Customer Service:
Mon - Fri: 8:30 am - 6 pm EST

 Historical

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 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.


Content Provider
International Organization for Standardization [iso]


Others Also Bought

Medical devices - Symbols to be used with medical device labels, labelling and information to be supplied - Part ...
Sterilization of health care products - Microbiological methods - Part 1: Determination of a population of microorganisms ...
Sterilization of health care products - General requirements for characterization of a sterilizing agent and the ...
Document History
Revises:
Revised By:
Included in Packages
This standard is not included in any packages.
Amendments & Corrections
We have no amendments or corrections for this standard.
ANSI Logo

As the voice of the U.S. standards and conformity assessment system, the American National Standards Institute (ANSI) empowers its members and constituents to strengthen the U.S. marketplace position in the global economy while helping to assure the safety and health of consumers and the protection of the environment.

CUSTOMER SERVICE
NEW YORK OFFICE
ANSI HEADQUARTERS