​All reusable equipment and instruments that are used in a skin penetration procedure must be cleaned and sterilised in a process that can be validated (the sterilising process can be checked) before they can be reused.

Note: select the link below to download and print this information as a poster to display at your skin penetration business.

Last updated: 01 September 2022
Download

Sterilisation of reusable equipment and instruments needs to be carried out in a separate reprocessing area, and in a way that minimises recontamination. A suggested layout is provided below

Figure 1: Suggested sterilisation area layout (AS/NZS 4815:2006)

diagram of a suggested sterilisation area layout for those operating a skin penetration business. Reproduced by NSW Health with

Cleaning

  • Used equipment must be placed in a separate part of the reprocessing area with all unclean equipment and instruments.
  • Place unclean equipment and instruments in the cleaning sink and rinse under warm water to remove all contaminants.
  • Clean equipment and instruments with a Therapeutic Goods Authority (TGA) approved detergent in warm water using a soft brush to minimise aerosols. Open equipment such as scissors and cuticle cutters and clean all surfaces.
  • Rinse equipment and instruments in warm running water and allow to dry in a drying cabinet or use a lint free cloth. Equipment and instruments should not be left to dry in the reprocessing area.
  • If an ultrasonic cleaner is used to clean equipment and instruments, the manufacturer’s instructions must be followed for its use.

Two gloved hands washing a bowl to ensure clean and sterile reuse of equipment and instrumentsTwo gloved hands washing a skin penetration instru in sopay water to ensure clean and sterile reuse of equipment and instruments

Packaging

  • Make sure instruments are completely dry before packaging.
  • Place each instrument by itself in a package that is large enough to open the instrument as far as possible so that steam can penetrate all surfaces of the instrument.
  • Seal the package and label the package with a water resistant felt-tipped pen. if you don’t know how to package instruments refer to the manufacturer’s instructions. Test indicators can be placed in packages to confirm that the autoclave has sterilised equipment
    and instruments.

Skin penetration instruments sealted in clear plasticAn autoclave is used to sterilise skin penetration instruments and equipment.

Sterilisation

  • Load the packages into the autoclave shelf in a single layer so they are not overlapping or touching the chamber walls. Several loads may be required for large amounts of equipment.
  • Keep to the sterilising procedure outlined in AS/NZS 4815:2006 Office-based health care facilities - Reprocessing of reusable medical and surgical instruments and equipment, and maintenance of the associated environment
  • Check the autoclave printout to make sure that the correct time, temperature and pressure levels were met.
  • Remove load and check that it is dry, the packaging is undamaged, and any test indicators have changed to the correct colour.

Skin penetration instruments sealed in plastic and placed on the shelves of an autoclave machine ready for sterilisationAn autoclave machine is used to sterilise skin penetration equipment and instruments so they can be reused.

Storage

  • Store sterilised instruments in a clean and dry area away from direct sunlight.
  • Only open the instrument packaging immediately before use.

Skin penetration equipment and utensils are stored in sealed plastic bags on a designated shelf. Skin penetration equipment and instruments sotred away rom direct sunight.

Records

  •  The autoclave must have a printout facility that shows:
    • the time and date when each article was sterilised; and
    • the length of time that the article was sterilised and the temperature and pressur+e levels of the benchtop autoclave.
  • The sterilisation records must be kept for 12 months and stored in a safe place that is easily available and can be reviewed by an authorised officer.

Further advice

Current as at: Thursday 1 September 2022
Contact page owner: Environmental Health