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现行 UNE-EN 13824:2005
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Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements 医疗器械的灭菌.液体医疗器械的无菌处理.要求
发布日期: 2005-05-25
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发布单位或类别: 西班牙-西班牙标准
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现行
DIN EN 13824
Sterilization of medical devices - Aseptic processing of liquid medical devices - Requirements
医疗器械的灭菌.液体医疗器械的无菌处理.要求;德文版EN 13824:2004
2005-02-01
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BS EN 556-2-2015
Sterilization of medical devices. Requirements for medical devices to be designated "STERILE"-Requirements for aseptically processed medical devices
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UNE-EN 556-2-2004
Sterilization of medical devices - Requirements for medical devices to be designated STERILE - Part 2: Requirements for aseptically processed medical devices
医疗器械的灭菌.指定无菌医疗器械的要求.第2部分:无菌处理医疗器械的要求
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现行
YY/T 0615.2-2007
标示“无菌”医疗器械的要求 第2部分:无菌加工医疗器械的要求
Requirements for medical devices to be designated "STERILE"—Part 2:Requirements for aseptically processed medical devices
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现行
BS EN ISO 14160-2021
Sterilization of health care products. Liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives. Requirements for characterization, development, validation and routine control of a sterilization process for medical devices
医疗保健产品的消毒 利用动物组织及其衍生物的一次性医疗器械用液体化学杀菌剂 医疗器械灭菌过程的特征描述、开发、验证和常规控制要求
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现行
AAMI/ISO 14160-2011/(R)2016
Sterilization of health care products - liquid chemical sterilizing agents for single-use medical devices utilizing animal tissues and their derivatives - requirements for characterization, development, validation and routine control of a sterilization process for medical devices
医疗保健产品的灭菌.利用动物组织及其衍生物的一次性医疗器械用液体化学灭菌剂.医疗器械灭菌过程的特性、开发、验证和常规控制要求
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一次性医疗器械的灭菌 包含动物产地的材料 - 液体化学杀菌剂的灭菌验证和常规控制
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