YY/T 0456.5-2014.Reagents for hematology analyzer-Part 5: Reticulocyte enumeration reagents. 5.6吸光度值 使用波长范围至少在450 nm-~800 nm.扫措精度优f士+0.5 nm的分光光度计测试样本,

YY/T 0567.1-2013/ISO 13408-1 :2008.Aseptic processing of health care products-Part 1:General requirements. YY/T0567的本部分规定了关于经过无菌加工的医疗保健产品的制造过程的开发、确认和日

YY 0570-2013/IEC 60601-2-46: 1998.Medical electrical equipment-Part 2:Particular requirements for the safety of operating tables. 注:一个安全方面危险的例子是手术台的无意

YY/T 0926-2014.Quantitative analysis of DEHP in PVC medical devices. 4.7.3标准溶液 C:精确量取DEHP标准储备液500 μL至100 mL容量瓶中,用无水乙醇稀释定容(DEHP含量: 10 ug/mL)。 4.7.4标准溶

YY/T 0923-2014.Needleless access ports for fluid lines and blood lines-Test method for microbial ingress. 1范围 YY/T 0923规定了液路.血路无针接口微生物侵入试验的方法。 2规范性引用文

YY/T 0916. 1-2014/ISO 80369-1:2010.Small-bore connectors for liquids and gases in healthcare applications-Part 1:General requirements. 5.4泌尿道应用 预期用于泌尿

YY/T 0681.12-2014.Test methods for sterile medical device package-Part 12:Flex durability of flexible barrier films. YY/T 0681的本部分包括了软性屏障膜抗揉搓性的测定。本试验方

YY/T 1288-2015.Nylon blood filter nets for transfusion equipments for single use. 在放大40倍下观察过滤网,其单丝表面应光洁.无毛刺或起毛现象。 5.3焊接牢固度 注:考虑到产品结构、形状的多样性,无法统-给出试验方法

YY/T 0929.1-2014.Sterilizing grade filters for medical infusion equipments-Part 1: Integrity test for fluid filters. YY/T0929的本部分规定了输液器具用滤膜标称孔径不超过0.22

YY/T 0927-2014.Guidance of determination for di(2-ethylhexyI) phthalate (DEHP) released from PVC medical devices. 1范園 YY/T 0927给出了在模拟实际使用条件下,以聚氣乙烯(PVC

YY/T 0865.1-2011/IEC 62127-1:2007.Ultrasonic-Hydrophone-Part 1: Measurement and characterization of medical ultrasonic fields up to 40 MHz. YY/T 0865的

YY/T 0907-2013/ISO 21649: 2006.Needle-free injectors for medical use- Requirements and test methods. 5.3剂量刻度要求 无针注射器的剂量刻度应按照6.4. 1所述的步骤进行。注射的液体剂量刻度为对于