中華人民共和國國家標準(中國大陸GB標準)英文版

GB標準是中華人民共和國國家標準，也叫GB國標，是中國大陸強制執行的國家標準，所有中國大陸境內銷售的商品及提供服務都必須符合GB國家標準的要求，包括進口商品及服務；本網站提供GB國家標準的查詢檢索，英文版翻譯，GB標準產品檢測檢驗及合規性分析服務；


	YY/T 0698.5—2023 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（中英文版） 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
	YY/T 0698.2-2022 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（中英文版） Packaging materials for terminally sterilized medical devices - Part 2: Requirements and test methods for packaging materials for sterilization
	YY/T 0681.4—2021 无菌医疗器械包装试验方法第4部分：染色液穿透法测定透气包装的密封泄漏（中英文版） Test methods for sterile medical device packaging - Part 4: Determination of seal leakage of breathable packaging by dye penetration method
	GB/T 39690.2-2020 塑料源自柔性和刚性消费品包装的聚丙烯（PP）和聚乙烯（PE）回收混合物第2部分：试样制备和性能测定（中英文版） Plastics—Mixtures of polypropylene (PP) and polyethylene (PE) recyclate derived from PP and PE used for flexible and rigid consumer packaging—Part 2：Preparation of test specimens and determination of properties
	YY/T 1432-2016 通过测量热封试样的密封强度确定医疗器械软性包装材料的热封参数的试验方法（中英文版） (Test methods for sealing parameters flexible packaging materials for medical devices is determined by measuring the heat-sealing strength of the sample)
	GB/T 19633.2-2015 最终灭菌医疗器械包装第2部分：成形、密封和装配过程的确认的要求（中英文版） Packaging for terminally sterilized medical devices—Part 2: Validation requirements for forming, sealing and assembly processes
	GB/T 19633.1-2015 最终灭菌医疗器械包装第1部分：材料、无菌屏障系统和包装系统的要求（中英文版） Packaging for terminally sterilized medical devices?aPart 1: Requirements for materials, sterile barrier systems and packaging systems
	YY/T 0681.11-2014 无菌医疗器械包装试验方法第11部分:目力检测医用包装密封完整性（中英文版） Test methods for sterile medical device package. Part 11: Determining integrity of seals for medical packaging by visual inspection
	YY/T 0698.1-2011 最终灭菌医疗器械包装材料第1部分：吸塑包装共挤塑料膜要求和试验方法（中英文版） Packaging materials for terminal sterilized medical devices. Part 1: Co-extrusion plastic films used for vacuum forming packaging. Requirements and test methods
	SN/T 3062.3-2011 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（中英文版） 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
	SN/T 3006-2011 包装材料用油墨中有机挥发物的测定气相色谱法（中英文版） Determination of volatile organic compouds in printing inks used for packaging materials. Gas chromatography method
	SN/T 3062.2-2011 进口医疗器械灭菌包装第2部分：纸袋-要求和试验方法（中英文版） Packaging materials for terminally sterilized medical devices for import. Part 2: Paper bags. Requirements and test methods
	SN/T 3062.4-2011 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（中英文版） Packaging materials for terminally sterilized medical devices for import. Part 4: Requirements for materials and sterile barrier systems of importing medical device sterilization packaging
	SN/T 3061-2011 进口医疗器械灭菌包装检验操作规程（中英文版） Rules of the inspection of packaging for import terminally sterilized medical devices
	YY/T 0698.2-2009 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（中英文版） Packaging materials for terminal sterilized medical devices. Part 2: Sterilization wrap. Requirements and test methods
	YY/T 0698.5-2009 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（中英文版） Packaging materials for terminal sterilized medical devices. Part 5: Heat and self-sealable pouches and reels of paper and plastic film construction. Requirements and test methods
	YY/T 0698.10-2009 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（中英文版） 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
	YY/T 0698.4-2009 最终灭菌医疗器械包装材料第4部分：纸袋要求和试验方法（中英文版） Packaging materials for terminal sterilized medical devices. Part 4: Paper bags. Requirements and test methods
	YY/T 0698.6-2009 最终灭菌医疗器械包装材料第6部分：用于低温灭菌过程或辐射灭菌的无菌屏障系统生产用纸要求和试验方法（中英文版） Packaging materials for terminal sterilized medical devices. Part 6: Paper for manufacture of sterile barrier systems intended for sterilization by low temperature sterilization processes or irradiation. Requirements and test methods
	YY/T 0698.8-2009 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（中英文版） Packaging materials for terminally sterilized medical devices. Part 8: Re-usable sterilization containers for team sterilizers. Requirements and test methods

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