Packaging for terminally sterilized medical devices - Requirements for materials, sterile barrier systems and packaging systemsWhat is this standard about? This part of ISO 11607 specifies the requirements and test methods for materials, preformed sterile barrier systems, sterile barrier systems and packaging systems that are intended to maintain sterility of terminally sterilized medical devices until the point of use. Who is this standard for? This part of ISO 11607 is applicable to industry, to health care facilities, and wherever medical devices are placed in sterile

BS EN 13429:2004 provides a framework within which this and four other standards (BS EN 13427

A major role is the prevention of product damage and/or product waste

The test methods reported in this document are intended for commercial testing applications and can also be adopted as benchmark methods for scientific research

BS EN 13975 outlines the sampling procedure requirements for acceptance testing of finished in vitro diagnostic medical devices

BS 8409 is an important standard to improve safety records and reduce risks in indoor play areas for children

particularly the preparation of samples

indicate a value of the mechanical strength coefficient of the welded joint for each welding process

marine organisms

It covers characteristics that are of importance for trade

It also covers other aspects of design and safety measures for the base isolation of buildings

Determination of the percentage yield point extension

Provisions for maintainability