Progressing Implementation to AS 5369:2023
August 19, 2024Transitioning from AS/NZS 4187:2014 to AS 5369:2023
The Guide can be accessed and viewed by clicking here.
About this document
This document supports health service organisations to implement the updated and new requirements in AS 5369:2023 Reprocessing of reusable medical devices and other devices in health and non-health related facilities.
Overview
Under Action 3.17a of the NSQHS Standards, health service organisations must ensure reprocessing practices align with relevant national and international standards and manufacturers’ guidelines.
In December 2023, AS 5369:2023 superseded:
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AS/NZS 4187:2014 Reprocessing of reusable medical devices in health service organisations, and
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AS/NZS 4815:2006 Office-based health care facilities – Reprocessing of reusable medical and surgical instruments and equipment, and maintenance of the associated environment.
AS 5369:2023 outlines the requirements for safe and effective reprocessing, storage, handling, and transport of reusable medical devices (RMDs) and other devices. It applies to all healthcare settings and to non-healthcare environments where RMDs or other devices are used.
Implementation considerations
Health service organisations should undertake a risk-based gap analysis to identify changes needed to comply with AS 5369:2023. They should also update or develop an asset management plan, including timelines for future redevelopment or upgrades to their reprocessing service, to meet the new standard’s requirements.
IntraSpace Compliance Service
IntraSpace offers AS 5369:2023 Compliance Service, contact us on 1800 800 573 or fill in our Compliance Service request form.
Read the IntraSpace guide here.











