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YY 0054-2023   Haemodialysis equipment (English Version)
Standard No.: YY 0054-2023 Status:to be valid remind me the status change

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Word Count: 12000 words Translation Price(USD):360.0 remind me the price change

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Implemented on:2026-1-15 Delivery: via email in 1 business day

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,,2026-1-15,49E5150FAE49C4F21673940191534
Standard No.: YY 0054-2023
English Name: Haemodialysis equipment
Chinese Name: 血液透析设备
Professional Classification: YY    Professional Standard - Pharmaceutics
Source Content Issued by: State Drug Administration
Issued on: 2023-01-13
Implemented on: 2026-1-15
Status: to be valid
Superseding:YY 0054-2010 Haemodialysis equipment
Target Language: English
File Format: PDF
Word Count: 12000 words
Translation Price(USD): 360.0
Delivery: via email in 1 business day
Haemodialysis equipment 1 Scope This document specifies the classification and requirements of haemodialysis equipment and describes the test methods. This document is applicable to haemodialysis equipment with automatical preparation of dialysis fluid (hereinafter referred to as equipment). This document is not applicable to: ——haemodialysis water treatment equipment; ——peritoneal dialysis equipment; ——hemoperfusion, plasma substitution and plasma adsorption equipment; ——continuous blood purification equipment; ——central delivery system; ——haemodialysis equipment with renewable dialysis fluid. 2 Normative references The following documents contain provisions which, through reference in this text, constitute provisions of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. GB 9706.1 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance GB 9706.216 Medical electrical equipment - Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment GB/T 14710 Environmental requirement and test methods for medical electrical equipment YY 0598 Concentrates for haemodialysis and related therapies YY 1272-2016 Dialysis fluid filter YY 9706.108 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 3 Terms and definitions For the purposes of this document, the terms and definitions given in GB 9706.216 and the following apply. 3.1 A0 value time equivalent to the time measured in seconds during thermal disinfection at 80℃, calculated using Equation (1): A0=∑10[(T-80)/z]×Δt (1) where, A0——the value of A when z is 10℃; T——the thermal disinfection maintenance temperature, ℃; Δt——the selected time interval, specified by the manufacturer, s. 3.2 automatical preparation of dialysis fluid process of preparing dialysis fluid that meets the clinical requirements, during which the ratio of haemodialysis concentrate to dialysis water is automatically controlled by equipment 3.3 online equipment equipment capable of online hemofiltration therapy (online HF therapy) and/or online haemodiafiltration therapy (online HDF) 4 Classification Equipment may be classified into haemodialysis type and haemodiafiltration type. 5 Requirements 5.1 Normal operating conditions of equipment The following conditions shall be met for the normal operation of the equipment: a) ambient temperature: 10~30℃ or as specified by the manufacturer;
Foreword i 1 Scope 2 Normative references 3 Terms and definitions 4 Classification 5 Requirements 5.1 Normal operating conditions of equipment 5.2 Flow rate control 5.3 Dialysis fluid composition 5.4 Filtration-sterilization system 5.5 Dialysis fluid conductivity control and protection 5.6 Temperature control 5.7 Pressure monitoring 5.8 Flow rate, temperature and conductivity stability of dialysis fluid 5.9 Blood leak protective system 5.10 Prevention against air admission 5.11 pH measuring device 5.12 Grid power supply interruption 5.13 Degassing function 5.14 Liquid waste protection 5.15 Disinfection 5.16 Operating noise 5.17 Appearance and structure 5.18 Safety requirements 5.19 Environmental test 6 Test methods 6.1 Test conditions 6.2 Flow rate control test 6.3 Dialysis fluid composition test 6.4 Filtration-sterilization system test 6.5 Dialysis fluid conductivity control and protection test 6.6 Temperature control system test 6.7 Pressure monitoring test 6.8 Test of flow rate, temperature and conductivity stability of dialysis fluid 6.9 Blood leak protective system test 6.10 Prevention against air admission 6.11 pH measuring device test 6.12 Grid power supply interruption test 6.13 Degassing function test 6.14 Liquid waste protection test 6.15 Disinfection test 6.16 Operating noise test 6.17 Appearance and structure test 6.18 Test for safety requirements 6.19 Environmental test
Referred in YY 0054-2023:
*GB 9706.1-2020 Medical electrical equipment—Part 1: General requirements for basic safety and essential performance
*GB 9706.216-2021 Medical electrical equipment—Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
*GB/T 14710-2009 Environmental requirement and test methods for medical electrical equipment
*YY 0598-2015/XG2-2018 Concentrates for hemodialysis and related therapies
*YY 1272-2016 Dialysis fluid filter
*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
Code of China
Standard
YY 0054-2023  Haemodialysis equipment (English Version)
Standard No.YY 0054-2023
Statusto be valid
LanguageEnglish
File FormatPDF
Word Count12000 words
Price(USD)360.0
Implemented on2026-1-15
Deliveryvia email in 1 business day
Detail of YY 0054-2023
Standard No.
YY 0054-2023
English Name
Haemodialysis equipment
Chinese Name
血液透析设备
Chinese Classification
Professional Classification
YY
ICS Classification
Issued by
State Drug Administration
Issued on
2023-01-13
Implemented on
2026-1-15
Status
to be valid
Superseded by
Superseded on
Abolished on
Superseding
YY 0054-2010 Haemodialysis equipment
Language
English
File Format
PDF
Word Count
12000 words
Price(USD)
360.0
Keywords
YY 0054-2023, YY/T 0054-2023, YYT 0054-2023, YY0054-2023, YY 0054, YY0054, YY/T0054-2023, YY/T 0054, YY/T0054, YYT0054-2023, YYT 0054, YYT0054
Introduction of YY 0054-2023
Haemodialysis equipment 1 Scope This document specifies the classification and requirements of haemodialysis equipment and describes the test methods. This document is applicable to haemodialysis equipment with automatical preparation of dialysis fluid (hereinafter referred to as equipment). This document is not applicable to: ——haemodialysis water treatment equipment; ——peritoneal dialysis equipment; ——hemoperfusion, plasma substitution and plasma adsorption equipment; ——continuous blood purification equipment; ——central delivery system; ——haemodialysis equipment with renewable dialysis fluid. 2 Normative references The following documents contain provisions which, through reference in this text, constitute provisions of this document. For dated references, only the edition cited applies. For undated references, the latest edition of the referenced document (including any amendments) applies. GB 9706.1 Medical electrical equipment - Part 1: General requirements for basic safety and essential performance GB 9706.216 Medical electrical equipment - Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment GB/T 14710 Environmental requirement and test methods for medical electrical equipment YY 0598 Concentrates for haemodialysis and related therapies YY 1272-2016 Dialysis fluid filter YY 9706.108 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 3 Terms and definitions For the purposes of this document, the terms and definitions given in GB 9706.216 and the following apply. 3.1 A0 value time equivalent to the time measured in seconds during thermal disinfection at 80℃, calculated using Equation (1): A0=∑10[(T-80)/z]×Δt (1) where, A0——the value of A when z is 10℃; T——the thermal disinfection maintenance temperature, ℃; Δt——the selected time interval, specified by the manufacturer, s. 3.2 automatical preparation of dialysis fluid process of preparing dialysis fluid that meets the clinical requirements, during which the ratio of haemodialysis concentrate to dialysis water is automatically controlled by equipment 3.3 online equipment equipment capable of online hemofiltration therapy (online HF therapy) and/or online haemodiafiltration therapy (online HDF) 4 Classification Equipment may be classified into haemodialysis type and haemodiafiltration type. 5 Requirements 5.1 Normal operating conditions of equipment The following conditions shall be met for the normal operation of the equipment: a) ambient temperature: 10~30℃ or as specified by the manufacturer;
Contents of YY 0054-2023
Foreword i 1 Scope 2 Normative references 3 Terms and definitions 4 Classification 5 Requirements 5.1 Normal operating conditions of equipment 5.2 Flow rate control 5.3 Dialysis fluid composition 5.4 Filtration-sterilization system 5.5 Dialysis fluid conductivity control and protection 5.6 Temperature control 5.7 Pressure monitoring 5.8 Flow rate, temperature and conductivity stability of dialysis fluid 5.9 Blood leak protective system 5.10 Prevention against air admission 5.11 pH measuring device 5.12 Grid power supply interruption 5.13 Degassing function 5.14 Liquid waste protection 5.15 Disinfection 5.16 Operating noise 5.17 Appearance and structure 5.18 Safety requirements 5.19 Environmental test 6 Test methods 6.1 Test conditions 6.2 Flow rate control test 6.3 Dialysis fluid composition test 6.4 Filtration-sterilization system test 6.5 Dialysis fluid conductivity control and protection test 6.6 Temperature control system test 6.7 Pressure monitoring test 6.8 Test of flow rate, temperature and conductivity stability of dialysis fluid 6.9 Blood leak protective system test 6.10 Prevention against air admission 6.11 pH measuring device test 6.12 Grid power supply interruption test 6.13 Degassing function test 6.14 Liquid waste protection test 6.15 Disinfection test 6.16 Operating noise test 6.17 Appearance and structure test 6.18 Test for safety requirements 6.19 Environmental test
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Keywords:
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