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Delivery: <= 4 days. True-PDF full-copy in English will be manually translated and delivered via email. GB/T 13074-2024: Blood purification terminology Status: Valid GB/T 13074: Historical versions
Basic dataStandard ID: GB/T 13074-2024 (GB/T13074-2024)Description (Translated English): Blood purification terminology Sector / Industry: National Standard (Recommended) Classification of Chinese Standard: C45 Classification of International Standard: 01.040.11 Word Count Estimation: 24,230 Date of Issue: 2024-10-26 Date of Implementation: 2025-11-01 Older Standard (superseded by this standard): GB/T 13074-2009 Issuing agency(ies): State Administration for Market Regulation, China National Standardization Administration GB/T 13074-2024: Blood purification terminology---This is an excerpt. Full copy of true-PDF in English version (including equations, symbols, images, flow-chart, tables, and figures etc.), auto-downloaded/delivered in 9 seconds, can be purchased online: https://www.ChineseStandard.net/PDF.aspx/GBT13074-2024ICS 01.040.11 CCSC45 National Standard of the People's Republic of China Replaces GB/T 13074-2009 Blood purification terminology Released on October 26, 2024 Implementation on November 1, 2025 State Administration for Market Regulation The National Standardization Administration issued Table of ContentsPreface III 1 Scope 1 2 Normative references 1 3 Terms and Definitions 1 3.1 Common terms 1 3.2 Hemodialysis, hemofiltration, hemodiafiltration, and hemoconcentration 4 3.3 Hemoperfusion and plasma exchange 7 3.4 Peritoneal dialysis 8 Appendix A (Informative) Comparison of technical changes between this document and GB/T 13074-2009 9 Reference 13 Index 14 Preface This document is in accordance with the provisions of GB/T 1.1-2020 "Guidelines for standardization work Part 1.Structure and drafting rules for standardization documents" Drafting. This document replaces GB/T 13074-2009 "Blood Purification Terminology". Compared with GB/T 13074-2009, except for the structural adjustment and editing Except for the modification, the main technical changes are shown in Appendix A. Please note that some of the contents of this document may involve patents. The issuing organization of this document does not assume the responsibility for identifying patents. This document is proposed by the State Food and Drug Administration. This document is under the jurisdiction of the National Technical Committee for Standardization of Medical Extracorporeal Circulation Equipment (SAC/TC158). This document was drafted by. Guangdong Medical Device Quality Supervision and Inspection Institute, Guangzhou Kangsheng Biotechnology Co., Ltd., Chongqing Shanwaishan Blood Purification Technology Co., Ltd., Shandong Weigao Blood Purification Products Co., Ltd., Bain Medical Equipment (Guangzhou) Co., Ltd., Jiangxi Sanxin Medical Technology Co., Ltd., B. Braun Aldron (Shanghai) Trading Co., Ltd., and Suzhou Baxter Medical Supplies Co., Ltd. The main drafters of this document are. He Xiaofan, Hu Xianghua, Wu Shaohai, Xie Yan, Huang Minju, Xu Suhua, Shi Zhenwei, Luo Qingfeng, Wang Jing, Yin Lianghong, Liu Jun, Yang Zhenggen, Gao Guangyong, Zou Liang, Liao Lei, Liu Bingrong, Li Xiaoyan, and Meng Qinghai. The previous versions of this document and the documents it replaces are as follows. --- First published as GB/T 13074-1991 in.1991, first revised in.2009; ---This is the second revision. Blood purification terminology 1 Scope This document defines hemodialysis, hemofiltration, hemodiafiltration, hemoconcentration, hemoperfusion and plasma exchange, and peritoneal dialysis. Related terms and definitions. This document applies to hemodialysis, hemofiltration, hemodiafiltration, hemoconcentration, hemoperfusion and plasma exchange, and peritoneal dialysis Related scientific research design, production, maintenance, management, teaching, clinical and other aspects. 2 Normative references This document has no normative references. 3 Terms and Definitions 3.1 Common terms 3.1.1 blood purification Technologies that treat certain diseases by removing harmful substances from the blood, including hemodialysis, hemofiltration, hemodiafiltration, and hemoperfusion. effusion, plasma exchange and peritoneal dialysis, etc. 3.1.2 diffusion The process of solute transport across a semipermeable membrane under the influence of a concentration gradient. 3.1.3 convection The process in which the solute passes through the semipermeable membrane along with the filtrate under the action of pressure gradient or transmembrane pressure. 3.1.4 osmosis The process of solvent moving from low concentration to high concentration through a semipermeable membrane. 3.1.5 reverse osmosis The process of applying external pressure to resist osmosis and reverse flow. 3.1.6 Ultrafiltration; UF The process of removing fluid from the blood across a semipermeable membrane under the action of transmembrane pressure. 3.1.7 Net fluid removal The patient has decreased body fluids. 3.1.8 sieving coefficient The ratio of the concentration of the same solute in the filtrate to that in the blood at the same time point. ......Tips & Frequently Asked Questions:Question 1: How long will the true-PDF of GB/T 13074-2024_English be delivered?Answer: Upon your order, we will start to translate GB/T 13074-2024_English as soon as possible, and keep you informed of the progress. 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Otherwise, follow the normal steps: Add to Cart -- Checkout -- Select your currency to pay.Question 5: Should I purchase the latest version GB/T 13074-2024?Answer: Yes. Unless special scenarios such as technical constraints or academic study, you should always prioritize to purchase the latest version GB/T 13074-2024 even if the enforcement date is in future. Complying with the latest version means that, by default, it also complies with all the earlier versions, technically. |
