Packaging for terminally sterilized medical devices - Sterilization wrap. Requirements and test methodsBS EN 868 2: 2009 Packaging for terminally sterilized medical devices. Sterilization wrap. Requirements and test methods BS EN 868 2 provides test methods and values for materials for 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 by the manufacturer and the user. BS EN 868 only introduces

BS EN 12620 specifies the properties of aggregates and filler aggregates obtained by processing natural

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Due to the general applicability of in vitro cytotoxicity tests and their widespread use in evaluating a large range of devices and materials

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Verification of the safety requirements and/or protective measures

EN 61000-4-2:1995

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The recommendations address the risk of ignition

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