Regulation of single use devices

• Definitions relating to the regulation of the re-manufacture of single use medical devices
  <http://www.tga.gov.au/devices/sud-definitions.htm>
• Restocking and sterilisation of non-sterile single-use implants for use in orthopaedic procedures
  <http://www.tga.gov.au/devices/sudprocedures.htm>
• Guidance regarding the re-manufacture of single use medical devices for reuse
  <http://www.tga.gov.au/devices/fs-sudguid.htm>
• FAQ on regulation of the re-manufacture of single use medical devices (SUDs)
  <http://www.tga.gov.au/devices/sudfaq.htm>
• Re-manufacturing single use medical devices
  <http://www.tga.gov.au/devices/fs-sudman.htm>
• Regulation of the re-manufacture of single use medical devices (SUDs)
  <http://www.tga.gov.au/devices/sudreg.htm>

Updates on the regulation of the re-manufacture of single use medical devices

• October 2006 update on the regulation of the re-manufacture of single use medical devices
  <http://www.tga.gov.au/devices/sudupd0610.htm>
• November 2005 update on the regulatory framework for the re-manufacture of single use medical devices for reuse
  <http://www.tga.gov.au/devices/sudtrans.htm>