Packaging for terminally sterilized medical devices - Paper for low temperature sterilization processes. Requirements and test methodsBS EN 868 6: 2009 Packaging for terminally sterilized medical devices. Paper for low temperature sterilization processes. Requirements and test methods BS EN 868 Part 6 provides test methods and values for paper used in the manufacture of preformed sterile barrier systems and or packaging systems that are intended to maintain sterility of terminally sterilized medical devices to the point of use. The need for a protective packaging may be determined

Quality control department

a part of the BS EN 10277 series

- Non-sterile

BS EN 61340-5-1 provides the requirements for an ESD control program

Melting process

Temper designations

This standard specifies requirements and a procedure by which a person or organization responsible for placing packaging or packed product on the market (the supplier) may combine the application of the five packaging standards

Measuring the percentage elongation after fracture if the specified value is less than 5 %

transparent way

and developer of technical drawings

BS EN ISO 9004:2009

Section 2 describes the site and geotechnical data that is required together with material properties