ISO/AWI TS 17664-3

Тезис

This document gives guidance how to define the cleaning requirements of a reusable medical device by use of a quantitative cleaning classification system that allows designation to a product family. Medical device design features, material of construction and intended patient use are used as attributes for device classification and are used to designate processing parameters for cleaning. Guidance is provided for the designation of a master product within a product family. The quantitative cleaning classification system is comprised of two parts: i) classification of reusable medical devices ii) classification of manual and or automated cleaning processes suitable for the cleaning classification assigned to a reusable medical device This allows grouping of reusable medical devices into product families during routine processing and identification of master products during cleaning validation.