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EN 868-5
Packaging for terminally sterilized medical devices-- Part 5: Sealable pouches and reels of porous materials and plastic film construction — Requirements and test methods
最终灭菌医疗器械包装材料 5部分:透气材料与塑料膜组成的可密封组合袋和卷材 要求和试验方法
送样规格
4.2.1多孔材料Porous material
4.2.2塑料膜Plastic film
4.2.2.1plastic film composite;
灭菌后外观The appearance of  plastic interply bond after the intended sterilization process(附录B)
送样规格:20pcs
4.2.2.2针孔pinholes(附录C) 送样规格:10pcs
4.2.2.3异物foreign matter and/or imperfections  送样规格:3pcs
4.2.2.5扯断因数Breaking factor(ASTM D882) 送样规格:20pcs(单边至少 15 cm)
4.5 Performance requirements and test methods
4.5.1密封强度Seal strength(附录D) 送样规格:灭菌前3pcs,灭菌后3pcs
4.5.2密封宽度 表面Seal width、surface (附录E) 送样规格:3pcs
4.5.3纤维取向the direction of the peel marked on the product(附录F) 送样规格:3pcs
4.6标识Marking 送样规格:1pcs
测试周期 Lead time: 14 working days


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