YY/T 1758-2020.Cardiovascular implants- -Pulmonary valve conduit. 1范围 YY/T 1758规定了肺动脉带船管道的基本要求。 YY/T 1758适用于娇正或重建右心室流出道的肺动脉带鲜管道. YY/T 1758不适用于同种异体和自体组

YY/T 1759-2020.Guide for design and evaluation of primary flexible packaging for medical devices. 1范围 YY/T 1759给出了医疗器械软性初包装设计与评价的指南。本标准未涉及可接受准则。注。可接受在

YY/T 1701-2020.Medical grade Ti-6AI-4V/Ti-6AI-4V ELI powder used for additive manufacturing. 1范围 YY/T 1701规定了用于增材制造的医用Ti6A-4V/Ti-6AI-4V ELI粉末的性能要求.试验方

YY/T 0771.2-2020.Medical devices utilizing animal tissues and their derivatives-Part 2 :Controls on sourcing, collection and handling. 1范围 YY/T0771的本部

YY/T 1695-2020.Medical devices for human assisted reproductive technology-Determination of amino acids in human assisted reproductive media. 1范围 YY/T

YY/T 9706.106-2021.Medical electrical equipment-Part 1-6 : General requirements for basic safety and essential performance-Collateral Standard : Usabi

YY/T 1775.1-2021.Biological evaluation of absorbable medical devices-Part 1 :Guidance for absorbable implants. 1范園 YY/T1775的本部分规定了对可吸收植人物进行生物学评价的通用指南,

YY/T 1465.7-2021.Immunogenic evaluation method of medical devices-Part 7:Liquid phase multiplex protein quantification technique by flow cytometry. 1范

YY/T 0616.7-2020.Medical gloves for single use- -Part 7: Test method for the immunological measurement of antigenic protein. 1范围 YY/T0616的本部分规定了一次性使用医

YY 9706.111-2021.Medical elec trical equipment- Part 1-11: General requirements forbasic safety and essential performance- -Collateral Standard : Requ