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Microsoft Word - Decontamination of Re-usable Medical Devices

Microsoft Word - Decontamination of Re-usable Medical Devices

Microsoft Word - Decontamination of Re-usable Medical

HPSS Controls Assurance Standard Decontamination of Re-usable Medical Devices STANDARD DECONTAMINATION OF RE-USABLE MEDICAL DEVICES There is a system in place that ensures as far as reasonably practicable that all reusable medical devices are properly decontaminated prior to use and that the risks associated with decontamination facilities and processes are adequately managed. OVERVIEW The decontamination of re-usable medical devices is the combination of processes, which if not correctly undertaken, individually or collectively, may increase the likelihood of infectious agents being transferred to individuals, or the environment. The re-usable medical device life cycle comprises the following processes - acquisition, cleaning, disinfection, inspection, disposal, packaging, sterilization, transportation, and storage before use. This cycle is used to render a re-usable item safe for further use. In this standard, the term reusable medical device applies to all such devices whether owned by the organisation, rented, on loan or acquired by any other means. Re-Usable Medical Device Life Cycle Figure 1 The decontamination process is required to make medical devices: • Safe for users to handle • Safe for use on the patient ACQUISITION 1. Purchase 2. Loan CLEANING At all stages: Location Facilities Equipment Management Policies/Procedures DISINFECTION The Microbiology Advisory Committee to the Department of Health (MAC Manual), Sterilization, Disinfection, and Cleaning of Medical Equipment: Guidance on © Crown Copyright 2004 Version November 2004 USE STORAGE TRANSPORT TRANSPORT STERILIZATION INSPECTION PACKAGING DISPOSAL 1. Scrap 2. Return to lender Page 1 of 42

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