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ISO 11137 - Sterilization of Health Care Products Package

ISO 11137-1, ISO 11137-2 and ISO 11137-3

The ISO 11137 - Sterilization of Health Care Products Package provides the requirements for developing, validating and routinely controlling the sterilization process of medical devices. In addition to providing the requirements for the sterilization process of medical devices, this package also considers the products' environment, personnel and their hygiene, packaging / storage, sterilization doses and more to inactivate microbiological contaminants on medical devices. This package is reduce by 25% off of the standard list price and includes the following ISO Standards: ISO 11137-1:2006, ISO 11137-1:2006/Amd1:2013, ISO 11137-2:2013 and ISO 11137-3:2017.

ISO 11137 - Sterilization of Health Care Products Package includes:


Content Provider
International Organization for Standardization [ISO]


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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.

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