accessibility standards Date: 04. October 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - medical microscopes (does not incude laboratory microscopes)
Reference 06012/12

Lot Recall of BD Venflon Obturator 20GA, Becton Dickinson PDF, 43KB, File does not meet accessibility standards Date: 04. October 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - syringes and cannulas
Reference 06131/12

Safety Notice for Agfa HealthCare IMPAX® Cardiovascular (IMPAX CV) products, Agfa HealthCare PDF, 50KB, File does not meet accessibility standards Date: 04. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 05888/12

Safety Notice for Washer / disinfector (endoscope disinfection unit), Steris PDF, 61KB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - cleaning / disinfection / sterilisation
Reference 05076/12

Urgent Safety Notice for the BIRMINGHAM HIP Modular Head, Smith & Nephew PDF, 63KB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 06024/12

Safety Notice for Terumo® Advanced Perfusion System 1 / Network Power and communications, Terumo CVS PDF, 96KB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05654/12

Safety Notice for the air bubble detection system used with the Terumo® Advanced Perfusion System 1, Terumo CVS PDF, 91KB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05654/12

Safety Notice concerning the Sarns™ Centrifugal System for the Terumo® Advanced Perfusion System 1, Terumo CVS PDF, 79KB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 05654/12

Safety Notice concerning Brilliance CT 6, 16, MX8000 v. EXP and Gemini Dual systems, Philips PDF, 132KB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 06035/12

Safety Notice concerning MX 16-Slice CT systems, Philips PDF, 1MB, File does not meet accessibility standards Date: 02. October 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 06104/12

Recall for the Spiralok Suture Anchors, DEPUY MITEK PDF, 39KB, File does not meet accessibility standards Date: 01. October 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05869/12

Safety Notice for VISALIS S500 and VISALIS V500, Carl Zeiss Meditec AG PDF, 84KB, File does not meet accessibility standards Date: 01. October 2012 Topics: Medical devices Type: Customer information

Product group ophthalmological technology
Reference 04407/12

Urgent Product Recall for the PillCam® Express Delivery Devices, Given Imaging PDF, 41KB, File does not meet accessibility standards Date: 01. October 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 06064/12

Recall of the product Urgo Aphthen, Urgo GmbH PDF, 120KB, File does not meet accessibility standards Date: 01. October 2012 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - dressings
Reference 06095/12

Safety Notice concerning use of Oncentra MasterPlan and Oncentra External Beam, Nucletron PDF, 35KB, File does not meet accessibility standards Date: 01. October 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 05770/12

Recall for certain HLS Cannulae, MAQUET PDF, 470KB, File does not meet accessibility standards Date: 01. October 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 05972/12

FlowMedical PTA-CATH 5,0 x 100 Angioplasty Catheter of the manufacturer itm FlowMedical GmbH Date: 28. September 2012 Topics: Medical devices Type: Article

The recommendation that the Angioplasty Catheter FlowMedical PTA-CATH 5,0 x 100 of the manufacturer itm FlowMedical GmbH should not be used anymore is cancelled by BfArM