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14,972 results

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Corrective Action for Dimension RxL – Reagent Management System (RMS) Power Cord Plug, Siemens PDF, 209KB, File does not meet accessibility standards Date: 07. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04718/12

Corrective Action for ABL800 and ABL700, Radiometer PDF, 25KB, File does not meet accessibility standards Date: 07. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04808/12

Safety Notice concerning shifted Dose for XiO Proton Spot Beams, Elekta PDF, 119KB, File does not meet accessibility standards Date: 07. August 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - radiotherapy treatment planning systems
Reference 03756/12

Safety Notice for EndoWrist Hot Shears™ instruments, Intuitive Surgical® PDF, 272KB, File does not meet accessibility standards Date: 07. August 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - surgical equipment
Reference 04624/12

Safety Notice for the Portnoy Ventricular Catheter, Integra NeuroSciences PDF, 87KB, File does not meet accessibility standards Date: 06. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 05048/12

Lot Recall for Optipac Refobacin Bone Cement R, BIOMET PDF, 81KB, File does not meet accessibility standards Date: 06. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - materials for implants
Reference 04819/12

Urgent Safety Notice for syngo.plaza, Siemens Healthcare PDF, 512KB, File does not meet accessibility standards Date: 06. August 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - auxiliary equipment and supplies for radiology / nuclear medicine
Reference 04703/12

Lot Recall for Calistar A and Calistar P, Promedon S.A. PDF, 42KB, File does not meet accessibility standards Date: 06. August 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - special implants
Reference 04221/12

Corrective Action for Dimension Vista HCYS Flex Reagent Cartridge, Siemens Healthcare PDF, 25KB, File does not meet accessibility standards Date: 06. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04664/12

Important Information Update regarding Eon model 65-3716, Eon Mini model 65-3788 and Brio model 65-6788, St. Jude Medical PDF, 76KB, File does not meet accessibility standards Date: 03. August 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 05919/11

Corrective Action for ABL 90 FLEX, Radiometer PDF, 21KB, File does not meet accessibility standards Date: 03. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - equipment / products for clinical chemistry
Reference 04451/12

Safety Notice concerning MR290 Autofeed Humidification Chambers, Fisher & Paykel PDF, 55KB, File does not meet accessibility standards Date: 03. August 2012 Topics: Medical devices Type: Customer information

Product group Surgical equipment/ Anaesthesia - anaesthesia and medical gas supply
Reference 05042/12

Safety Corrective Action regarding Eon Mini model 65-3788 and Brio model 65-6788, St. Jude Medical PDF, 74KB, File does not meet accessibility standards Date: 03. August 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - biostimulators
Reference 04939/12

Safety Notice for the Brilliance series 6, 16, 40, 64, CT Big Bore, iCT and iCT SP CT systems, Philips Healthcare PDF, 85KB, File does not meet accessibility standards Date: 02. August 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - CT scanners
Reference 04978/12

Corrective Action for Techno TwinStation, Bio-Rad PDF, 657KB, File does not meet accessibility standards Date: 02. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - haematological, histological and cytological products
Reference 04019/12

Safety Notice for the EVG Videogastroskop ENDOMED-DUO and EVC 21-37 Videocoloskop ENDOMED-DUO, ESCAD PDF, 75KB, File does not meet accessibility standards Date: 02. August 2012 Topics: Medical devices Type: Customer information

Product group Optics / Precision engineering - endoscopes
Reference 01352/12

Recall for the sterile Teflon Tube T2 Humerus, Stryker Osteosynthesis PDF, 60KB, File does not meet accessibility standards Date: 02. August 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04983/12

Safety Corrective Action regarding EXCOR arterial cannula with graft CGRG-021, Berlin Heart GmbH PDF, 1MB, File does not meet accessibility standards Date: 02. August 2012 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices - artificial hearts
Reference 05000/12

Corrective action for BacT/Alert, BioMerieux PDF, 319KB, File does not meet accessibility standards Date: 01. August 2012 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics - microbiological products
Reference 01925/12

Recall of VariSource™ IX and 200 series Nucletron Adapter and Transfer Guide Tube and Set, Varian medical systems PDF, 1MB, File does not meet accessibility standards Date: 01. August 2012 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection - nuclear medical therapeutic equipment
Reference 02518/12