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blood

blood, Total:498 items.

In the international standard classification, blood involves: Medical equipment, Meat, meat products and other animal produce, Laboratory medicine, Sacks. Bags, Hospital equipment, Refrigerating technology, Shop fittings, Precision mechanics, Vocabularies, Medical sciences and health care facilities in general, Protective equipment, Pharmaceutics, First aid, Education, Veterinary medicine, Food products in general, Protection against crime, Character sets and information coding, Biology. Botany. Zoology, Quality, Radiation measurements, Information technology (IT) in general, Plastics, Graphical symbols, Thermodynamics and temperature measurements, Farming and forestry.

ES-AENOR, blood

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, blood

GB/T 13074-1991 Terms of blood purification--Hemodialysis and hemofiltration
GB/T 21278-2007 Refrigerators for conserved blood
GB/T 13074-2009 Terms of blood purification
GB 9706.2-2003 Medical electrical equipment--Part 2-16: Particular requirements for the safety of haemodialysis,haemodiafiltration and haemofiltration equipment
GB 14232.1-2004 Plastics collapsible containers for human blood and blood components-Part 1:Conventional containers
GB/T 14232.1-2020 Plastics collapsible containers for human blood and blood components—Part 1:Conventional containers
GB 14232.3-2011 Plastics collapsible containers for human blood and blood components. Part 3:Blood bag systems with integrated features
GB 15593-1995 Plasticized polyvinyl chloride (PVC) compounds for transfusion (infusion) equipment
GB/T 14232.2-2015 Bag plastic containers for human blood and blood components - Part 2: Graphical symbols for labeling and instructions for use

Taiwan Provincial Standard of the People's Republic of China, blood

CNS 14193-1998 Haemodialysers,hasmofilters and haemoconcentrators
CNS 14194-1998 Extracorporeal blood circuit for haemodialysers hasmofilters and haemoconcentrators
CNS 15036-1-2006 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers

Korean Agency for Technology and Standards (KATS), blood

KS P ISO 8638:2012 Cardiovascular implants and extracorporeal systems －Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
KS P 4907-2013 Haemodialysers, haemofilters and haemoconcentrators
KS P ISO 8637:2012 Cardiovascular implants and extracorporeal systems－Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
KS P ISO 8638-2012(2017) Cardiovascular implants and extracorporeal systems －Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
KS P 4907-2011 Haemodialysers, haemofilters and haemoconcentrators
KS C IEC 60601-2-16:2002 Haemodialysis, haemodiafiltration and haemofiltration equipment
KS P ISO 3826-4:2019 Plastics collapsible containers for human blood and blood components — Part 4: Aphaeresis blood bag systems with integrated features
KS K ISO 16603:2012 Clothing for protection against contact with blood and body fluids-Determination of the resistance of protective clothing materials to penetration by blood and body fluids-Test method using synthetic blood
KS C IEC 60601-2-16:2018 Medical electrical equipment — Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
KS P ISO 3826-1:2021 Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers
KS P ISO 8637:2018 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
KS K ISO 16603-2012(2017) Clothing for protection against contact with blood and body fluids－Determination of the resistance of protective clothing materials to penetration by blood and body fluids－Test method using synthetic
KS P ISO 13959:2009 Water for haemodialysis and related therapies
KS P ISO 13959-2009(2019) Water for haemodialysis and related therapies
KS P ISO 13958:2009 Concentrates for haemodialysis and related therapies
KS P ISO 13958-2009(2019) Concentrates for haemodialysis and related therapies
KS P 6108-2010(2021) Blood and pharmacy storage electric refrigerator and freezers
KS P ISO 23500-3:2021 Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies

International Organization for Standardization (ISO), blood

ISO 8638:1989 Extracorporeal blood circuit for haemodialysers, haemofilters and haemoconcentrators
ISO 8637:1989 Haemodialysers, haemofilters and haemoconcentrators
ISO/FDIS 8637-2:2023 Extracorporeal systems for blood purification — Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
ISO/DIS 8637-1 Extracorporeal systems for blood purification — Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
ISO/CD 8637-1 Extracorporeal systems for blood purification — Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
ISO 8637-1:2017 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
ISO/DIS 8637-2 Extracorporeal systems for blood purification — Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
ISO 8637:2004 Cardiovascular implants and artificial organs - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
ISO 8637:2010 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
ISO 8638:2004 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
ISO 8638:2010 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
ISO 3826:1993 Plastics collapsible containers for human blood and blood components
ISO 16603:2004 Clothing for protection against contact with blood and body fluids - Determination of the resistance of protective clothing materials to penetration by blood and body fluids - Test method using synthetic blood
ISO 3826-1:2003 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers
ISO 3826-1:2013 Plastics collapsible containers for human blood and blood components.Part 1: Conventional containers
ISO 8637:2010/Amd 1:2013 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators - Amendment 1: Revision to Figure 2 - Main fitting dimensions of dialysis fluid inlet and outlet ports
ISO 3826-1:2019/Amd 1:2023 Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers — Amendment 1
ISO 13959:2009 Water for haemodialysis and related therapies
ISO 13959:2002 Water for haemodialysis and related therapies
ISO 13959:2014 Water for haemodialysis and related therapies
ISO 3826-3:2006 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features
ISO 13958:2014 Concentrates for haemodialysis and related therapies
ISO 3826-4:2015 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features
ISO 13958:2002 Concentrates for haemodialysis and related therapies
ISO/ASTM 51939:2002 Practice for blood irradiation dosimetry
ISO/ASTM 51939:2005 Practice for blood irradiation dosimetry
ISO/ASTM 51939:2013 Practice for blood irradiation dosimetry
ISO/ASTM 51939:2017 Practice for blood irradiation dosimetry
ISO 13958:2009 Concentrates for haemodialysis and related therapies
ISO/DIS 23500-3 Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies
ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies
ISO/DIS 23500-4 Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapies

Japanese Industrial Standards Committee (JISC), blood

JIS T 3250:2022 Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
JIS T 3250:2005 Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
JIS T 3250:2011 Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
JIS T 3250:2013 Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
JIS T 3232:2005 Blood filters for cardiopulmonary bypass systems
JIS T 3217:2011 Plastic collapsible containers for human blood and blood components
JIS T 3217:2016 Plastic collapsible containers for human blood and blood components
JIS T 3217:2005 Plastic collapsible containers for human blood and blood components
JIS T 3248:2022 Extracorporeal blood circuit
JIS T 3248:2005 Extracorporeal blood circuit
JIS T 3248:2011 Extracorporeal blood circuit
JIS T 3248:2012 Extracorporeal blood circuit
JIS T 3232:2011 Blood filters for cardiopulmonary bypass systems
JIS T 3232:2016 Blood filters for cardiopulmonary bypass systems
JIS T 8060:2007 Clothing for protection against contact with blood and body fluids -- Determination of the resistance of protective clothing materials to penetration by blood and body fluids -- Test method using synthetic blood
JIS T 8060:2015 Clothing for protection against contact with blood and body fluids -- Determination of the resistance of protective clothing materials to penetration by blood and body fluids -- Test method using synthetic blood
JIS T 0601-2-16:2008 Medical electrical equipment -- Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemodiafiltration equipment
JIS T 0601-2-16:2022 Medical electrical equipment -- Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
JIS T 1603:1995 Electric motor driven blood pump for cardiopulmonary bypass
JIS T 0601-2-16:2014 Medical electrical equipment -- Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment

European Committee for Standardization (CEN), blood

EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637:2010, including Amendment 1 2013-04-01)
EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
EN 1283:1996 Haemodialysers, Haemodiafilters, Haemofilters, Haemoconcentrators and Their Extracorporeal Circuits
prEN ISO 8637-2 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO/DIS 8637-2:2022)
EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers@ haemodiafilters and haemofilters
EN 12022:1999 Blood Gas Exchangers
EN ISO 3826-1:2019 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2019)
EN ISO 3826-1:2013 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers
EN ISO 3826-1:2003 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers ISO 3826-1:2003
EN ISO 3826-3:2007 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated
EN ISO 3826-1:2019/A1:2023 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers - Amendment 1 (ISO 3826-1:2019/Amd1:2023)

Professional Standard - Medicine, blood

YY 0053-2016 Hemodialysis and related treatments Hemodialyzers, hemodiafilters, hemofilters and hemoconcentrators
YY 0054-2003 Haemodialysis、haemodiafiltration and haemofiltration equipment
YY 0053-2008 Cardiovascular implants and artificial organs.Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
YY/T 1460-2016 Blood rheometer
YY/T 0653-2008 Hematology analyzer
YY/T 0653-2017 Hematology analyzer
YY/T 0168-2007 Blood refrigerator
YY/T 0848-2011 Blood irradiator
YY 0168-1994 blood cooler
YY 0054-2010 Haemodialysis equipment
YY 0790-2010 Hemoperfusion equipment
YY/T 1545-2017 Evaluation of concentrates for hemodialysis in connection with hemodialysis equipment
YY 0267-2016 Extracorporeal circulation blood circuit of blood purification device for hemodialysis and related treatment
YY 0645-2008 Continuous blood purification equipment
YY/T 0700-2008 Clothing for protection against contact with blood and body fluids.Determination of the resistance of protective clothing materials to penetration by blood and body fluids.Test method using synthetic blood
YY 0464-2019 Single use hemoperfutor
YY 0464-2003 Single use hemoperfutor
YY 0464-2009 Disposable hemoperfutor
YY/T 1273-2016 Roller pump for auxiliary blood purification
YY 1273-2016 Roller pump for auxiliary blood purification
YY/T 1920-2023 Dialyzer hemocompatibility test
YY 0572-2015 Water for haemodialysis and related therapies
YY 0572-2005 Water for haemodialysis and related therapies
YY 1413-2016 Centrifugal blood component separation equipment
YY 0267-1995 Extracorporeal blood circuit for blood purification devices
YY/T 1452-2016 Dry hematology analyzer (centrifuge method)
YY 0765.1-2009 Sets for inactivation of viruses in blood and blood components for single use.Part 1:Sets for virus photodynamic inactivation with methylene blue
YY 0598-2015(A1) Concentrates for haemodialysis and related therapies
YY 0598-2006 Concentrates for heamodialysis and related therapies
YY/T 0598-2015 Concentrates for haemodialysis and related therapies
YY 0598-2015 Concentrates for haemodialysis and related therapies
YY/T 0456.2-2014 Reagents for hematology analyzer.Part 2:Hemolysin
YY/T 0456.1-2014 Reagents for hematology analyzer.Part 1:Rinse
YY 0327-2002 Human blood containers for UV rays transmission therapy for single use

British Standards Institution (BSI), blood

BS EN ISO 8637-1:2020 Extracorporeal systems for blood purification. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
BS EN 1283:1996 Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
23/30470631 DC BS ISO 8637-1. Extracorporeal systems for blood purification - Part 1. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
22/30456450 DC BS EN ISO 8637-2. Extracorporeal systems for blood purification - Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
BS EN ISO 8637-2:2018 Tracked Changes. Extracorporeal systems for blood purification. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
16/30331650 DC BS EN ISO 8637-1. Extracorporeal systems for blood purification. Part 1. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
BS EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
12/30254337 DC BS ISO 8637 AMD1. Cardiovascular implants and extracorporeal systems. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
BS EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
BS EN 12022:1999 Blood-gas exchangers
BS EN ISO 3826-1:2013 Plastics collapsible containers for human blood and blood components. Conventional containers
BS EN 60601-2-16:2015 Medical electrical equipment. Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
BS ISO 16603:2004 Clothing for protection against contact with blood and body fluids - Determination of the resistance of protective clothing materials to penetration by blood and body fluids - Test method using synthetic blood
BS EN ISO 3826-1:2019+A1:2023 Plastics collapsible containers for human blood and blood components - Conventional containers
BS 4376:1982 Specification for electrically operated blood storage refrigerators
BS EN 60601-2-16:1998 Medical electrical equipment. Particular requirements for safety. Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment
BS EN IEC 60601-2-16:2019 Tracked Changes. Medical electrical equipment. Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
BS EN ISO 3826-3:2007 Plastics collapsible containers for human blood and blood components - Blood bag systems with integrated features
BS EN ISO 3826-3:2006 Plastics collapsible containers for human blood and blood components. Blood bag systems with integrated features
BS ISO 3826-3:2006 Plastics collapsible containers for human blood and blood components - Blood bag systems with integrated features
BS EN ISO 3826-4:2015 Plastics collapsible containers for human blood and blood components. Aphaeresis blood bag systems with integrated features
BS ISO 13959:2014 Water for haemodialysis and related therapies
BS ISO 13959:2009 Water for haemodialysis and related therapies
21/30433073 DC BS EN IEC 60601-2-16. Medical electrical equipment. Part 2-16. Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
BS EN ISO 3826-2:2008 Plastics collapsible containers for human blood and blood components - Part 2: Graphical symbols for use on labels and instruction leaflets
BS EN 13867:2002+A1:2009 Concentrates for haemodialysis and related therapies
BS EN 13867:2002 Concentrates for haemodialysis and related therapies
BS EN ISO 13958:2015 Concentrates for haemodialysis and related therapies

RU-GOST R, blood

GOST 33674-2015 Blood and processed products. Specifications
GOST R 53470-2009 Blood and blood components. Management on application of components of donor blood
GOST ISO 8638-2012 Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemoconcentrators. Technical requirements and test methods
GOST R 52938-2008 Blood and blood components. Containers with blood or blood components. Labeling
GOST ISO 8637-2012 Haemodialysers, haemofiltres and haemoconcentrators. Technical requirements and test methods
GOST R ISO 8638-1999 Extracorporeal blood circuit for haemodialysers, haemofilters and haemoconcentrators. Technical requirements and test methods
GOST R ISO 8637-1999 Haemodialysers, haemofilters and haemoconcentrators. Technical requirements and test methods
GOST R 50267.16-2003 Medical electrical equipment. Part 2. Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment
GOST R 50267.16-1993 Medical electrical equipment. Part 2. Particular requirements for safety of haemodialysis equipment
GOST R 52556-2006 Water for hemodialysis. Specifications
GOST R 53420-2009 Blood and blood components. General requirements for quality assurance of collection, processing and use of blood and blood components
GOST R IEC 60601-2-16-2016 Medical electrical equipment. Part 2-16. Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration
GOST R ISO 13958-2015 Concentrates for haemodialysis and related therapies
GOST 4.317-1985 System of product-quality indices. Systems and sets for blood administration. Nomenclature of indices
GOST 27422-1987 Apparatus for nonkidney blood treatment. General specifications

US-FCR, blood

FCR 21 CFR PART 630-2015 GENERAL REQUIREMENTS FOR BLOOD, BLOOD COMPONENTS, AND BLOOD DERIVATIVES
FCR 21 CFR PART 630-2013 GENERAL REQUIREMENTS FOR BLOOD, BLOOD COMPONENTS, AND BLOOD DERIVATIVES
FCR 21 CFR PART 640-2015 ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS
FCR 21 CFR PART 640-2014 ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS
FCR 21 CFR PART 640-2013 ADDITIONAL STANDARDS FOR HUMAN BLOOD AND BLOOD PRODUCTS
FCR 21 CFR PART 606-2015 CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
FCR 21 CFR PART 606-2013 CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
FCR 21 CFR PART 606-2014 CURRENT GOOD MANUFACTURING PRACTICE FOR BLOOD AND BLOOD COMPONENTS
FCR 21 CFR PART 607-2015 ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS
FCR 21 CFR PART 607-2014 ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS
FCR 21 CFR PART 607-2013 ESTABLISHMENT REGISTRATION AND PRODUCT LISTING FOR MANUFACTURERS OF HUMAN BLOOD AND BLOOD PRODUCTS
FCR 21 CFR PART 864-2015 HEMATOLOGY AND PATHOLOGY DEVICES
FCR 21 CFR PART 864-2013 HEMATOLOGY AND PATHOLOGY DEVICES
FCR 21 CFR PART 864-2014 HEMATOLOGY AND PATHOLOGY DEVICES

IN-BIS, blood

IS 13878-1993 Extracorporeal blood circuit for haemodialysers, haemofilters and haemoconcentrators - specification
IS 13890-1994 Haemodialysers, haemofilters and haemoconcentrators - specification

CZ-CSN, blood

CSN ISO 8637:1994 Haemodialysers, haemofilters and haemoconcentrators
CSN 70 3351-1979 Bottles for blood and transfusion and infusion preparations
CSN 70 5225-1965 Blood sedimentation pipette, straight
CSN 70 5220-1962 Glass for haematologic purposes

Danish Standards Foundation, blood

DS/EN ISO 8637-1:2021 Extracorporeal systems for blood purification – Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
DS/EN 1283:1997 Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
DS/ISO 16603:2005 Clothing for protection against contact with blood and body fluids - Determination of the resistance of protective clothing materials to penetration by blood and body fluids - Test method using synthetic blood
DS/EN 60601-2-16/Corr.:2000 Medical electrical equipment - Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment
DS/EN 60601-2-16:1999 Medical electrical equipment - Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment
DS/EN ISO 3826-1:2013 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers
DS/EN ISO 3826-3:2008 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features

Association Francaise de Normalisation, blood

NF EN ISO 8637-1:2020 Systèmes extracorporels pour la purification du sang - Partie 1 : hémodialyseurs, hémodiafiltres, hémofiltres et hémoconcentrateurs
NF EN ISO 8637-2:2018 Systèmes extracorporels pour la purification du sang - Partie 2 : circuit sanguin extracorporel pour les hémodialyseurs, les hémodiafiltres et les hémofiltres
NF S93-302-1*NF EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1 : haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
NF S93-302-2*NF EN ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2 : extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
NF S93-302*NF EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
NF S93-230-3*NF EN ISO 3826-3:2008 Plastics collapsible containers for human blood and blood components - Part 3 : blood bag systems with integrated features
NF S93-303:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
NF EN ISO 3826-1:2019 Poches en plastique souple pour le sang et les composants du sang - Partie 1 : poches conventionnelles
NF C74-322:2002 Medical electrical equipment - Part 2-16 : particular requirement for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment.
NF S93-230-4*NF EN ISO 3826-4:2015 Plastics collapsible containers for human blood and blood components - Part 4 : aphaeresis blood bag systems with integrated features
NF S93-230-1:2013 Plastics collapsible containers for human blood and blood components - Part 1: conventional containers
NF C74-322*NF EN 60601-2-16:2015 Medical electrical equipment - Part 2-16 : particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
NF C74-322*NF EN IEC 60601-2-16:2019 Medical electrical equipment - Part 2-16 : particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
NF EN IEC 60601-2-16:2019 Appareils électromédicaux - Partie 2-16 : exigences particulières pour la sécurité de base et les performances essentielles des appareils d'hémodialyse, d'hémodiafiltration et d'hémofiltration
NF EN ISO 3826-1/A1:2023 Poches en plastique souple pour le sang et les composants du sang - Partie 1 : poches conventionnelles - Amendement 1
NF EN ISO 3826-3:2008 Poches en plastique souple pour le sang et les composants du sang - Partie 3 : systèmes de poches pour le sang avec accessoires intégrés
NF EN ISO 3826-4:2015 Poches en plastique souple pour le sang et les composants du sang - Partie 4 : systèmes de poches d'aphérèse pour le sang avec accessoires intégrés
NF EN ISO 23500-4:2019 Préparation et management de la qualité des liquides d'hémodialyse et de thérapies annexes - Partie 4 : concentrés pour hémodialyse et thérapies apparentées
NF S93-315:2008 Fluids for hemodialysis - Requirements and user recommendations
NF S93-301/IN1:2009 Concentrates for haemodialysis and related therapies.
NF S93-301:2009 Concentrates for haemodialysis and related therapies.
NF S93-305-3*NF EN ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3 : water for haemodialysis and related therapies
NF EN ISO 23500-3:2019 Préparation et management de la qualité des liquides d'hémodialyse et de thérapies annexes - Partie 3 : eau pour hémodialyse et thérapies apparentées
NF EN ISO 3826-2:2008 Poches en plastique souple pour le sang et les composants du sang - Partie 2 : symboles graphiques à utiliser sur les étiquettes et les notices d'utilisation

German Institute for Standardization, blood

DIN EN ISO 8637-1:2020-10 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017); German version EN ISO 8637-1:2020
DIN EN ISO 8637-2:2018-12 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8637-2:2018); German version EN ISO 8637-2:2018 / Note: To be replaced by DIN EN ISO 8637-2 (2023-01).
DIN EN ISO 8637-2:2023-01 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO/DIS 8637-2:2022); German and English version prEN ISO 8637-2:2022 / Note: Date...
DIN EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
DIN 58934-1:1997 Haematology - Control material for the CBC - Part 1: Control bloods
DIN 58934-1:1997-12 Haematology - Control material for the CBC - Part 1: Control bloods
DIN 58931:1995 Haematology - Determination of haemoglobin concentration in blood - Reference method
DIN 58931:2021 Haematology - Determination of haemoglobin concentration in blood - Reference method; Text in German and English
DIN 58931:2021-09 Haematology - Determination of haemoglobin concentration in blood - Reference method; Text in German and English
DIN EN ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8637-2:2018); German version EN ISO 8637-2:2018
DIN 58932-1:2023-08 Haematology - Determination of the concentration of blood corpuscles in blood - Part 1: Blood collection, sample preparation, influence quantities, interference factors; Text in German and English
DIN 58903:2020 Haemostaseology - Deficient plasma - Requirements, preparation; Text in German and English
DIN 58903:2020-04 Haemostaseology - Deficient plasma - Requirements, preparation; Text in German and English
DIN EN 12022:1999 Blood gas exchangers; German version EN 12022:1999
DIN EN 60601-2-16:1999 Medical electrical equipment - Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment (IEC 60601-2-16:1998); German version EN 60601-2-16:1998
DIN 58935-1:1997 Haematologie - Determination of the erythrocyte sedimentation rate in blood - Part 1: Selected method
DIN EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637:2010, including Amendment 1:2013-04-01); German version EN ISO 8637:2014
DIN 58931:2010 Haematology - Determination of haemoglobin concentration in blood - Reference method; Text in German and English
DIN 58932-3:1994 Haematology; determination of the concentration of blood corpuscles in blood; determination of the concentration of erythrocytes; reference method
DIN 58932-4:2003 Haematology - Determination of the concentration of blood corpuscles in blood - Part 4: Reference procedure for the determination of the concentration of leucocytes
DIN 12750:1969 Blood dilution pipettes for blood corpuscles counting
DIN EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8638:2010); German version EN ISO 8638:2014
DIN 58905-1:2016-12 Haemostaseology - Blood collection - Part 1: Preparation of plasma from citrated venous blood for coagulation testing; Text in German and English
DIN 58932-5:2007-10 Haematology - Determination of the concentration of blood corpuscles in blood - Part 5: Reference method for the determination of the concentration of thrombocytes; Text in German and English
DIN 58932-3:2017-01 Haematology - Determination of the concentration of blood corpuscles in blood - Part 3: Reference method for the determination of the concentration of erythrozytes; Text in German and English
DIN 58932-5:2007 Haematology - Determination of the concentration of blood corpuscles in blood - Part 5: Reference method for the determination of the concentration of thrombocytes; Text in German and English
DIN 58932-2:1998 Haematology - Determination of the concentration of blood corpuscles in blood - Part 2: Characteristic quantities for erythrocytes (erythrocyte indices)
DIN 58932-2:1998-06 Haematology - Determination of the concentration of blood corpuscles in blood - Part 2: Characteristic quantities for erythrocytes (erythrocyte indices)
DIN 58932-3:2023-07 Haematology - Determination of the concentration of blood corpuscles in blood - Part 3: Reference method for the determination of the concentration of erythrocytes; Text in German and English / Note: Date of issue 2023-06-02*Intended as replacement for...
DIN 58932-4:2003-07 Haematology - Determination of the concentration of blood corpuscles in blood - Part 4: Reference procedure for the determination of the concentration of leucocytes
DIN 58939-1:2000-03 Haemostaseology - Reference plasma - Part 1: Requirements, preparation
DIN 12750:1969-02 Blood dilution pipettes for blood corpuscles counting
DIN 58930:2002-08 Haemostaseology - INR calibration plasmas - Requirements, preparation and use
DIN 58932-1:2023 Haematology - Determination of the concentration of blood corpuscles in blood - Part 1: Blood collection, sample preparation, biological influence factors, interference factors; Text in German and English
DIN 58987:2010-03 Haemostaseology - Reference method for the VWF antigen; Text in German and English
DIN 58932-6:2021 Haematology - Determination of the concentration of blood corpuscles in blood - Part 6: Reference method for the determination of the concentration of CD4 positive lymphocytes; Text in German and English
DIN EN 60601-2-16:2016 Medical electrical equipment - Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment (IEC 60601-2-16:2012); German version EN 60601-2-16:2015
DIN 58932-3:2017 Haematology - Determination of the concentration of blood corpuscles in blood - Part 3: Reference method for the determination of the concentration of erythrozytes; Text in German and English
DIN 58987:2023-04 Haemostaseology - Reference method for the Von Willebrand Factor antigen; Text in German and English / Note: Date of issue 2023-03-03*Intended as replacement for DIN 58987 (2010-03).
DIN 58932-6:2021-08 Haematology - Determination of the concentration of blood corpuscles in blood - Part 6: Reference method for the determination of the concentration of CD4 positive lymphocytes; Text in German and English
DIN 58988:2010-03 Haemostaseology - Reference method for the VWF multimeres; Text in German and English
DIN 58988:2023-04 Haemostaseology - Reference method for the Von Willebrand Factor multimers; Text in German and English / Note: Date of issue 2023-03-03*Intended as replacement for DIN 58988 (2010-03).
DIN EN ISO 23500-3:2019-11 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies (ISO 23500-3:2019); German version EN ISO 23500-3:2019 / Note: To be replaced by DIN EN ISO 23500-3 (2022-12).
DIN EN ISO 23500-3:2022-12 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies (ISO/DIS 23500-3:2022); German and English version prEN ISO 23500-3:2022 / Note: Date of issue 2022-11-18*Inten...
DIN EN ISO 3826-3:2008 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features (ISO 3826-3:2006); English version of DIN EN ISO 3826-3:2008-03
DIN EN ISO 3826-4:2015-12 Plastics collapsible containers for human blood and blood components - Part 4: Apheresis blood bag systems with integrated features (ISO 3826-4:2015); German version EN ISO 3826-4:2015
DIN EN ISO 3826-1:2023-08 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2019 + Amd 1:2023); German version EN ISO 3826-1:2019 + A1:2023
DIN 58987:2023 Haemostaseology - Reference method for the Von Willebrand Factor antigen; Text in German and English
DIN EN ISO 13959:2016 Water for haemodialysis and related therapies (ISO 13959:2014)

ES-UNE, blood

UNE-EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
UNE-EN ISO 8637-2:2019 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8637-2:2018)
UNE-EN IEC 60601-2-16:2019 Medical electrical equipment - Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment (Endorsed by Asociación Española de Normalización in July of 2019.)
UNE-EN ISO 3826-1:2020 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2019)
UNE-EN ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies (ISO 23500-3:2019)
ISO/FDIS 23500-3:2023 Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies
UNE-EN ISO 3826-4:2015 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features (ISO 3826-4:2015)

Lithuanian Standards Office , blood

LST EN 1283-2001 Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
LST EN 60601-2-16+AC-2000 Medical electrical equipment -- Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment (IEC 60601-2-16:1998) )
LST EN ISO 3826-1:2004 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2003)

KR-KS, blood

KS P ISO 8637-2-2022 Extracorporeal systems for blood purification — Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
KS K ISO 16603-2012(2022) Clothing for protection against contact with blood and body fluids－Determination of the resistance of protective clothing materials to penetration by blood and body fluids－Test method using synthetic
KS P ISO 3826-4-2019 Plastics collapsible containers for human blood and blood components — Part 4: Aphaeresis blood bag systems with integrated features
KS C IEC 60601-2-16-2018 Medical electrical equipment — Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
KS P ISO 3826-1-2021 Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers
KS P ISO 8637-2018 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
KS C IEC 60601-2-16-2022 Medical electrical equipment — Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
KS P ISO 23500-3-2021 Preparation and quality management of fluids for haemodialysis and related therapies — Part 3: Water for haemodialysis and related therapies

未注明发布机构, blood

DIN EN 1283:1996 Hemodialyzers, hemodiafilters, hemofilters, hemoconcentrators and associated LJ blood tubing systems
JIS T 3217:2023 Plastic collapsible containers for human blood and blood components
DIN EN ISO 3826-1:2004 Plastic bags for human blood and blood components – Part 1: Conventional bags
BS EN ISO 3826-1:2019 Plastics collapsible containers for human blood and blood components Part 1 : Conventional containers
BS EN ISO 13959:2015 Water for haemodialysis and related therapies
BS EN ISO 3826-3:2007(2008) Plastics collapsible containers for human blood and blood components — Part 3 : Blood bag systems with integrated features

CEN - European Committee for Standardization, blood

EN ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers@ haemodiafilters and haemofilters
EN ISO 23500-3:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 3: Water for haemodialysis and related therapies

AT-ON, blood

ONORM EN 1283-1996 Haemodialysers,haemodiafilters,haemofilters,haemoconcentrators and their extracorporeal circuits
ONORM K 2030-1983 Refrigerators for blood conservation; definitions, requirements, fest

Canadian Standards Association (CSA), blood

CSA Z8637-08-CAN/CSA-2008 Cardiovascular implants and artificial organs ?Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
CSA Z902-04-CAN/CSA-2004 Sang et produits sanguins labiles Premiere Edition
CSA ISO 8637-1:2021 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (Adopted ISO 8637-1:2017, first edition, 2017-11)
CAN/CSA-ISO 8637:2012 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (First Edition)
CSA Z364.1.1/Z364.1.2-94-1994 Hemodialyseurs, Hemofiltres Et Hemoconcentrateurs Deuxieme Edition; Fiche No 1
CAN/CSA-ISO 8638:2013 Implants cardiovasculaires et systèmes extracorporels - Circuit sanguin extracorporel pour les hémodialyseurs, les hémodiafiltres et les hémofiltres (première édition)
CAN/CSA-ISO 8638:2012 Cardiovascular implants and extracorporeal systems — Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (First Edition)
CSA Z902-2004 Blood and Blood Components First Edition; Update No. 1
CSA Z8638-08-CAN/CSA-2008 Cardiovascular implants and artificial organs ?Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters First Edition [Replaced: CSA Z364.1.1/Z364.1.2-94, CSA Z364.1.1/Z364.1.2-94]
CAN/CSA-ISO 8637A:2015 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators AMENDMENT 1: Revision to Figure 2 - Main fitting dimensions of dialysis fluid inlet and outlet ports (First Edition)
CSA C22.2 No.60601-2-16-01-2001 Medical Electrical Equipment - Part 2-16: Particular Requirements for the Safety of Haemodialysis, Haemodiafiltration and Haemofiltration Equipment Second Edition; IEC 60601-2-16:1998
CSA Z364.2.1-2013 Monitoring systems for hemodialysis equipment (Third Edition)
CAN/CSA-ISO 13959:2015 Water for haemodialysis and related therapies (Second Edition)

US-AAMI, blood

ANSI/AAMI/ISO 8637:2010 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
ANSI/AAMI RD16-2007 Cardiovascular implants and artificial organs-Hemodialyzers,hemodiafilters,hemofilters,and hemoconcentrators
ANSI/AAMI RD17-2007 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for hemodialyzers, hemodiafilters and hemofilters
ANSI/AAMI/ISO 8637:2010/A1:2013 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators - Amendment 1: Revision to Figure 2 - Main fitting dimensions of dialysis fluid inlet and outlet ports
AAMI RD62-2006 Water treatment equipment for hemodialysis application
ANSI/AAMI 13959-2014 Water for hemodialysis and related therapies

American Society for Testing and Materials (ASTM), blood

ASTM F1830-97(2017) Standard Practice for Selection of Blood for in vitro Evaluation of Blood Pumps
ASTM F1830-97 Standard Practice for Selection of Blood for In Vitro Evaluation of Blood Pumps
ASTM E788-97(2003) Standard Specification for Pipet, Blood Diluting
ASTM E788-97 Standard Specification for Pipet, Blood Diluting
ASTM E788-97(2008) Standard Specification for Pipet, Blood Diluting
ASTM E788-97(2013) Standard Specification for Pipet, Blood Diluting
ASTM ISO/ASTM 51939-02 Standard Practice for Blood Irradiation Dosimetry
ASTM ISO/ASTM 51939-05(2013) Standard Practice for Blood Irradiation Dosimetry
ASTM E788-97(2019) Standard Specification for Pipet, Blood Diluting
ASTM ISO/ASTM 51939-17(2022) Standard Practice for Blood Irradiation Dosimetry
ASTM ISO/ASTM 51939-17 Standard Practice for Blood Irradiation Dosimetry
ASTM ISO/ASTM 51939-05 Standard Practice for Blood Irradiation Dosimetry
ASTM ISO/ASTM51939-17 Standard Practice for Blood Irradiation Dosimetry
ASTM ISO/ASTM51939-05(2013) Standard Practice for Blood Irradiation Dosimetry
ASTM ISO/ASTM51939-05 Standard Practice for Blood Irradiation Dosimetry
ASTM ISO/ASTM51939-02 Standard Practice for Blood Irradiation Dosimetry

Indonesia Standards, blood

SNI ISO 8638:2012 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
SNI 16-4774-1998 Transfusion equipment for medical use - Blood taking set
SNI ISO 13959:2010 Water for haemodialysis and related therapies

Jilin Provincial Standard of the People's Republic of China, blood

DB22/T 2196-2014 Specifications for quality control of water for hemodialysis and hemodialysis fluid
DB22/T 2915-2018 Technical requirements for blood testing of blood donor dogs
DB22/T 2031-2014 Specifications for Quality Control of Hemodialysis Machines
DB22/T 3258-2021 Specifications for the processing of blood routine cryoagglutination specimens

SE-SIS, blood

SIS SS 87 511 06-1989 Infusion sets for blood

AENOR, blood

UNE-EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8638:2010)
UNE-EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637:2010, including Amendment 1 2013-04-01)
UNE-EN 60601-2-16:1999 MEDICAL ELECTRICAL EQUIPMENT. PART 2-16: PARTICULAR REQUIREMENTS FOR THE SAFETY OF HAEMODIALYSIS, HAEMODIAFILTRATION AND HAEMOFILTRATION EQUIPMENT.
UNE 81594:1992 BIOLOGICAL CONTROL. DETERMINATIO OF ZINC PROTOPORPHYRIN (ZPP) IN BLOOD. METHOD OF DIRECT READING (HEMATOFLUOROMETER).
UNE 111301:1990 REQUIREMENTS OF WATER USED IN HEMODIALYSIS
UNE 111225:1990 EVACUATED TUBES FOR BLOOD SPECIMEN COLLECTION
UNE-EN ISO 3826-1:2013 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2013)

YU-JUS, blood

JUS B.E4.095-1981 Bottles for conservated human blood, derivate of blood, parenteral solution and water for injections
JUS G.F1.050/1-1993 Rubber for medical and pharmaceutical ueses - Rubber bottles closures for conservated human blood, blood derivates, parentheral solutions and water injections - Amendments

TH-TISI, blood

TIS 1298-2012 Sterile plastic containers for human blood and blood components

Standard Association of Australia （SAA）, blood

AS 3864:1997 Medical refrigeration equipment - For the storage of blood and blood products
AS 3864:1997/Amdt 1:1998
AS 3864.1:2012
AS/NZS IEC 60601.2.16:2015
AS/NZS 3200.2.16:1999 Medical electrical equipment - Particular requirements for safety - Haemodialysis, haemodiafiltration and haemofiltration equipment

VN-TCVN, blood

TCVN 7611-2007 Plastics collapsible containers for human blood and blood components
TCVN 7303-2-16-2007 Medical electrical equipment.Part 2-16: Particular requirements for the safety of haemodialysis, haemodiafiltration and haemofiltration equipment

Military Standards (MIL-STD), blood

DOD A-A-53971-1989 CUFF, BLOOD WARMER
DOD A-A-54504-1991 ANALYZER, BLOOD GAS
DOD MIL-B-36970 A-1991 BOX, BLOOD PRODUCTS SHIPPING
DOD A-A-53267 A-1990 ANALYZER, CENTRIFUGAL, HEMATOLOGY
DOD A-A-51963-1987 WEIGHT, BLOOD BAG, WATER BATH (LEAD)
DOD A-A-50989-1985 TUBE, COILED, BLOOD WARMING, (STERILE)
DOD A-A-51995-1987 INFUSOR, PRESSURE, BLOOD COLLECTING-DISPENSING BAG
DOD A-A-53927-1989 INFUSOR, PRESSURE, BLOOD-INTRAVENOUS BAG
DOD A-A-54940-1994 NEEDLE, HYPODERMIC, BLOOD COLLECTING
DOD A-A-53973 B-1993 BAG, BLOOD COLLECTING-DISPENSING-SYSTEM
DOD A-A-54190-1990 HOLDER, BLOOD COLLECTING-DISPENSING BAG
DOD A-A-54844-1993 NEEDLE, HYPODERMIC, BLOOD COLLECTING
DOD A-A-54126-1990 PIPET-DILUENT, BLOOD, LABORATORY
DOD A-A-53924-1989 RINSE SOLUTION, BLOOD GAS ANALYZER
DOD A-A-54872-1993 BLOOD EXCHANGE-TRANSFUSION KIT, DISPOSABLE
DOD A-A-51342-1986 SHAKING MACHINE, LABORATORY, (BLOOD COLLECTING TUBE)
DOD A-A-53423-1988 BAG, BLOOD WARMING (DISPOSABLE)
DOD A-A-53738-1988 MEMBRANE KIT, BLOOD GAS ANALYZER (PO2)
DOD A-A-53865 A-1993 HOLDER, BLOOD COLLECTING TUBE (PLASTIC)
DOD A-A-54473-1991 CENTRIFUGE, LABORATORY (HEMATOLOGY)
DOD A-A-54092-1990 TUBE, BLOOD COLLECTING (VACUUM WITH SEPARATOR GEL)
DOD A-A-54964-1994 MONITORING SET, ARTERIAL BLOOD GAS SAMPLING AND PRESSURE
DOD A-A-51551 A-1987 BLOOD RECIPIENT SET, INDIRECT TRANSFUSION [Use In Lieu Of: DOD A-A-0051551]
DOD A-A-54089 A-1992 BLOOD RECIPIENT SET, INDIRECT TRANSFUSION (DISPOSABLE)
DOD A-A-51823 A-1988 TUBE, CENTRIFUGAL HEMATOLOGY [Use In Lieu Of: DOD A-A-0051823]
DOD A-A-51879 A-1988 TUBE, CENTRIFUGAL HEMATOLOGY [Use In Lieu Of: DOD A-A-0051879]

NATO - North Atlantic Treaty Organization, blood

AMEDP-12(A)-2003 NATO BLOOD BROCHURE (To obtain please contact your national Defense Standardization Office or the NATO Standardization Office website: http:/ so.nato.int so@ Phone: +32 (0)2 – 707 5556@ email: nso@nso.nato.int. For additional information please see the IH
AMEDP-12-1998 NATO BLOOD BROCHURE (To obtain please contact your national Defense Standardization Office or the NATO Standardization Office website: http:/ so.nato.int so@ Phone: +32 (0)2 – 707 5556@ email: nso@nso.nato.int. For additional information please see the IH
STANAG 2408-1998 NATO Blood Brochure - AMedP-12 (ED 1; To obtain please contact your national Defense Standardization Office or the NATO Standardization Office website: http:/ so.nato.int so@ Phone: +32 (0)2 – 707 5556@ email: nso@nso.nato.int. For additional information
STANAG 2939-2010 MINIMUM REQUIREMENTS FOR BLOOD@ BLOOD DONORS AND ASSOCIATED EQUIPMENT (ED 5; To obtain please contact your national Defense Standardization Office or the NATO Standardization Office website: http:/ so.nato.int so@ Phone: +32 (0)2 – 707 5556@ email: nso@ns

国家药监局, blood

YY 0054-2023 hemodialysis equipment
YY/T 1631.1-2018 Determination of compatibility between blood transfusion sets and blood components Part 1: Assessment of blood component residues
YY/T 1631.2-2020 Determination of compatibility of blood transfusion sets and blood components Part 2: Assessment of blood component damage
YY/T 1834-2022 X-ray blood irradiation equipment
YY/T 0701-2021 Calibrators for blood analyzers
YY/T 0464-2019 Disposable hemoperfusion device
YY/T 1730-2020 Disposable hemodialysis catheter

Professional Standard - Hygiene , blood

WS 399-2012 Standards for blood storage
WS/T 400-2012 Requirements for blood transportation
WS/T 400-2023 blood transport standards
WS/T 399-2023 blood storage standards

未注明发布机构, blood

DIN EN 1283:1996 Hemodialyzers, hemodiafilters, hemofilters, hemoconcentrators and associated LJ blood tubing systems
JIS T 3217:2023 Plastic collapsible containers for human blood and blood components
DIN EN ISO 3826-1:2004 Plastic bags for human blood and blood components – Part 1: Conventional bags
BS EN ISO 3826-1:2019 Plastics collapsible containers for human blood and blood components Part 1 : Conventional containers
BS EN ISO 13959:2015 Water for haemodialysis and related therapies
BS EN ISO 3826-3:2007(2008) Plastics collapsible containers for human blood and blood components — Part 3 : Blood bag systems with integrated features

American National Standards Institute （ANSI), blood

ANSI/AAMI/ISO 8637AMD 1:2012 Hemodialyzers, haemodiafilters, haemofilters and haemoconcentrators - Amendment 1: Revision to Figure 2 - Main fitting dimensions of dialysis fluid inlet and outlet ports
ANSI/AAMI/ISO 8638:2010 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
ANSI/AAMI/IEC 60601-2-16,Ed. 4:2012 Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
ANSI/AAMI/ISO 13959:2009 Water for hemodialysis and related therapies
ANSI/AAMI/ISO 13958:2009 Concentrates for hemodialysis and related therapies
ANSI/ASTM E1939:2004 Practice for Blood Irradiation Dosimetry
ANSI/AAMI RD47:2002/A1-2003 Reuse of Hemodialyzers Amendment 1

Group Standards of the People's Republic of China, blood

T/CSBME 057-2022 Adsorption resin for hemoperfusion or plasma perfusion devices
T/CSBT 001-2019 Guideline for Haemovigilance
T/JPMA 007-2020 Guidelines on the use of irradiated blood components
T/ZSA 71-2019 Specifications for blood purification facility configuration
T/NBPIA 001-2020 Specifications for blood purification facility configuration
T/CSBT 002-2019 Guideline for reentry of reactive blood donors in blood screening test
T/NBPIA 007-2021 Classification of hemodialyzer clinical performance
T/NBPIA 008-2021 Specifications for quality control in blood purification facilities
T/CNMIA 0002-2019 Evaluation criteria for independent hemodialysis centers
T/NBPIA 003-2020 Technical Specification for quality of hemodialysis water
T/QDAS 079-2022 Smart Blood Management Platform Construction Guide
T/NBPIA 010-2023 Clinical Practice Guidelines for Home Hemodialysis
T/SHDSGY 026-2023 Disposable blood extracorporeal circulation tubing
T/CAME 38-2021 Performance validation of nucleic acid testing in blood screening
T/CAMDI 103-2023 Hemodialysis IV catheter for single use
T/CAME 48-2022 Centre concentrate delivery system for haemodialysis
T/QYSJLXH 002-2019 Calibration specification for temperature parameters of blood refrigerator
T/CSBT 004-2019 Quality monitoring indicators of blood testing laboratory in blood transfusion service
T/CAME 46-2022 Essential requirements for engineering technical personnel of hemodialysis

RO-ASRO, blood

STAS 5442-1987 RUBBER STOPPERS FOR BLOOD, PLASMA AND AQUEOUS PERFUSABLE SOLUTION VIALS
STAS 5328-1989 GLASS BOTTLES FOR BLOOD
STAS 5877-1958
STAS 11326/6-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND A QUEOUS SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Inocuity checking up
STAS 5327-1978 SCREW THREAD FOR GLASS BOTTLES FOR BLOOD AND PLASMA
STAS 11327/3-1983 RUBBER STOPPERS FOR BLOOD,PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS pH aqueous extract checking out
STAS 11326/2-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND AQUEOUS SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Pyrogenic impurities checking up
STAS 11327/9-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Organic substances determination
STAS 11327/2-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Apparence, smell and taste checking out
STAS 11326/4-1984 RUBBER STOPPERS FOR RECIPIENTS OF BLOOD, PLASMA AND AQUEOUS SOLUTIONS FOR INJECTIONS AND PERFUSIONS Hcmolityc impurities checking up
STAS 11327/8-1983 RUBBER STOPPERS FOR BLOOD,PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS etermination of volatile sulphides
STAS 11326/3-1984 RUBBER STOPPERS FOR INJECTABLE AND PERFUSABLE BLOOD, PLASMA AND AQUEOUS SOLUTION BOTTLES Toxicity checking up

国家市场监督管理总局、中国国家标准化管理委员会, blood

GB 14232.1-2020 Plastics collapsible containers for human blood and blood components—Part 1: Conventional containers
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 38576-2020 Collection and processing of human blood biomaterial
GB 14232.4-2021 Plastics collapsible containers for human blood and blood components—Part 4: Aphaeresis blood bag systems with integrated features
GB/T 15593-2020 Plasticized poly(vinyl chloride) compounds for transfusion (infusion) equipment

Professional Standard - Agriculture, blood

546药典化学药和生物制品卷-2010 Chapter 7 Drugs for the Urinary System Section 2 Dialysate for Blood Purification and Replacement Fluid Hemodialysate
547药典化学药和生物制品卷-2010 Chapter 7 Drugs for the Urinary System Section 2 Dialysate and Replacement Fluid for Blood Purification Hemofiltration Replacement Fluid
8药典三部-2010 General headings Human plasma for the production of blood products
20药典三部-2020 General principles of biological products Human plasma for the manufacture of blood products
23药典三部-2015 General principles of biological products Human plasma for the manufacture of blood products
1300药典化学药和生物制品卷-2010 Chapter 18 Biological Products 3. Blood Products Human Albumin

National Metrological Technical Specifications of the People's Republic of China, blood

JJF 1316-2011 Calibration Specification for Blood Viscometers
JJF 1633-2017 Calibration Specification for Hemoperfusion Equipment
JJF 1353-2012 Calibration Specification for Hemodialysis Equipment
JJF 1541-2015 Calibration Specification for Hemodialysis Equipment Tester
JJF 1844-2020 Calibration Specification for Continuous Blood Purification Equipment

North Atlantic Treaty Organization Standards Agency, blood

STANAG 2408-2003 NATO BLOOD BROCHURE - AMedP-12(A)
STANAG 2939-2000 MEDICAL REQUIREMENTS FOR BLOOD, BLOOD DONORS AND ASSOCIATED EQUIPMENT

Sichuan Provincial Standard of the People's Republic of China, blood

DB51/T 1266-2011 Heartbeat and blood circulation model
DB51/T 1207-2011 Diagnosis technical rules for silkworm blood type pus disease

国家药品监督管理局, blood

YY 0645-2018 Continuous blood purification equipment

International Electrotechnical Commission (IEC), blood

IEC 60601-2-16/COR1:2008 Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
IEC 60601-2-16:2012 Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
IEC 60601-2-16:2018 RLV Medical electrical equipment - Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment
IEC 60601-2-16:1998 Medical electrical equipment - Part 2-16: Particular requirements for safety of haemodialysis, haemodiafiltration and haemofiltration equipment

CENELEC - European Committee for Electrotechnical Standardization, blood

EN 60601-2-16:2015 Medical electrical equipment - Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis@ haemodiafiltration and haemofiltration equipment
EN 60601-2-16:1998 Medical Electrical Equipment Part 2-16: Particular Requirements for the Safety of Haemodialysis@ Haemodiafiltration and Haemofiltration Equipment (Incorporating Corrigendum December 1999)

European Committee for Electrotechnical Standardization（CENELEC）, blood

EN IEC 60601-2-16:2019 Medical electrical equipment - Part 2-16: Particular requirements for the basic safety and essential performance of haemodialysis, haemodiafiltration and haemofiltration equipment

Jiangsu Provincial Standard of the People's Republic of China, blood

DB32/T 3545.6-2023 Blood purification treatment technology management Part 6: Specifications for the establishment of independent blood purification centers
DB32/T 3545.1-2019 Technical management of blood purification therapy part 1 Infection management norms in blood purification therapy institutions
DB32/T 3545.5-2023 Blood Purification Treatment Technology Management Part 5: Emergency Procedures for Blood Purification Medical Institutions
DB32/T 3545.2-2020 Technical management of blood purification treatment part 2 Quality control specification for hemodialysis water treatment system
DB32/T 3545.4-2021 Technical Management of Blood Purification Therapy Part 4: Medical Quality Management Standards for Blood Purification Medical Institutions
DB32/T 3545.3-2021 Technical management of blood purification therapy part 3: training norms for medical staff in blood purification medical institutions

PL-PKN, blood

PN A85701-1964 Blood of slaughter anlmals and derived

卫生健康委员会, blood

WS/T 661-2020 Venous blood specimen collection guide
WS/T 796-2022 Guidelines for blood management in perioperative patients
WS/T 789-2021 Blood product labeling and identification code standards

农业农村部, blood

NY/T 3471-2019 Technical specifications for blood collection from livestock and poultry

IEC - International Electrotechnical Commission, blood

IEC 60601-2-16:2008 Medical electrical equipment – Part 2-16: Particular requirements for basic safety and essential performance of haemodialysis@ haemodiafiltration and haemofiltration equipment (Edition 3.0)

Professional Standard - Public Safety Standards, blood

GA 656-2006 Detection method for ABO blood type in human blood(stains). Hemagglutination test, elution test
GA/T 842-2019 Examination methods for ethanol concentration in blood
GA/T 842-2009 How to test blood alcohol content

Defense Logistics Agency, blood

DLA NNN-B-300 A-1977 BLOOD COLLECTING-CULTURE UNIT, LABORATORY

Beijing Provincial Standard of the People's Republic of China, blood

DB11/T 486-2021 Basic data set of blood management information

CU-NC, blood

NC 57-60-1985 Blood and saliva Ejector Quality Specifications

HU-MSZT, blood

National Metrological Verification Regulations of the People's Republic of China, blood

JJG 553-1988 Verification Regulation of Blood Gas Acid-Base Analyser

国家技术监督局, blood

GB/T 15593-1995 Plasticized polyvinyl chloride (PVC) compounds for transfusion (infusion) equipment

Anhui Provincial Standard of the People's Republic of China, blood

DB34/T 4240-2022 Service Specifications for Third-Party Blood Testing Institutions

Shaanxi Provincial Standard of the People's Republic of China, blood

DB61/T 944-2015 Information coding and symbol identification of blood preparations

中华人民共和国国家卫生和计划生育委员会, blood

WS/T 226-2002 Guidelines for blood glucose testing by using portable blood glucose meter
WS/T 92-1996 Blood.Determination of zinc protoporphyrin.Hematofluorometer method

Professional Standard - Commodity Inspection, blood

SN/T 0323.3-2007 Rules for the inspection of medical equipment for import and export.Part 3:Plastic collapsible containers for human blood.Blood components conventional containers
SN/T 4352-2015 Inspection and quarantine procedure for feeding blood products

National Health Commission of the People's Republic of China, blood

WS/T 806-2022 Basic technical standards for clinical blood and body fluid testing