BfArM - Federal Institute for Drugs and Medical Devices

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Recall of Surgical Instrumentkit for THA with „Unique“ customized femoral stem from Scandinavian Customized Prosthesis PDF, 58KB, File does not meet accessibility standards Date: 14. July 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01547/06

Exchanges in artificial feet from College Park Industries PDF, 58KB, File does not meet accessibility standards Date: 11. July 2006 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 02386/04

Information for the hand-driven bike model Shark from Sunrise Medical PDF, 148KB, File does not meet accessibility standards Date: 11. July 2006 Topics: Medical devices Type: Customer information

Product group Orthopaedic / Rehabilitation technology
Reference 01758/06

Recall of the SynchroMed EL implantable programmable pumps from Medtronic PDF, 61KB, File does not meet accessibility standards Date: 07. July 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01278/06

Information for the LAP Dorado Laser System PDF, 47KB, File does not meet accessibility standards Date: 07. July 2006 Topics: Medical devices Type: Customer information

Product group Radiotherapy / Radiation protection
Reference 01512/06

Corrective action and recall of FreeStyle Mini, FreeStyle Freedom and Freestyle from Abbott PDF, 303KB, File does not meet accessibility standards Date: 07. July 2006 Topics: Medical devices Type: Customer information

Product group In-vitro diagnostics
Reference 01551/06

Information for the use of Hem-o-lok large clip from Teleflex PDF, 260KB, File does not meet accessibility standards Date: 06. July 2006 Topics: Medical devices Type: Customer information

Product group Medical instruments for use in humans
Reference 01589/06

Information for the CADD-Legacy Duodopa Pump, Model 1400 from Smiths Medical PDF, 24KB, File does not meet accessibility standards Date: 06. July 2006 Topics: Medical devices Type: Customer information

Product group Injections / Infusions / Transfusions / Dialysis
Reference 01518/06

Information for the INSIGNIA and NEXUS pacemakers from Guidant PDF, 260KB, File does not meet accessibility standards Date: 06. July 2006 Topics: Medical devices Type: Customer information

Product group Active implantable medical devices
Reference 01794/06

Recall of the biopsy instruments Fischer Cone Biopsy Excisor from Apple PDF, 47KB, File does not meet accessibility standards Date: 05. July 2006 Topics: Medical devices Type: Customer information

Product group Medical electronics / Electromedical devices
Reference 01116/06