Packaging for terminally sterilized medical devices - Requirements for materials, sterile barrier systems and packaging systems Ingestion-build-115288

Packaging for terminally sterilized medical devices - Requirements for materials, sterile barrier systems and packaging systems Ingestion-build-115288What 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

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It provides a description of anthropometric measurements which can be used as a basis for comparing population groups and creating anthropometric databases

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This European Standard is applicable to all new pipeline systems and may be applied to modifications made to existing ones

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The specification includes recommendations for the following: construction and layout of facilities

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3 Terminology and definitions