DIN EN 868-6-2009 最终灭菌医疗器械的包装.第6部分:低温灭菌处理用纸.试验方法和要求.英文版本DIN EN 868-6-2009-09

标准号：DIN EN 868-6-2009
中文标准名称：*终灭菌医疗器械的包装.第6部分:低温灭菌处理用纸.试验方法和要求.英文版本DIN EN 868-6-2009-09
英文标准名称：Packaging for terminally sterilized medical devices - Part 6: Paper for low temperature sterilization processes - Requirements and test methods; English version of DIN EN 868-6:2009-09
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 paper used in the manufacture of preformed sterilebarrier systems and/or packaging systems that are intended to maintain sterility of terminally sterilized medicaldevices to the point of use.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.Paper specified in this part of the series EN 868 is intended for use in part or complete manufacture ofpouches and form and fill packs and lidding material for packs.NOTE 2 The paper specified in this part of the series EN 868 is suitable for the manufacture of sterile barrier systemsto be used in ethylene oxide, irradiation or low temperature steam formaldehyde sterilization processes and to producecoated paper according to EN 868-7.NOTE 3 Paper according to EN 868-3 can also be used for these sterilization processes.The materials specified in this part of EN 868 are intended for single use only.NOTE 4 When additional materials are used inside the sterile barrier system in order to ease the organization, dryingor aseptic presentation (e.g. inner wrap, container filters, 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.