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14,984 results

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Important Safety Notice for the AC 2000 spring arms, Ondal Medical Systems GmbH PDF, 325KB, File does not meet accessibility standards Date: 02. March 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 07767/14

Recall for Titan™ Stabilizer and Titan™ 360 Stabilizer, Terumo Cardiovascular Systems (Terumo CVS) PDF, 92KB, File does not meet accessibility standards Date: 02. March 2015 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - cardiac/thorax surgery
Reference 00735/15

Safety Notice for the Bead Block (Embolic Bead) device, Biocompatibles UK Ltd. PDF, 1MB, File does not meet accessibility standards Date: 02. March 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 00585/15

Safety Notice for the Access 2 Systems, Beckman Coulter PDF, 19KB, File does not meet accessibility standards Date: 02. March 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00709/15

Safety Notice for the Wound-EL Dressing Electrode 15x15cm (10x10cm), Mölnlycke Health Care PDF, 22KB, File does not meet accessibility standards Date: 02. March 2015 Topics: Medical devices Type: Customer information

Product group Dressings / Pads - dressings
Reference 00117/15

Safety Notice for the Product Compass 3.1 and 3.1a, IBA Dosimetry GmbH PDF, 4MB, File does not meet accessibility standards Date: 02. March 2015 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiation facilites with accelerators for teletherapy
Reference 00696/15

Corrective action for the Sealing Screw Tibia UC, Peter Brehm GmbH PDF, 453KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00940/15

Recall for the GENESIS II non-porous Tibial Baseplate, Smith & Nephew PDF, 77KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 00870/15

Urgent Safety Notice for the Edwards Commander Delivery System, Edwards Lifesciences LLC PDF, 82KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - catheters
Reference 00669/15

Corrective action for ADVIA Centaur Systems Progesterone Kits, Siemens Healthcare Diagnostics Inc. PDF, 26KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00462/15

Corrective action for the ADVIA Chemistry Systems Drug Calibrator I, Siemens Healthcare Diagnostics Inc. PDF, 27KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 00278/15

Safety Notice for the SD BIOLINE Malaria Ag products containing single-use buffer ampoule, Standard Diagnostics, Inc. PDF, 2MB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 00619/15

Recall for the Stryker System 6 Aseptic Housings, Stryker Instruments PDF, 255KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 00135/15

Corrective action for Siemens Capillary Caps, Siemens Healthcare Diagnostics Inc. PDF, 24KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - instruments, apparatuses and systems
Reference 00527/15

Urgent Safety Notice for the DuraDiagnost X-Ray system, Philips Healthcare PDF, 82KB, File does not meet accessibility standards Date: 26. February 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 00530/15

Corrective action for various products for inhalation therapy, Teleflex Medical PDF, 499KB, File does not meet accessibility standards Date: 25. February 2015 Topics: Medical devices Type: Customer information

Product group Physical therapy - insufflation technique
Reference 00584/15

Corrective action for the Philips Allura FC, Philips Healthcare PDF, 310KB, File does not meet accessibility standards Date: 25. February 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for vascular diagnostics
Reference 00531/15

Corrective action for Troponin I-Check-1 device, VedaLab PDF, 307KB, File does not meet accessibility standards Date: 25. February 2015 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - immunological products
Reference 00604/15

Corrective action for the MultiDiagnost Eleva II/TV systems, Philips Healthcare PDF, 29KB, File does not meet accessibility standards Date: 25. February 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 00522/15

Urgent Safety Notice for the Trophy IRIX scissor arm of the Trophy IRIX Intra-oral X-Ray System, Carestream Dental PDF, 60KB, File does not meet accessibility standards Date: 25. February 2015 Topics: Medical devices Type: Customer information

Product group Radiological technology - radiological equipment for stomatological diagnostics
Reference 07183/14