10. Reprocessing of reusable medical devices and other devices in general practice

Classification for reprocessing devices


      1. Classification for reprocessing devices

Last revised: 12 Jun 2026

Classification for reprocessing devices

The Spaulding Classification Scheme categorises reusable medical devices based on their risk of infection transmission, and the necessary level of reprocessing required before reuse. Table 10.2 provides general criteria for the reprocessing and storage of reusable medical devices in general practice based on the Spaulding Classification.

In general practice, most devices are semi-critical or non-critical, as procedures are typically non-invasive or minimally invasive. Critical devices, which come into contact with sterile body tissues or the vascular system, are rarely used in general practice. The specific requirements for reprocessing critical devices are not included in this section. For detailed guidance on critical devices, refer to AS 5369 – Reprocessing of reusable medical devices and other devices in health and non-health related facilities.

Table 10.2 General criteria for reprocessing and storage of reusable medical devices

Level of risk

Process

Storage

Non-critical medical device

A medical device that comes into contact with intact skin but not mucous membranes

 

Clean as soon as possible after using

For further treatment, disinfect with compatible low-level or intermediate-level instrument grade disinfectant or thermal disinfection

Note: Some non-critical medical devices might not come into direct contact with a patient, eg a kidney dish or bowl. However, as the item is used within the patient environment there is potential for the item to become contaminated

Store in a clean, dry place to minimise environmental contamination

Semi-critical medical device

A medical device that comes into contact with mucous membranes or non-intact skin

Clean using a washer-disinfector as soon as possible after using

Sterilise by moist heat after cleaning

Manual and ultrasonic cleaning of reusable medical devices is only acceptable if the device’s validated cleaning instructions require manual cleaning or ultrasonic cleaning, or as a pre-treatment prior to cleaning in a washer-disinfector

Store to prevent environmental contamination in a designated storage system (e.g. dedicated clean cupboard or drawer, or a controlled environment drying cabinet)

Critical medical device

A medical device that is intended to be introduced directly into or have contact with the vascular system or normally sterile areas of the body

Note: A critical medical device contaminated with microorganisms confers a high risk of transmission of infectious agents

Pre-clean as above

If a reusable medical device is heat or moisture sensitive, sterilise using an alternative low-temperature sterilisation process

Refer to AS 5369 – Reprocessing of reusable medical devices and other devices in health and non-health related facilities

Sterility needs to be maintained

Integrity of the package needs to be maintained

Needs to be protected from environmental contamination and stored in a designated storage area

Reusable medical devices processed through a liquid chemical sterilisation process to be used immediately

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