GB 12264-1990
Replaced
YY/T 0793.1-2022
Active
Industry standards-Medicine
YY/T 0793.1-2022 Preparation and quality management of fluids for haemodialysis and related therapies—Part 1:Water treatment equipment for haemodialysis applications and related therapies
YY/T 0793.1-2022 Preparation and quality management of fluids for haemodialysis and related therapies—Part 1:Water treatment equipment for haemodialysis applications and related therapies
Basic Information
Standard Code:
YY/T 0793.1-2022
Standard Type:
Industry standards
Standard Status:
Active
is_force_gb:
no
CCS Name:
Extracorporeal circulation, artificial organs, and prosthetic devices
ICS Name:
Surgical implants, prostheses, and orthoses
Publish Date:
2022-07-01
Implement Date:
2024-07-01
Publisher:
国家药品监督管理局
Technical Committee:
全国医用体外循环设备标准化技术委员会(SAC/TC 158)
Pages:
28 pages
Scope
本文件规定了血液透析和相关治疗用水处理设备的术语和定义、要求、试验方法和标记。
本文件适用于对生活饮用水进行处理以传输到血液透析和相关治疗中使用的装置,水的使用包括:
a) 在透析设施中将粉末或其他高度浓缩的介质制备成浓缩液;
b) 制备透析液,包括可用于制备置换液的透析液;
c) 对于可多次使用的透析器预期用于单次使用后的再处理;
d) 对未明确标示预期用于单次使用的透析器的再处理。
本文件适用于从生活饮用水进入水处理系统的输送点到透析用水使用点之间的所有装置、管路及配件,例如水净化装置、在线水质监测器(例如电导率监测器)和用于分配透析用水的管路系统。
本文件不适用于:透析液供液系统(按比例分配水和浓缩液生产透析液)、吸附器透析液再生系统(再生并再循环少量透析液、透析浓缩液)、血液透析滤过系统、血液滤过系统、用于处理可多次使用透析器的系统及腹膜透析系统。其中一些装置,如透析液分配系统和浓缩液,在其他文件中有所说明,例如YY 0598和YY/T 0793.4。
本文件也不适用于ISO 23500-1所述对用于透析液、浓缩液制备或透析器再处理的水纯度的持续监测。
Development Information
Drafting Units:
广东省医疗器械质量监督检验所、贝朗爱敦(上海)贸易有限公司、苏州百特医疗用品有限公司、费森尤斯医药研发(上海)有限公司
Drafting Persons:
吴少海、梁泽鑫、王闯、蔡海青、温少君、颜林、柯军、何晓帆、李晓艳、张远杰、王珊珊
Same series standard
Replace the following standards
YY 0793.1-2010 Technical requirements of water treatment equipments for haemodialysis applications and related therapies—Part 1:For multi-beds haemodialysis
YY 0793.2-2011 Technical requirements of water treatment equipments for haemodialysis applications and related therapies—Part 2:For single-bed haemodialysis
Referenced Standards
YY 9706.108-2021 Medical electrical equipment—Part 1-8:General requirements for basic safety and essential performance-Collateral standard:General requirements,tests and guidance for alarm systems in medical electrical equipment and medical electrical systems
ISO 23500-1:2019
GB 9706.1-1995 Medical electrical equipment—Part 1:General requirements for safety
GB 9706.1-2007 Medical electrical equipment—Part 1:General requirements for safety
GB 9706.1-2020 Medical electrical equipment—Part 1:General requirements for basic safety and essential performance
GB/T 14710-1993 The environmental requirements and test methods for medical electrical equipment
GB/T 14710-2009 Environmental requirement and test methods for medical electrical equipment
YY 0572-2005 Water for haemodialysis and related therapies
YY 0572-2015 Water for haemodialysis and related therapies
Adopt standards
ISO 23500-2:2019
Related Standards
GB 12279-1990
Replaced
GB 12279-1990 Cardiac valve prostheses general technical specification
GB 12417-1990
Replaced
GB 12417-1990 The general technological conditions of surgical metal implant
GB/T 13461-1992
Replaced
GB/T 13461-1992 Synthetic resin blow knee prostheses
GB/T 14191-1993
Replaced
GB/T 14191-1993 Terminology for prosthetics and orthotics
GB 14722-1993
Replaced