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)

SIS-EN-ISO-17664 - 2017 EDITION - CURRENT
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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.

To find similar documents by classification:

11.080.01 (Sterilization and disinfection in general Including sterilization methods, air quality of surgery rooms, etc.)


Medical devices

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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)