Standard Code | Standard Title | Standard Class | Order |
---|---|---|---|
YY/T 0698.5—2023 |
Packaging materials for terminally sterilized medical devices Part 5: Sealable combination bags and rolls composed of breathable materials and plastic films Requirements and test methods {译} 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 |
China Pharmaceutics Industry
Standards terminally |
English PDF |
YY/T 0698.2-2022 |
Packaging materials for terminally sterilized medical devices - Part 2: Requirements and test methods for packaging materials for sterilization {译} 最终灭菌医疗器械包装材料 第2部分:灭菌包裹材料 要求和试验方法 |
China Pharmaceutics Industry
Standards terminally |
English PDF |
SN/T 3062.4-2011 |
Packaging materials for terminally sterilized medical devices for import. Part 4: Requirements for materials and sterile barrier systems of importing medical device sterilization packaging 进口医疗器械灭菌包装 第4部分:材料和预成型无菌屏障系统要求 |
China Import Export Inspection
Standards terminally |
English PDF |
SN/T 3062.3-2011 |
Packaging materials for terminally sterilized medical devices for import. Part 3: Sealable pouches and reels of porous materials and plastic film construction. Requirements and test methods 进口医疗器械灭菌包装 第3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 |
China Import Export Inspection
Standards terminally |
English PDF |
SN/T 3062.2-2011 |
Packaging materials for terminally sterilized medical devices for import. Part 2: Paper bags. Requirements and test methods 进口医疗器械灭菌包装 第2部分:纸袋-要求和试验方法 |
China Import Export Inspection
Standards terminally |
English PDF |
SN/T 3062.1-2011 |
Packing materials for terminally sterilized medical devices for import. Part 1: Validation requirements for forming,sealing and assembly processes 进口医疗器械灭菌包装 第1部分:成形、密封和装配过程的确认要求 |
China Import Export Inspection
Standards terminally |
English PDF |
SN/T 3061-2011 |
Rules of the inspection of packaging for import terminally sterilized medical devices 进口医疗器械灭菌包装检验操作规程 |
China Import Export Inspection
Standards terminally |
English PDF |
YY/T 0698.9-2009 |
Packaging materials for terminally sterilized medical devices. Part 9: Uncoated nonwoven materials of polyolefines for use in the manufacture of sealable pouches, reels and lids. Requirements and test methods 最终灭菌医疗器械包装材料 第9部分:可密封组合袋、卷材和盖材生产用无涂胶聚烯烃非织造布材料 要求和试验方法 |
China Medicine & Medical Device
Standards terminally |
English PDF |
YY/T 0698.8-2009 |
Packaging materials for terminally sterilized medical devices. Part 8: Re-usable sterilization containers for team sterilizers. Requirements and test methods 最终灭菌医疗器械包装材料 第8部分:蒸汽灭菌器用重复性使用灭菌容器 要求和试验方法 |
China Medicine & Medical Device
Standards terminally |
English PDF |
YY/T 0698.10-2009 |
Packaging materials for terminally sterilized medical devices. Part 10: Adhesive coated nonwoven materials of polyolefines for use in the manufacture of sealable pouches, reels and lids. Requirements and test methods 最终灭菌医疗器械包装材料 第10部分:可密封组合袋、卷材和盖材生产用涂胶聚烯烃非织造布材料 要求和试验方法 |
China Medicine & Medical Device
Standards terminally |
English PDF |
YY/T 0615.1-2007 |
Requirements for medical devices to be designated “STERILE”. Part 1: Requirements for terminally sterilized medical devices 标示无菌医疗器械的要求第1部分:最终灭菌医疗器械的要求 |
China Medicine & Medical Device
Standards terminally |
English PDF |
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