Packaging for terminally sterilized medical devices - Sealable pouches and reels of porous and plastic film construction. Requirements and test methodsBS EN 868 5: 2009 Packaging for terminally sterilized medical devices. Sealable pouches and reels of porous and plastic film construction. Requirements and test methods Part 1 of the BS EN 868 series of European standards specifies general requirements and test methods for all packaging materials and systems intended for use as packaging for medical devices which are to be terminally sterilized in their packaging. BS EN 868 5 provides examples of

NOTE 1 This standard does not cover agricultural uses (see BS 5502)

It is proposed that future parts of ISO/IEC 27033 will address the following topics

Service contracts between customers and the service provider

It specifies performance requirements and basic safety for areas such as temperature and oxygen control

Although primarily intended for electrotechnical products this publication is not restricted to them and may be used in other fields where desired

that specifies the tolerances on dimensions and form for aluminium and aluminium alloy extruded round bars having diameters in the range from 8 mm up to 320 mm

8 Application of security glazing – Windows and doors

changing units

Manufacturers are encouraged to incorporate the small bore connectors specified in this series of Standards into medical devices or systems

12 Cybersecurity controls

Government bodies

BS EN 54-13:2005 specifies the requirements for compatibility and connectability assessment of system components that either comply with the requirements of BS EN 54 or with a manufacturer’s specification where there is no BS EN 54 standard