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BSI BS EN ISO 11607-1: Packaging for terminally sterilized medical devices Part 1: Requirements for materials, sterile barrier systems and packaging systems

Publication Date: Feb 28, 2010
SDO: BSI: British Standards Institution
 DOD Adopted   ANSI Approved Approved

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.

This part of ISO 11607 is applicable to industry, to health care facilities, and wherever medical devices are placed in sterile barrier systems and sterilized.

This part of ISO 11607 does not cover all requirements for sterile barrier systems and packaging systems for medical devices that are manufactured aseptically. Additional requirements might also be necessary for drug/device combinations.

This part of ISO 11607 does not describe a quality assurance system for control of all stages of manufacture.

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