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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 第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 | |
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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 | |
