DIN EN 868-7-2009 最终灭菌医疗器械的包装.第7部分:低温消毒处理的粘合铜版纸.试验方法和要求.英文版本DIN EN 868-7-2009-09

标准号：DIN EN 868-7-2009
中文标准名称：*终灭菌医疗器械的包装.第7部分:低温消毒处理的粘合铜版纸.试验方法和要求.英文版本DIN EN 868-7-2009-09
英文标准名称：Packaging for terminally sterilized medical devices - Part 7: Adhesive coated paper for low temperature sterilization processes - Requirements and test methods; English version of DIN EN 868-7:2009-09
标准类型：C08
发布日期：1999/12/31 12:00:00
实施日期：1999/12/31 12:00:00
中国标准分类号：C08
国际标准分类号：11.080.30
引用标准：EN 20187;EN 20535;EN 21974;EN ISO 536;EN ISO 1924-2;EN ISO 2758;EN ISO 11607-1-2006;ISO 3689;ISO 3781;ISO 5636-3;ISO 6588-2-2005;ISO 8601;ISO 9197;ISO 9198
适用范围：This part of EN 868 provides test methods and values for sealable adhesive coated paper manufactured frompaper complying with EN 868-6, used as sterile barrier systems and/or packaging systems that are intendedto maintain sterility of terminally sterilized medical devices to the point of use. The materials specified in thispart are intended to be used for ethylene oxide or irradiation sterilization.NOTE 1 The need for a protective packaging may be determined by the manufacturer and the user.This part of EN 868 only introduces performance requirements and test methods that are specific to theproducts covered by this part of EN 868 but does not add or modify the general requirements specified inEN ISO 11607-1.As such, the particular requirements in 4.2 to 4.3 can be used to demonstrate compliance with one or morebut not all of the requirements of EN ISO 11607-1.NOTE 2 When additional materials are used inside the sterile barrier system in order to ease the organization, dryingor aseptic presentation (e.g. inner wrap, container filter, indicators, packing lists, mats, instrument organizer sets, trayliners or an additional envelope around the medical device) then other requirements, including the determination of theacceptability of these materials during validation activities, may apply.The materials specified in this part of EN 868 are intended for single use only.