scope:

This International Standard specifies the requirements for single-use materials and reusable containers used for packaging of terminally sterilized medical devices, whether produced industrially or in health care facilities (see clause 6). This International Standard outlines principal requirements for packaging process development and validation for the manufacturer of terminally sterilized medical devices (see clause 7). Forming and sealing are considered to be the most critical processes. Other process operations that can affect the final package are addressed also. Guidelines are provided for the most common practices and techniques. This International Standard specifies requirements for essential criteria used to evaluate the performance of packages for sterile medical devices (see clause 7). The intent is to provide designers and manufacturers of medical devices with a framework of laboratory tests and evaluations that can be used to qualify the overall performance of the package used to protect device components during handling, distribution and storage.