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YY/T 0681的本部分描述了印墨、印刷上层的覆盖漆或涂层化学接触承受能力的评价程序。可能与包装接触的典型化学物质包括水、乙醇、酸等。对于特殊的化学品，其方法的选择以及测量结果的确定与用户讨论协商确定。本部分所列的各种方法提供了对测量方法和收集信息的建议
Test methods of sterile medical device package.Part 6:Evaluation of chemical resistance of printed inks and coatings on flexible packaging materials
本标准提供了用于确定医疗器械菌屏障系统中材料（或包装材料）的生物相容性试验的指南。 本标准不涉及包装材料的所有安全问题
Guide for biological evaluation of packaging materials for medical devices
本部分描述了对软包装材料上墨迹或涂层牢固性的评价方法。本部分预期用于其表面会粘贴胶带并除时表面破坏的软包装材料
Test methods for sterile medical device package.Part 7:Evaluating inks or coating adhesion to flexible packaging materials using tape
Biological evaluation of medical devices - Chemical characterization of medical device materials within a risk management process
1 Scope This document specifies a framework for the identification , and if necessary, quantification of constituents of a medical
Biological evaluation of medical devices - Chemical characterization of medical device materials within a risk management process
Medical devices. Biological evaluation of medical devices. Part 18. Chemical characterization of materials
Test methods for sterile medical device packaging-part 12: rubbing resistance of soft barrier materials
1.1 This guide provides information to determine the appropriate testing for biocompatibility of medical device packaging materials that have
Standard Guide for Biocompatibility Evaluation of Medical Device Packaging Materials
Biological evaluation of medical devices —Part 18: Chemical characterization of medical device materials within a risk management process
Biological evaluation of medical devices —Part 18: Chemical characterization of medical device materials within a risk management process
Biological evaluation of medical devices Part 18 : Chemical characterization of medical device materials within a risk management process
Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
Évaluation biologique des dispositifs médicaux - Partie 18 : caractérisation chimique des matériaux des dispositifs médicaux au sein d'un processus de gestion du risque
Biological evaluation of medical devices－Part 18：Chemical characterization of materials
Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/DAM 1:2021)
YY/T 0681的本部分描述了印墨、印刷上层的覆盖漆或涂层化学接触承受能力的评价程序。可能与包装接触的典型化学物质包括水、乙醇、酸等。对于特殊的化学品，其方法的选择以及测量结果的确定与用户讨论协商确定。本部分所列的各种方法提供了对测量方法和收集信息的建议
Test methods of sterile medical device package.Part 6:Evaluation of chemical resistance of printed inks and coatings on flexible packaging materials
本标准提供了用于确定医疗器械菌屏障系统中材料（或包装材料）的生物相容性试验的指南。 本标准不涉及包装材料的所有安全问题
Guide for biological evaluation of packaging materials for medical devices
本部分描述了对软包装材料上墨迹或涂层牢固性的评价方法。本部分预期用于其表面会粘贴胶带并除时表面破坏的软包装材料
Test methods for sterile medical device package.Part 7:Evaluating inks or coating adhesion to flexible packaging materials using tape
Biological evaluation of medical devices - Chemical characterization of medical device materials within a risk management process
1 Scope This document specifies a framework for the identification , and if necessary, quantification of constituents of a medical
Biological evaluation of medical devices - Chemical characterization of medical device materials within a risk management process
Medical devices. Biological evaluation of medical devices. Part 18. Chemical characterization of materials
Test methods for sterile medical device packaging-part 12: rubbing resistance of soft barrier materials
1.1 This guide provides information to determine the appropriate testing for biocompatibility of medical device packaging materials that have
Standard Guide for Biocompatibility Evaluation of Medical Device Packaging Materials
Biological evaluation of medical devices —Part 18: Chemical characterization of medical device materials within a risk management process
Biological evaluation of medical devices —Part 18: Chemical characterization of medical device materials within a risk management process
Biological evaluation of medical devices Part 18 : Chemical characterization of medical device materials within a risk management process
Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process (ISO 10993-18:2020)
Évaluation biologique des dispositifs médicaux - Partie 18 : caractérisation chimique des matériaux des dispositifs médicaux au sein d'un processus de gestion du risque
Biological evaluation of medical devices－Part 18：Chemical characterization of materials
Biological evaluation of medical devices - Part 18: Chemical characterization of medical device materials within a risk management process - Amendment 1: Determination of the uncertainty factor (ISO 10993-18:2020/DAM 1:2021)
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