CSA Group Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices ISO 17664:2017

Description
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.
Description
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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Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices - ISO 17664:2017 - CSA Group
Toronto, Ontario, Canada
Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices
ISO 17664:2017
Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices ISO 17664:2017
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.

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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Technical Specifications

  CSA Group
Product Category Standards and Technical Documents
Product Number ISO 17664:2017
Product Name Processing of health care products - Information to be provided by the medical device manufacturer for the processing of medical devices
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