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ANSI/AAMI/ISO 17665-1:2006/(R)2013

Sterilization of health care products—Moist heat—Part 1 Requirements for the development, validation and routine control of a sterilization process for medical devices

Summary

This document specifies requirements for the development, validation, and routine control of a moist heat sterilization process for medical devices used in any facility that manufactures or reprocesses medical devices. Annex 2

Technical characteristics

Publisher Association for the Advancement of Medical Instrumentation (AAMI)
Publication Date 01/01/2006
Confirmation Date 01/01/2013
Page Count 0
Themes Sterilization—Industrial
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