GB/T 47144-2026

This document specifies the requirements for the development, validation, and routine control of the cleaning process for medical devices.
This document applies to the cleaning process during the production and use of medical devices, and medical institutions and other medical products requiring cleaning may refer to it for implementation.
This document does not apply to: — Disposable medical devices supplied in a ready-to-use state for patient use; — Textiles used in patient sterile drape systems or surgical gowns; or — Devices that may come into contact with prions, such as devices that may be contaminated with the transmissible spongiform encephalopathy (TSE) virus.