ANSI/AAMI/ISO 17664:2017

Glossary of equivalent standards
Committee representation
Background of ANSI/AAMI adoption of
 ISO 17664:2017
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 Validation of the processes identified in
  the information provided by the medical
  device manufacturer
5 Risk analysis
6 Information to be provided by the
  medical device manufacturer
7 Presentation of the information
Annex A (informative) - Commonly utilized
        processing methods
Annex B (informative) - Example of processing
        instructions for reusable medical devices
Annex C (informative) - Classification of medical
        devices
Annex D (informative) - Additional guidance on
        information to be provided by the medical
        device manufacturer
Bibliography

Describes requirements for the information to be provided by the medical device manufacturer for the processing of a medical device that requires cleaning followed by disinfection and/or sterilization to ensure that the device is safe and effective for its intended use.