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blood blood sample

blood blood sample, Total:498 items.

In the international standard classification, blood blood sample involves: Biology. Botany. Zoology, Medical equipment, Meat, meat products and other animal produce, Laboratory medicine, Sacks. Bags, Medical sciences and health care facilities in general, Hospital equipment, Refrigerating technology, Shop fittings, Veterinary medicine, First aid, Character sets and information coding, Protective equipment, Precision mechanics, Vocabularies, Protection against crime, Aircraft and space vehicles in general, Pharmaceutics, Pipeline components and pipelines, Education, Plastics, Food products in general, Installations in buildings.


ES-AENOR, blood blood sample

国家市场监督管理总局、中国国家标准化管理委员会, blood blood sample

  • GB/T 38576-2020 Collection and processing of human blood biomaterial
  • 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 14232.1-2020 Plastics collapsible containers for human blood and blood components—Part 1: Conventional containers
  • GB 14232.4-2021 Plastics collapsible containers for human blood and blood components—Part 4: Aphaeresis blood bag systems with integrated features

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

  • GB/T 13074-1991 Terms of blood purification--Hemodialysis and hemofiltration
  • GB/T 21278-2007 Refrigerators for conserved blood
  • 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/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 14232.3-2011 Plastics collapsible containers for human blood and blood components. Part 3:Blood bag systems with integrated features

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

  • 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

German Institute for Standardization, blood blood sample

  • 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 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 58934-1:1997 Haematology - Control material for the CBC - Part 1: Control bloods
  • DIN 12750:1969 Blood dilution pipettes for blood corpuscles counting
  • 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 58931:2010 Haematology - Determination of haemoglobin concentration in blood - Reference method; Text in German and English
  • DIN 58931:1995 Haematology - Determination of haemoglobin concentration in blood - Reference method
  • DIN EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
  • 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 12750:1969-02 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 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 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 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 58934-1:1997-12 Haematology - Control material for the CBC - Part 1: Control bloods
  • DIN 58932-3:1994 Haematology; determination of the concentration of blood corpuscles in blood; determination of the concentration of erythrocytes; reference method
  • 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 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 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 58932-5:2007 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 58932-1:2012 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 58932-1:1996 Haematology - Determination of the concentration of blood corpuscles in blood - Part 1: Blood collection, sample preparation, biological influence factors, interference factors
  • 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 58932-4:2003 Haematology - Determination of the concentration of blood corpuscles in blood - Part 4: Reference procedure for the determination of the concentration of leucocytes
  • DIN 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 EN 12022:1999 Blood gas exchangers; German version EN 12022:1999
  • 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 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 58930:2002-08 Haemostaseology - INR calibration plasmas - Requirements, preparation and use
  • DIN 58939-1:2000-03 Haemostaseology - Reference plasma - Part 1: Requirements, preparation
  • 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 58369:1996 Transfusion, infusion - Disposable hanging devices for bottles for transfusion and infusion - Requirements, test
  • 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 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 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 58910-4:2000-03 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 4: Reference measurement procedure for the determination in capillary blood
  • DIN EN ISO 3826-4:2015 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 3826-3:2008 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 23500-4:2019-11 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO 23500-4:2019); German version EN ISO 23500-4:2019 / Note: To be replaced by DIN EN ISO 23500-4 (202...
  • DIN EN ISO 23500-4:2022-12 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO/DIS 23500-4:2022); German and English version prEN ISO 23500-4:2022 / Note: Date of issue 2022-11-1...
  • DIN 58933-1:1995 Haematology - Procedure for determining the volume fraction of erythrocytes (packed cell volume) in blood - Part 1: Reference method based on centrifugation
  • DIN 58910-1:2016-02 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood; Text in German and English
  • DIN 58910-3:2000-03 Haemostaseology - Determination of the thromboplastin (prothrombin) time - Part 3: Reference measurement procedure for the determination in citrated capillary blood
  • DIN EN ISO 3826-3:2008-03 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features (ISO 3826-3:2006); German version EN ISO 3826-3:2007
  • DIN 58914-1:2000-03 Haemostaseology - Determination of thrombin time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood

Korean Agency for Technology and Standards (KATS), blood blood sample

  • 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 4907-2011 Haemodialysers, haemofilters and haemoconcentrators
  • KS P ISO 8638-2012(2017) Cardiovascular implants and extracorporeal systems －Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • KS P ISO 8637:2018 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • 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 C IEC 60601-2-16:2002 Haemodialysis, haemodiafiltration and haemofiltration equipment
  • 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 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(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 3826-1:2021 Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers
  • KS P ISO 23500-4:2021 Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapies

International Organization for Standardization (ISO), blood blood sample

  • 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 8637:2004 Cardiovascular implants and artificial organs - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 8637:2010 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • 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/DIS 8637-2 Extracorporeal systems for blood purification — Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 3826:1993 Plastics collapsible containers for human blood and blood components
  • 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 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 3826-3:2006 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 3826-1:2003 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers
  • ISO 18242:2016 Cardiovascular implants and extracorporeal systems - Centrifugal blood pumps
  • ISO 3826-1:2013 Plastics collapsible containers for human blood and blood components.Part 1: Conventional containers
  • ISO 3826-4:2015 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features
  • ISO/DIS 23500-4 Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapies
  • ISO 8637-3:2018 Extracorporeal systems for blood purification - Part 3: Plasmafilters
  • ISO 4822:1981 Single use blood specimen containers up to 25 ml capacity
  • ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapies
  • ISO/FDIS 23500-4:2011 Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapies
  • ISO 3826-1:2019/Amd 1:2023 Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers — Amendment 1
  • ISO 11663:2014 Quality of dialysis fluid 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 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

Japanese Industrial Standards Committee (JISC), blood blood sample

  • 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 3254:2007 Single-use syringes for blood gas specimen collection
  • JIS T 3254:2013 Single-use syringes for blood gas specimen collection
  • 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 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 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
  • 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 3232:2011 Blood filters for cardiopulmonary bypass systems
  • JIS T 3232:2016 Blood filters for cardiopulmonary bypass systems
  • 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 1603:1995 Electric motor driven blood pump for cardiopulmonary bypass

European Committee for Standardization (CEN), blood blood sample

  • 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 3826-1:2003 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 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

Professional Standard - Medicine, blood blood sample

  • 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 0267-2016 Extracorporeal circulation blood circuit of blood purification device for hemodialysis and related treatment
  • 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/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 0054-2010 Haemodialysis equipment
  • YY 0790-2010 Hemoperfusion equipment
  • YY 0267-1995 Extracorporeal blood circuit for blood purification devices
  • YY/T 1545-2017 Evaluation of concentrates for hemodialysis in connection with hemodialysis equipment
  • YY/T 0031-1990 Silicone rubber infusion (blood) tube
  • YY/T 0456.2-2014 Reagents for hematology analyzer.Part 2:Hemolysin
  • YY/T 1288-2015 Nylon blood filter nets for transfusion equipments for single use
  • YY 0645-2008 Continuous blood purification equipment
  • YY 91020-1999 Needles used for transfusion and infusion
  • YY 0267-2008 Cardiovascular implants and artificial organs.Extracorporeal blood circuit for blood purification devices
  • 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/T 0456.1-2014 Reagents for hematology analyzer.Part 1:Rinse
  • YY/T 1414-2016 Liquid line solenoid valve for haemodialysis equipment
  • YY 0572-2015 Water for haemodialysis and related therapies
  • YY 0572-2005 Water for haemodialysis and related therapies

British Standards Institution (BSI), blood blood sample

  • BS EN ISO 8637-1:2020 Extracorporeal systems for blood purification. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BS EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems. 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
  • 12/30254337 DC BS ISO 8637 AMD1. Cardiovascular implants and extracorporeal systems. 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
  • 16/30331650 DC BS EN ISO 8637-1. Extracorporeal systems for blood purification. Part 1. 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
  • 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 EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • 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 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
  • 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 12022:1999 Blood-gas exchangers
  • BS EN ISO 3826-1:2013 Plastics collapsible containers for human blood and blood components. Conventional containers
  • BS EN ISO 3826-4:2015 Plastics collapsible containers for human blood and blood components. Aphaeresis blood bag systems with integrated features
  • BS EN ISO 3826-1:2019+A1:2023 Plastics collapsible containers for human blood and blood components - Conventional containers
  • BS ISO 18242:2016 Cardiovascular implants and extracorporeal systems. Centrifugal blood pumps
  • 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 2463-1:1990 Transfusion equipment for medical use - Specification for collapsible containers for blood and blood components
  • BS ISO 13959:2014 Water for haemodialysis and related therapies

RU-GOST R, blood blood sample

  • GOST 33674-2015 Blood and processed products. Specifications
  • GOST R 52938-2008 Blood and blood components. Containers with blood or blood components. Labeling
  • 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 ISO 8638-1999 Extracorporeal blood circuit for haemodialysers, haemofilters and haemoconcentrators. Technical requirements and test methods
  • GOST ISO 8637-2012 Haemodialysers, haemofiltres and haemoconcentrators. Technical requirements and test methods
  • 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 8637-1999 Haemodialysers, haemofilters and haemoconcentrators. Technical requirements and test methods
  • 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 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

US-FCR, blood blood sample

IN-BIS, blood blood sample

CZ-CSN, blood blood sample

未注明发布机构, blood blood sample

  • 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
  • DIN EN 14252:2004 In-vitro diagnostics – disposable vessels for human specimens with the exception of blood samples; German version EN 14254:2004
  • BS EN ISO 3826-3:2007(2008) Plastics collapsible containers for human blood and blood components — Part 3 : Blood bag systems with integrated features
  • DIN EN ISO 8362-5:2014 Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical use
  • BS EN ISO 3826-1:2019 Plastics collapsible containers for human blood and blood components Part 1 : Conventional containers
  • BS EN ISO 11663:2015 Quality of dialysis fluid for haemodialysis and related therapies

Danish Standards Foundation, blood blood sample

  • 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 3826-3:2008 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features
  • DS/EN ISO 3826-1:2013 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers

ES-UNE, blood blood sample

  • 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 3826-4:2015 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features (ISO 3826-4:2015)
  • 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 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies (ISO 23500-4:2019)

Association Francaise de Normalisation, blood blood sample

  • 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*NF EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • 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 S93-303:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • 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 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 EN ISO 1135-3:2017 Matériel de transfusion à usage médical - Partie 3 : appareils non réutilisables pour prélèvement sanguin
  • NF EN ISO 3826-1:2019 Poches en plastique souple pour le sang et les composants du sang - Partie 1 : poches conventionnelles
  • 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 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 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 S93-230-1:2013 Plastics collapsible containers for human blood and blood components - Part 1: conventional containers
  • NF S93-315:2008 Fluids for hemodialysis - Requirements and user recommendations
  • 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

Lithuanian Standards Office , blood blood sample

  • 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 3826-3:2008 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features (ISO 3826-3:2006)

Canadian Standards Association (CSA), blood blood sample

  • CSA Z8637-08-CAN/CSA-2008 Cardiovascular implants and artificial organs ?Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • CAN/CSA-ISO 8637:2012 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (First Edition)
  • 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 Z902-04-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)
  • CSA Z364.1.1/Z364.1.2-94-1994 Hemodialyseurs, Hemofiltres Et Hemoconcentrateurs Deuxieme Edition; Fiche 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]
  • CSA Z902-2004 Blood and Blood Components First Edition; Update No. 1
  • 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
  • CAN/CSA-ISO 13958:2015 Concentrates for haemodialysis and related therapies (Second Edition)

US-AAMI, blood blood sample

  • 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
  • ANSI/AAMI 11663-2014 Quality of dialysis fluid for haemodialysis and related therapies

KR-KS, blood blood sample

  • KS P ISO 8637-2-2022 Extracorporeal systems for blood purification — Part 2: Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • KS P ISO 8637-2018 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • 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 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 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 P ISO 3826-1-2021 Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers
  • KS P ISO 8637-3-2022 Extracorporeal systems for blood purification Part 3: Plasmafilters
  • KS P ISO 23500-4-2021 Preparation and quality management of fluids for haemodialysis and related therapies — Part 4: Concentrates for haemodialysis and related therapies

SE-SIS, blood blood sample

CEN - European Committee for Standardization, blood blood sample

  • EN ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers@ haemodiafilters and haemofilters
  • EN ISO 23500-4:2019 Preparation and quality management of fluids for haemodialysis and related therapies - Part 4: Concentrates for haemodialysis and related therapies

AT-ON, blood blood sample

  • ONORM EN 1283-1996 Haemodialysers,haemodiafilters,haemofilters,haemoconcentrators and their extracorporeal circuits

Indonesia Standards, blood blood sample

AENOR, blood blood sample

  • 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 111225:1990 EVACUATED TUBES FOR BLOOD SPECIMEN COLLECTION
  • 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-EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
  • UNE-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)

American Society for Testing and Materials (ASTM), blood blood sample

  • 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 E734-80(2010) Standard Specification for Disposable Glass Blood Sample Capillary Tube (Microhematocrit)
  • 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 F1830-97(2005) Standard Practice for Selection of Blood for in vitro Evaluation of Blood Pumps
  • ASTM F2172-02 Standard Specification for Blood/Intravenous Fluid/Irrigation Fluid Warmers
  • ASTM F2172-02(2011) Standard Specification for Blood/Intravenous Fluid/Irrigation Fluid Warmers

HU-MSZT, blood blood sample

Standard Association of Australia （SAA）, blood blood sample

American National Standards Institute （ANSI), blood blood sample

  • ANSI/AAMI/ISO 8638:2010 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • 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/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 11663:2009 Quality of dialysis fluid for haemodialysis and related therapies

YU-JUS, blood blood sample

  • 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

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

  • 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 3258-2021 Specifications for the processing of blood routine cryoagglutination specimens

卫生健康委员会, blood blood sample

TH-TISI, blood blood sample

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

RO-ASRO, blood blood sample

  • STAS 11326/6-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND A QUEOUS SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Inocuity checking up
  • STAS 11326/3-1984 RUBBER STOPPERS FOR INJECTABLE AND PERFUSABLE BLOOD, PLASMA AND AQUEOUS SOLUTION BOTTLES Toxicity checking up
  • STAS 5442-1987 RUBBER STOPPERS FOR BLOOD, PLASMA AND AQUEOUS PERFUSABLE SOLUTION VIALS
  • STAS 11327/3-1983 RUBBER STOPPERS FOR BLOOD,PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS pH aqueous extract checking out
  • STAS 5327-1978 SCREW THREAD FOR GLASS BOTTLES FOR BLOOD AND PLASMA
  • 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 11326/8-1985 RUBBER STOPPERS FOR BLOOD, PLASMA AND INJECTABLE AND PERFUSABLE AQUEOUS SOLUTIONS Microbiological checking up of poisonous substances with antibacterian action
  • STAS 5328-1989 GLASS BOTTLES FOR BLOOD
  • STAS 5877-1958
  • STAS 11326/4-1984 RUBBER STOPPERS FOR RECIPIENTS OF BLOOD, PLASMA AND AQUEOUS SOLUTIONS FOR INJECTIONS AND PERFUSIONS Hcmolityc impurities checking up
  • STAS 11327/2-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Apparence, smell and taste checking out
  • STAS 11327/8-1983 RUBBER STOPPERS FOR BLOOD,PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS etermination of volatile sulphides
  • STAS 11327/4-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Determination of oxidoreduction substances of aqueous extract
  • STAS 11327/5-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Determination of heavy metals and zinc of aqueous extract

Professional Standard - Hygiene , blood blood sample

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

  • WST 359:2011 Guidelines for the Collection and Processing of Blood Specimens for Plasma Coagulation Tests
  • WS/T 806-2022 Basic technical standards for clinical blood and body fluid testing

International Electrotechnical Commission (IEC), blood blood sample

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

CENELEC - European Committee for Electrotechnical Standardization, blood blood sample

  • 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 blood sample

  • 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

VN-TCVN, blood blood sample

  • 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

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

IEC - International Electrotechnical Commission, blood blood sample

  • 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)

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

  • T/CSBME 057-2022 Adsorption resin for hemoperfusion or plasma perfusion devices
  • T/CRHA 006-2022 Specification for mononuclear cell resource storage in healthy blood donors Part 3：Detection of donor blood samples
  • T/CSBT 002-2019 Guideline for reentry of reactive blood donors in blood screening test
  • T/CSBT 004-2019 Quality monitoring indicators of blood testing laboratory in blood transfusion service
  • T/CSBT 001-2019 Guideline for Haemovigilance
  • T/JPMA 007-2020 Guidelines on the use of irradiated blood components
  • T/CAME 46-2022 Essential requirements for engineering technical personnel of hemodialysis
  • T/CSBT 007-2019 Requirements for external quality assessment of blood screening laboratory
  • T/ZSA 71-2019 Specifications for blood purification facility configuration
  • T/NBPIA 001-2020 Specifications for blood purification facility configuration
  • T/GDC 169-2022 Disposable plastic serological pipet

国家药监局, blood blood sample

  • 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 0054-2023 hemodialysis equipment
  • YY/T 1834-2022 X-ray blood irradiation equipment
  • YY/T 0701-2021 Calibrators for blood analyzers
  • YY/T 1856-2023 General safety requirements for blood, intravenous solution, and lavage fluid warmers
  • YY/T 0464-2019 Disposable hemoperfusion device

Military Standards (MIL-STD), blood blood sample

NATO - North Atlantic Treaty Organization, blood blood sample

  • 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 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
  • 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

Professional Standard - Agriculture, blood blood sample

未注明发布机构, blood blood sample

  • 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
  • DIN EN 14252:2004 In-vitro diagnostics – disposable vessels for human specimens with the exception of blood samples; German version EN 14254:2004
  • BS EN ISO 3826-3:2007(2008) Plastics collapsible containers for human blood and blood components — Part 3 : Blood bag systems with integrated features
  • DIN EN ISO 8362-5:2014 Transfusion, infusion and injection, and blood processing equipment for medical and pharmaceutical use
  • BS EN ISO 3826-1:2019 Plastics collapsible containers for human blood and blood components Part 1 : Conventional containers
  • BS EN ISO 11663:2015 Quality of dialysis fluid for haemodialysis and related therapies

Zhejiang Provincial Standard of the People's Republic of China, blood blood sample

  • DB33/T 918.6-2021 Blood Information System Basic Construction Specification Part 6: Basic Data Set for Information Sharing between Blood Stations and Plasmapheresis Stations
  • DB33/T 918.2-2014 Blood information system basic construction specification part 2: basic data set of blood bank information system
  • DB33/T 918.1-2014 Basic Construction Specifications of Blood Information System Part 1: Basic Functional Specifications of Blood Station Information System
  • DB33/T 918.4-2021 Basic Construction Specifications for Blood Information System Part 4: Basic Data Sets for Information Sharing between Blood Stations and Hospitals

中华人民共和国国家卫生和计划生育委员会, blood blood sample

  • 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

North Atlantic Treaty Organization Standards Agency, blood blood sample

Professional Standard - Public Safety Standards, blood blood sample

  • GA 656-2006 Detection method for ABO blood type in human blood(stains). Hemagglutination test, elution test
  • GA 473-2004 Serum product of anti-human semen
  • GA/T 2073-2023 Forensic sciences—Examination methods for carboxyhaemoglobin in blood samples—Spectrophotometry

US-CLSI, blood blood sample

  • CLSI H18-A4-2010 Procedures for the Handling and Processing of Blood Specimens for Common Laboratory Tests

Guangdong Provincial Standard of the People's Republic of China, blood blood sample

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

  • JJF 1316-2011 Calibration Specification for Blood Viscometers
  • JJF 1633-2017 Calibration Specification for Hemoperfusion Equipment
  • JJF 1353-2012 Calibration Specification for Hemodialysis Equipment

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

国家药品监督管理局, blood blood sample

Professional Standard - Commodity Inspection, blood blood sample

  • 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

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

  • 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 4413-2022 Application specification for radio frequency identification (RFID) technology in qualified blood bank of blood station

PL-PKN, blood blood sample

农业农村部, blood blood sample

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

GOSTR, blood blood sample

  • GOST R EN 14254-2010 In vitro diagnostic medical devices. Single-use receptacles for the collection of specimens, other than blood, from humans

Defense Logistics Agency, blood blood sample

  blood, animal blood, blood analysis, Blood purification, blood circuit, blood disease, blood test, blood alcohol, blood circuit, blood centrifugation, blood centrifugation, blood test, specimen blood, blood instrument, blood concentration, blood content, blood sample, blood flow samples, blood sample, blood blood sample.

 



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