SIS-EN-ISO-17664 › Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices (ISO 17664:2017)
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ISO 17664:2017 specifies 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. This includes information for processing prior to use or reuse of the medical device. The provisions of ISO 17664:2017 are applicable to medical devices that are intended for invasive or other direct or indirect patient contact.
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Designation Name
SS-EN ISO 17664:2017
Revision Level
2017 EDITION
Status
Current
Publication Date
Dec. 14, 2017
Language(s)
English
Page Count
40
International Equivalent
EN ISO 17664:2017(IDT); ISO 17664:2017(IDT)