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15,001 results

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Recall of the Instrument Set for the Lubinus SPII Anatomically Adapted Hip Prosthesis System, Waldemar Link GmbH PDF, 180KB, File does not meet accessibility standards Date: 13. September 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 04191/12, 04192/12, 04193/12

Recall of all lots for the DUET TRS Universal Straight und Articulating Single Use Loading Units, Covidien PDF, 1,012KB, File does not meet accessibility standards Date: 13. September 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - general instruments
Reference 05544/12

Safety Notice for the product "Neue Ulmer Hüftorthese", Nea Tec PDF, 35KB, File does not meet accessibility standards Date: 12. September 2012 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology - orthoses
Reference 04152/11

Recall for the Gliding Nail GN Blade Handle, Smith & Nephew Orthopaedics PDF, 49KB, File does not meet accessibility standards Date: 12. September 2012 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans - bone surgery
Reference 05769/12

Safety Notice for the Chrystal LT 201 X-ray system from the manufacturer XCAN AG, MTS Maschinenbau AG PDF, 73KB, File does not meet accessibility standards Date: 12. September 2012 Topics: Medical devices Type: Customer information

Product group Radiological technology - stationary radiological equipment
Reference 04547/12

Lot Recall for the Twinplusdrain drainage catheter, Peter Pflugbeil GmbH PDF, 652KB, File does not meet accessibility standards Date: 12. September 2012 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis - drainages and suction systems
Reference 05722/12

Safety Notice concerning the FreeSpan™ Traverse and FreeSpan Ultra Twin™ Traverse, Liko AB PDF, 696KB, File does not meet accessibility standards Date: 11. September 2012 Topics: Medical devices Type: Customer information

Product group General equipment for medical treatment - ward equipment and equipment for emergency medical services
Reference 04013/12

Safety Notice concerning the Flex Large 4 coil for Magnetom Skyra, Verio, Spectra and Biograph mMR systems PDF, 406KB, File does not meet accessibility standards Date: 11. September 2012 Topics: Medical devices Type: Customer information

Product group Electromedical fields - equipment for MR tomography
Reference 05718/12

Lot Recall for the “Achsstielknie” prosthesis, AQ Implants GmbH PDF, 58KB, File does not meet accessibility standards Date: 11. September 2012 Topics: Medical devices Type: Customer information

Product group Non-active implants - bone surgery
Reference 05568/12

Safety Notice for the physical exercise Genius ECO body tension, Frei AG PDF, 217KB, File does not meet accessibility standards Date: 11. September 2012 Topics: Medical devices Type: Customer information

Product group Physical therapy - massage / mobility devices
Reference 01027/12