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ISO 17664:2017 Preview
Processing of health care products -- Information to be provided by the medical device manufacturer for the processing of medical devices
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.
General information
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Status : PublishedPublication date : 2017-10
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Edition : 2Number of pages : 24
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- ICS :
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Sterilization and disinfection in general
Buy this standard
| Format | Language | |
|---|---|---|
| PDF + ePub | ||
| Paper |
- CHF118
Life cycle
A standard is reviewed every 5 years
Revisions / Corrigenda
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Previously
ISO 17664:2004
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Now
ISO 17664:2017
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