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SN/T 3062的本部分规定了用于灭菌医疗器械包装的密封袋和卷材的试验方法和要求。 本部分的主要目的是为菌屏障或包装系统建立起相应标准以保证灭菌的医疗器械的菌状态。 本部分规定的所有器械均为一次性使用
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
YY/T 0698的本部分提供了适用于最终灭菌医疗器械包装的涂胶层聚烯烃非织造布材料的要求和试验方法。 本部分未对ISO 11607-1的通用要求增加要求。因此，4.2~4.3中的专用要求可用以证实符合ISO 11607-1的一项或多项要求，但不是其全部要求。 本部分所规定的材料预期部分或全部
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
YY/T 0698 的本部分提供了适用于最终灭菌医疗器械包装的涂胶聚烯烃非织造布材料的要求和 试验方法。 本部分未对 ISO 11607-1 的通用要求增加要求。因此，4. 2一4. 3 中的专用要求可用以证实符合 ISO 11607-1 的一项或多项要求 ，但不是其全部要求。 本部分所规定的材料
This part of the series of EN 868 provides examples of particular requirements and test methods for heat and self-sealable pouches and reels
Packaging materials and systems for medical devices which are to be sterilized - Heat and self-sealable pouches and reels of paper and plastic film construction - Requirements and test methods
This part of the series of EN 868 provides examples of particular requirements and test methods for heat and self-sealable pouches and reels
Packaging materials and systems for medical devices which are to be sterilized - Heat and self-sealable pouches and reels of paper and plastic film construction - Requirements and test methods
本标准对用于包装后面有微生物要求非菌兽药粉剂、可溶性粉剂、散剂、预混剂、颗粒剂、片剂等固体制剂的塑料与铝箔复合膜和复合袋的定义和术语、技术要求、试验方法、检验规则、标志、标签和随行文件、包装、运输和贮存等进行规范。 1）按照本标准条款要求，组织实施了重要试验项目的验证，实施的试验项目有：复合袋
This part of EN 868 provides test methods and values for sealable pouches and reels manufactured from porous materials complying with either EN 868
Packaging for terminally sterilized medical devices - Part 5: Sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods
This document specifies test methods and values for sealable pouches and reels manufactured from porous materials complying with either EN 868 part 2@
Packaging for terminally sterilized medical devices - Part 5: Sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods
Packaging for terminally sterilized medical devices - Part 5 : sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods.
Sealing Cartridge For Two Component Materials
Schv?lení ST SEV 4769 34 dopni uěilu ministeustvo ?kolství ?SR. Zpracovatel: F?ikullíi slrnjní ?eského vysokého u?eni teehnick?ho v Praze, Dne
Representation of seals on nssembly drawings
This notice should be filed in front of, MIL-S-38714B(USAF) dated 15 May 1987
SEALING CARTRIDGE FOR TWO COMPONENT MATERIALS
and similar materials. This specification covers cartridges which are used to store, mix and apply sealants, adhesives
SEALING CARTRIDGE FOR TWO COMPONENT MATERIALS
Packaging materials and systems for medical devices which are to be sterilized Part 5: Heat and self-sealable pouches and reels of paper and plastic film construction Requirements and test methods Incorporating corrigendum October 2001
SN/T 3062的本部分规定了用于灭菌医疗器械包装的密封袋和卷材的试验方法和要求。 本部分的主要目的是为菌屏障或包装系统建立起相应标准以保证灭菌的医疗器械的菌状态。 本部分规定的所有器械均为一次性使用
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
YY/T 0698的本部分提供了适用于最终灭菌医疗器械包装的涂胶层聚烯烃非织造布材料的要求和试验方法。 本部分未对ISO 11607-1的通用要求增加要求。因此，4.2~4.3中的专用要求可用以证实符合ISO 11607-1的一项或多项要求，但不是其全部要求。 本部分所规定的材料预期部分或全部
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
YY/T 0698 的本部分提供了适用于最终灭菌医疗器械包装的涂胶聚烯烃非织造布材料的要求和 试验方法。 本部分未对 ISO 11607-1 的通用要求增加要求。因此，4. 2一4. 3 中的专用要求可用以证实符合 ISO 11607-1 的一项或多项要求 ，但不是其全部要求。 本部分所规定的材料
This part of the series of EN 868 provides examples of particular requirements and test methods for heat and self-sealable pouches and reels
Packaging materials and systems for medical devices which are to be sterilized - Heat and self-sealable pouches and reels of paper and plastic film construction - Requirements and test methods
This part of the series of EN 868 provides examples of particular requirements and test methods for heat and self-sealable pouches and reels
Packaging materials and systems for medical devices which are to be sterilized - Heat and self-sealable pouches and reels of paper and plastic film construction - Requirements and test methods
本标准对用于包装后面有微生物要求非菌兽药粉剂、可溶性粉剂、散剂、预混剂、颗粒剂、片剂等固体制剂的塑料与铝箔复合膜和复合袋的定义和术语、技术要求、试验方法、检验规则、标志、标签和随行文件、包装、运输和贮存等进行规范。 1）按照本标准条款要求，组织实施了重要试验项目的验证，实施的试验项目有：复合袋
This part of EN 868 provides test methods and values for sealable pouches and reels manufactured from porous materials complying with either EN 868
Packaging for terminally sterilized medical devices - Part 5: Sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods
This document specifies test methods and values for sealable pouches and reels manufactured from porous materials complying with either EN 868 part 2@
Packaging for terminally sterilized medical devices - Part 5: Sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods
Packaging for terminally sterilized medical devices - Part 5 : sealable pouches and reels of porous materials and plastic film construction - Requirements and test methods.
Sealing Cartridge For Two Component Materials
Schv?lení ST SEV 4769 34 dopni uěilu ministeustvo ?kolství ?SR. Zpracovatel: F?ikullíi slrnjní ?eského vysokého u?eni teehnick?ho v Praze, Dne
Representation of seals on nssembly drawings
This notice should be filed in front of, MIL-S-38714B(USAF) dated 15 May 1987
SEALING CARTRIDGE FOR TWO COMPONENT MATERIALS
and similar materials. This specification covers cartridges which are used to store, mix and apply sealants, adhesives
SEALING CARTRIDGE FOR TWO COMPONENT MATERIALS
Packaging materials and systems for medical devices which are to be sterilized Part 5: Heat and self-sealable pouches and reels of paper and plastic film construction Requirements and test methods Incorporating corrigendum October 2001
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