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blood detector

blood detector, Total:498 items.

In the international standard classification, blood detector involves: Veterinary medicine, Medical equipment, Laboratory medicine, Protection against crime, Medical sciences and health care facilities in general, Sacks. Bags, Precision mechanics, Aircraft and space vehicles in general, Farming and forestry, Protective equipment, Biology. Botany. Zoology, Meat, meat products and other animal produce, Plastics, Geology. Meteorology. Hydrology, Water quality, Acoustics and acoustic measurements, Radiation measurements, Applications of information technology, Animal feeding stuffs, Law. Administration, Graphical symbols, Measurement of volume, mass, density, viscosity, Measurement of fluid flow, Microbiology, Optics and optical measurements, Analytical chemistry, Metrology and measurement in general, HEALTH CARE TECHNOLOGY, Fluid power systems, Occupational safety. Industrial hygiene, Vocabularies.


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

  • DB22/T 2915-2018 Technical requirements for blood testing of blood donor dogs
  • DB22/T 2921-2018 PCR method for detection of A/B/J subgroups of avian leukosis
  • DB22/T 3049-2019 Determination of Six Mushroom Toxins in Blood and Urine by Liquid Chromatography-Tandem Mass Spectrometry

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

  • 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
  • CNS 5397-1980 Method of Test of Filters for Hydraulic Use
  • CNS 11749-1986 Glossary of Terms Related to Nondestructive Testing (Liquid Penetrant Testing Terms)

Japanese Industrial Standards Committee (JISC), blood detector

  • 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 3250:2022 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 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 3254:2007 Single-use syringes for blood gas specimen collection
  • JIS T 3254:2013 Single-use syringes for blood gas specimen collection

European Committee for Standardization (CEN), blood detector

  • 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 7199:2014 Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
  • EN ISO 3826-1:2003 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers ISO 3826-1:2003
  • EN ISO 7199:2017 Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
  • EN ISO 3826-3:2007 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated
  • EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)
  • 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)
  • EN ISO 7199:2017/A1:2020 Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) - Amendment 1: Connectors (ISO 7199:2016/Amd 1:2020)
  • EN ISO 20186-3:2019 Molecular in-vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma (ISO 20186-3:2019)
  • 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)
  • CEN EN ISO 3826-3:2007 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features (ISO 3826-3:2006)
  • 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 (ISO 3826-2:2008)

International Organization for Standardization (ISO), blood detector

  • ISO 8637:1989 Haemodialysers, haemofilters and haemoconcentrators
  • ISO 8638:1989 Extracorporeal blood circuit for haemodialysers, 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 8637:2004 Cardiovascular implants and artificial organs - Haemodialysers, haemodiafilters, 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 8637:2010 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 8637-1:2017 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • ISO 8638:2004 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: 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 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 7199:2009 Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
  • ISO 7199:2016 Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
  • ISO 7199:1996 Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators)
  • ISO 3826-1:2019/Amd 1:2023 Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers — Amendment 1
  • ISO 3826-3:2006 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features
  • ISO 8637-3:2018 Extracorporeal systems for blood purification - Part 3: Plasmafilters
  • ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
  • 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 3826-4:2015 Plastics collapsible containers for human blood and blood components - Part 4: Aphaeresis blood bag systems with integrated features
  • ISO 3826-1:2019 Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers
  • ISO 20186-3:2019 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 3: Isolated circulating cell free DNA from plasma
  • 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 3826-2:2008 Plastics collapsible containers for human blood and blood components - Part 2: Graphical symbols for use on labels and instruction leaflets

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

  • 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 Cardiovascular implants and extracorporeal systems -Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • 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 P ISO 3826-1:2021 Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers
  • KS P ISO 7199:2012 Cardiovascular implants and artificial organs-Blood-gas exchangers(oxygenators)
  • 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 P ISO 15675:2020 Cardiovascular implants and artificial organs — Cardiopulmonary bypass systems — Arterial blood line filters
  • KS P ISO 3826-1:2019 Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers
  • 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 1135-3:2009 Transfusion equipment for medical use-Part 3:Blood-taking set
  • KS B ISO 12771-2006(2016) Plastics laboratory ware-Disposable serological pipettes
  • KS B ISO 7713-2006(2016) Laboratory glassware-Disposable serological pipettes
  • KS B ISO 12771-2006(2021) Plastics laboratory ware-Disposable serological pipettes
  • KS B ISO 7713-2006(2021) Laboratory glassware-Disposable serological pipettes
  • KS P ISO 3826-3:2019 Plastics collapsible containers for human blood and blood components — Part 3: Blood bag systems with integrated features
  • KS J ISO 8914:2007 Microbiology-General guidance for the detection of Vibrio parahaemolyticus

ES-AENOR, blood detector

Professional Standard - Medicine, blood detector

  • YY 0053-2016 Hemodialysis and related treatments Hemodialyzers, hemodiafilters, hemofilters and hemoconcentrators
  • YY 0053-2008 Cardiovascular implants and artificial organs.Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • 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 1920-2023 Dialyzer hemocompatibility test
  • YY/T 1288-2015 Nylon blood filter nets for transfusion equipments for single use
  • YY 0267-2008 Cardiovascular implants and artificial organs.Extracorporeal blood circuit for blood purification devices
  • YY/T 0456.4-2014 Reagents for hematology analyzer.Part 4:Nucleated red blood cell enumeration reagents
  • YY/T 0456.5-2014 Reagents for hematology analyzer.Part 5:Reticulocyte enumeration reagents
  • 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 0029-1990 Liquid filter for disposable blood transfusion set
  • YY/T 1156-2009 Thrombin time reagent(Kit)
  • YY 0580-2005 Cardiovascular implants and artificial organs-Cardiopulmonary bypass systems-Arterial line blood filters
  • YY 0580-2011 Cardiovascular implants and artificial organs.Cardiopulmonary bypass systems.Arterial blood line filters
  • YY 0327-2002 Human blood containers for UV rays transmission therapy for single use
  • YY/T 0142-1994 Air filter for disposable infusion and blood transfusion equipment
  • YY/T 1158-2009 Prothrombin time reagent(Kit)
  • YY 0584-2005 Blood components separation sets for single use, centrifuge bowl type
  • YY 0613-2007 Blood components separation sets for single use,centrifuge bag type
  • YY/T 0114-1993 Polyethylene special material for medical infusion, blood transfusion and syringe
  • YY 0242-1996 Polypropylene special material for medical infusion, blood transfusion and syringe
  • YY/T 0114-2008 Polyethylene material for manufacture of infusion,transfusion and injection equipments for medical use
  • YY/T 0242-2007 Polypropylene material for manufacture of infusion,transfusion and injection equipments for medical use
  • YY/T 0689-2008 Clothing for protection against contact with blood and body fluids.Determination of resistance of protective clothing materials to penetration by blood-borne pathogens.Test method using Phi-X174 bacteriophage
  • YY/T 1157-2009 Actived partial thromboplastin time reagent(Kit)

British Standards Institution (BSI), blood detector

  • 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
  • BS EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • 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
  • 16/30331650 DC BS EN 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
  • 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 ISO 3826-1:2019+A1:2023 Plastics collapsible containers for human blood and blood components - Conventional containers
  • BS EN ISO 7199:2017 Cardiovascular implants and artificial organs. Blood-gas exchangers (oxygenators)
  • BS ISO 7199:2009+A1:2012 Cardiovascular implants and artificial organs. Blood-gas exchangers (oxygenators)
  • 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 2463-1:1990 Transfusion equipment for medical use - Specification for collapsible containers for blood and blood components
  • 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 23118:2021 Tracked Changes. Molecular in vitro diagnostic examinations. Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
  • 20/30375467 DC BS EN ISO 23118. Molecular in vitro diagnostic examinations. Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
  • BS EN ISO 1135-5:2015 Tracked Changes. Transfusion equipment for medical use. Transfusion sets for single use with pressure infusion apparatus
  • 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
  • 22/30449595 DC BS EN ISO 3826-1:2019 AMD1. Plastics collapsible containers for human blood and blood components. Part 1. Conventional containers. AMENDMENT 1
  • 16/30344112 DC BS ISO/ASTM 51939. Practice for blood irradiation dosimetry
  • PD ISO/TS 23128:2019 Medical devices. Transfusion set and blood bag compatibility test method
  • BS ISO 18250-7:2018 Medical devices. Connectors for reservoir delivery systems for healthcare applications - Connectors for intravascular infusion
  • BS ISO 12771:1997 Plastics laboratory ware - Disposable serological pipettes
  • BS ISO 8637-3:2018 Extracorporeal systems for blood purification. Plasmafilters

RU-GOST R, blood detector

  • 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 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 7199-2010 Blood-gas exchangers (oxygenators). Technical requirements and test methods
  • GOST 31300-2005 Noise of machines. Liquid pumps. Noise tests
  • GOST 31209-2003 Containers for blood and its components. Requirements for chemical and biological safety and methods of testing
  • GOST R 50855-1996 Containers for blood and its components. Requirements for chemical and biological safety and methods of testing
  • GOST R 51622-2000 Polymeric containers for blood and components for single use. Technical requirements. Test methods
  • GOST 8.477-1982 State system for ensuring the uniformity of measurements. State verification schedule for liquid level measuring means
  • GOST 8.470-1982 State system for ensuring the uniformity of measurements. State verification schedule for means of measuring volume of liquid

CZ-CSN, blood detector

IN-BIS, blood detector

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

  • T/CSBT 004-2019 Quality monitoring indicators of blood testing laboratory in blood transfusion service
  • T/CSBT 007-2019 Requirements for external quality assessment of blood screening laboratory
  • T/JPMA 014-2022 Schistosoma haematobium egg detection urine filtration microscopy
  • T/CAME 38-2021 Performance validation of nucleic acid testing in blood screening
  • T/CSBME 057-2022 Adsorption resin for hemoperfusion or plasma perfusion devices
  • T/CASMES 104-2022 Enzyme-electrode biosensor blood glucose meter
  • T/CSBT 001-2019 Guideline for Haemovigilance
  • T/SHSYCXH 11-2022 Determination of free amino acids in serum—Liquid chromatography tandem mass spectrometry
  • T/NBPIA 007-2021 Classification of hemodialyzer clinical performance
  • T/CRHA 006-2022 Specification for mononuclear cell resource storage in healthy blood donors Part 3:Detection of donor blood samples
  • T/ZSA 96.6-2021 Test methods for performance parameters of dialyzer — Part 6:Performance parameters of blood compartment volume
  • T/CAMDI 006-2016 Rubber injection parts for infusion and blood transfusion equipment
  • T/CAMDI 014-2018 Air filter material for Air-inlet device in infusion sets
  • T/CSBM 0040-2023 Organ Preservation Solution containing hemoglobin-based oxygen carrier
  • T/SZAS 47-2022 Data set of genetic test for thalassemia
  • T/CAGR 001-2021 Optical Nephelometric Platelet Aggregation Assay
  • T/CSBME 043-2021 Method for measuring N-methylPyrrolidone(NMP) dissolution in hemodialyzer
  • T/CAMDI 035-2020 Disposable three-way stopcock for infusion and transfusion equipments
  • T/CAMDI 047-2020 Rigid polyvinyl chloride (PVC) special material for infusion and blood transfusion equipment
  • T/HNIMA 001-2023 Calibration method for liquid chromatograph with charged aerosol detector
  • T/CSBME 056.1-2022 Hollow fiber feedstock for hemodialyzers Part 1: Polysulfone
  • T/CAMDI 002-2016 TOTM plasticized polyvinyl chloride (PVC) special material for infusion and blood transfusion equipment
  • T/SHSYCXH 9-2022 Detection method for sarcosine in serum samples - Enzyme coupled colorimetric assay

未注明发布机构, blood detector

  • 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
  • BS EN ISO 3826-1:2019 Plastics collapsible containers for human blood and blood components Part 1 : Conventional containers
  • BS 6706:1986(2011) Specification for Disposable glass serological pipettes
  • BS ISO 12771:1997(1999) Plastics Laboratory Ware — Disposable serological pipettes
  • BS EN ISO 3826-3:2007(2008) Plastics collapsible containers for human blood and blood components — Part 3 : Blood bag systems with integrated features
  • BS EN ISO 1135-4:2015(2016) Transfusion equipment for medical use Part 4 : Transfusion sets for single use, gravity feed
  • JIS T 3232:2023 Blood filters for cardiopulmonary bypass systems

Danish Standards Foundation, blood detector

  • DS/EN 1283:1997 Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
  • DS/EN ISO 8637-1:2021 Extracorporeal systems for blood purification – Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • DS/EN ISO 3826-1:2013 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers
  • 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/ISO 23118:2021 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
  • DS/EN ISO 3826-3:2008 Plastics collapsible containers for human blood and blood components - Part 3: Blood bag systems with integrated features
  • DS/ISO 1135-3:1993 Transfusion equipment for medical use. Part 3 : Blood-taking sets
  • DS/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

Lithuanian Standards Office , blood detector

  • LST EN 1283-2001 Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
  • LST EN ISO 3826-1:2004 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2003)
  • LST EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)
  • 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)

Association Francaise de Normalisation, blood detector

  • NF EN ISO 8637-1:2020 Systèmes extracorporels pour la purification du sang - Partie 1 : hémodialyseurs, hémodiafiltres, hémofiltres et hémoconcentrateurs
  • 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 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 S93-302-2*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 S93-230-1:2013 Plastics collapsible containers for human blood and blood components - Part 1: conventional containers
  • 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 7199:2017 Implants cardiovasculaires et organes artificiels - Échangeurs gaz/sang extracorporels (oxygénateurs)
  • NF S62-084*NF EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
  • 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 U47-210:2016 Animal health analysis methods - Isolation of hemagglutinating avian myxoviruses by ovoculture and detection of their hemagglutinating activity
  • NF EN ISO 7199/A1:2020 Implants cardiovasculaires et organes artificiels - Échangeurs gaz/sang extracorporels (oxygénateurs) - Amendement 1 : raccords
  • NF S90-304:1989 MEDICO-SURGICAL EQUIPMENT. HAEMODIALYSIS EQUIPMENT. OPERATING DATA.
  • NF EN ISO 23118:2021 Analyses de diagnostic moléculaire in vitro - Spécifications relatives aux processus préanalytiques pour l'analyse du métabolome dans l'urine et le sang veineux (sérum et plasma)
  • NF U47-012:2001 Animal health analysis method - Detection of specific antibodies of Mycoplasma gallisepticum, Mycoplasma meleagridis or Mycoplasma synoviae in serum by the Rapid Serum Agglutination Test.
  • NF U47-012:2009 Animal health analysis method - Detection of specific antibodies of Mycoplasma gallisepticum, Mycoplasma meleagridis or Mycoplasma synoviae in serum bu the Rapid Serum Agglutination Test
  • NF S93-230-2*NF 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

German Institute for Standardization, blood detector

  • 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 12750:1969-02 Blood dilution pipettes for blood corpuscles counting
  • DIN 58931:1995 Haematology - Determination of haemoglobin concentration in blood - Reference method
  • 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 EN 12022:1999 Blood gas exchangers; German version EN 12022:1999
  • 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 8637:2014 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 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 58932-3:1994 Haematology; determination of the concentration of blood corpuscles in blood; determination of the concentration of erythrocytes; reference method
  • 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 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 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 58932-1:2023-08 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 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 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 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 58932-3:2017 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 58931:2010 Haematology - Determination of haemoglobin concentration in blood - Reference method; Text in German and English
  • 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 12845:1972 Westergren tubes for the erythrocyte sedimentation rate of red blood corpuscles
  • 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 23118:2021-08 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021); German version EN ISO 23118:2021
  • DIN 58935-1:1997 Haematologie - Determination of the erythrocyte sedimentation rate in blood - Part 1: Selected method
  • 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 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 ISO 1135-5:2016-06 Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus (ISO 1135-5:2015); German version EN ISO 1135-5:2015
  • 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 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 58914-1:2000-03 Haemostaseology - Determination of thrombin time - Part 1: Reference measurement procedure for the determination in plasma from citrated venous blood
  • 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 23118:2020 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO/DIS 23118:2020); German and English version prEN ISO 23118:2020
  • 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 58910-2:2000-03 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 2: Reference measurement procedure for the determination in citrated venous blood
  • 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 EN ISO 1135-4:2016-06 Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed (ISO 1135-4:2015); German version EN ISO 1135-4:2015
  • DIN 58910-4:2000 Haemostaseology - Determination of thromboplastin (prothrombin) time - Part 4: Reference measurement procedure for the determination in capillary blood
  • DIN 58911-1:2000-03 Haemostaseology - Calibration of measurement procedures - Part 1: Clotting time measurement procedures
  • 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 58908:2015-09 Haemostaseology - Determination of activated partial thromboplastin time (APTT) - Reference measurement procedure; Text in German and English
  • 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 EN ISO 3826-1:2013 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2013); German version EN ISO 3826-1:2013
  • 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 ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021); German version EN ISO 23118:2021
  • DIN 58910-3:2000 Haemostaseology - Determination of the thromboplastin (prothrombin) time - Part 3: Reference measurement procedure for the determination in citrated capillary blood
  • DIN 51614:1989-12 Testing of liquefied petroleum gases; detection of ammonia, water and alkaline solution
  • 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 7199:2017 Cardiovascular implants and artificial organs - Blood-gas exchangers (oxygenators) (ISO 7199:2016); German version EN ISO 7199:2017
  • DIN 58909-1:2020 Haemostaseology - Determination of factor VIII coagulant activity (FVIII:C) - Part 1: Reference measurement procedure for the one-stage method; Text in German and English
  • DIN 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 (ISO 3826-2:2008); English version of DIN EN ISO 3826-2:2008-11
  • DIN EN ISO 1135-4:2023-11 Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed (ISO/DIS 1135-4:2023); German and English version prEN ISO 1135-4:2023 / Note: Date of issue 2023-09-29*Intended as replacement for DIN EN ISO 1135-4 (2016-06).
  • DIN 58909-1:2020-04 Haemostaseology - Determination of factor VIII coagulant activity (FVIII:C) - Part 1: Reference measurement procedure for the one-stage method; Text in German and English
  • DIN EN ISO 23908:2023-11 Sharps injury protection - Requirements and test methods - Sharps protection mechanisms for single-use needles, introducers for catheters and needles used for blood testing, monitoring, sampling and medical substance administration (ISO/DIS 23908:2023)...
  • DIN EN ISO 1135-5:2023-11 Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus (ISO/DIS 1135-5:2023); German and English version prEN ISO 1135-5:2023 / Note: Date of issue 2023-09-29*Intended as replacement for DIN EN ...
  • DIN 58911-2:2000-03 Haemostaseology - Calibration of measurement procedures - Part 2: Photometric measurement procedures

ES-UNE, blood detector

  • 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 ISO 3826-1:2020 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2019)
  • UNE-EN ISO 23118:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)
  • 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 1135-4:2016 Transfusion equipment for medical use - Part 4: Transfusion sets for single use, gravity feed (ISO 1135-4:2015)
  • UNE-EN ISO 1135-5:2016 Transfusion equipment for medical use - Part 5: Transfusion sets for single use with pressure infusion apparatus (ISO 1135-5:2015)

Canadian Standards Association (CSA), blood detector

  • 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)
  • 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 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 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)

US-AAMI, blood detector

  • 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

AT-ON, blood detector

  • ONORM EN 1283-1996 Haemodialysers,haemodiafilters,haemofilters,haemoconcentrators and their extracorporeal circuits
  • OENORM EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)
  • ONORM K 2030-1983 Refrigerators for blood conservation; definitions, requirements, fest

Professional Standard - Public Safety Standards, blood detector

  • GA 656-2006 Detection method for ABO blood type in human blood(stains). Hemagglutination test, elution test
  • GA 657-2006 Detection method for ABO blood type in human body fluid stains. Hemagglutination inhibition test
  • GA/T 842-2019 Examination methods for ethanol concentration in blood
  • GA/T 842-2009 How to test blood alcohol content
  • GA/T 2073-2023 Forensic sciences—Examination methods for carboxyhaemoglobin in blood samples—Spectrophotometry
  • GA/T 1632-2019 Liquid chromatography-mass spectrometry for the detection of metramine and chlormequat in forensic science blood and urine
  • GA/T 1320-2016 GC-MS examination methods for fluoride ion in urine and blood in forensic science
  • GA 655-2006 Detection method for ABO blood type in human hairs. Elution test
  • GA/T 1331-2016 LC-MS/MS examination methods for abamectin Bla in blood samples in forensic science
  • GA/T 1147-2014 Labortory specifications for examination of ethanol concentration in driver's blood
  • GA 765-2008 Detection method of human hemoglobin.Rapid test strip
  • GA/T 765-2020 Human hemoglobin detection gold standard reagent strip method
  • GA/T 1629-2019 Paraquat detection in blood and urine for forensic science by gas chromatography and gas chromatography-mass spectrometry
  • GA/T 204-2019 Headspace Gas Chromatography for the Detection of Benzene, Toluene, Ethylbenzene and Xylene in Blood and Urine for Forensic Science
  • GA/T 1630-2019 Inductively Coupled Plasma Mass Spectrometry for Forensic Science Blood and Urine Tests for Five Elements including Chromium
  • GA/T 1633-2019 Forensic Science Blood, Urine Ethyl Glucuronide Detection Gas Chromatography-Mass Spectrometry and Liquid Chromatography-Mass Spectrometry

SE-SIS, blood detector

KR-KS, blood detector

  • 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 P ISO 3826-1-2021 Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers
  • 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 8637-3-2022 Extracorporeal systems for blood purification Part 3: Plasmafilters
  • 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 15675-2020 Cardiovascular implants and artificial organs — Cardiopulmonary bypass systems — Arterial blood line filters
  • KS P ISO 3826-1-2019 Plastics collapsible containers for human blood and blood components — Part 1: Conventional containers
  • KS P ISO 3826-3-2019 Plastics collapsible containers for human blood and blood components — Part 3: Blood bag systems with integrated features
  • KS J ISO 8914-2007 Microbiology-General guidance for the detection of Vibrio parahaemolyticus

CEN - European Committee for Standardization, blood detector

  • EN ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers@ haemodiafilters and haemofilters

Indonesia Standards, blood detector

  • SNI ISO 8638:2012 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

American National Standards Institute (ANSI), blood detector

RO-ASRO, blood detector

  • STAS 11326/4-1984 RUBBER STOPPERS FOR RECIPIENTS OF BLOOD, PLASMA AND AQUEOUS SOLUTIONS FOR INJECTIONS AND PERFUSIONS Hcmolityc impurities checking up
  • 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 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 11327/2-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Apparence, smell and taste checking out
  • STAS 11327/9-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Organic substances determination
  • STAS 11327/8-1983 RUBBER STOPPERS FOR BLOOD,PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS etermination of volatile sulphides
  • STAS 7352/1-1988 APPARATUS FOR BLOOD PRESSURE MEASUREMENT WITH MERCURY GAUGES General technical requirements for quality
  • 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
  • STAS 11327/7-1983 RUBBER STOPPERS FOR BLOOD, LASMA AND SOLUTION BOTTLES OR INJECTIONS AND PERFUSI- NS etermination of residue at evaporation of aqueous extract
  • STAS 11326/7-1989 RUBBER STOPPERS FOR PARENTHERAL USE BLOOD AND PREPARATOION BOTTLES Microbiological proofing checking up
  • STAS 11327/6-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Determination of ammonium, chlor and sulphate ions of aqueous extract

AENOR, blood detector

  • 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 81594:1992 BIOLOGICAL CONTROL. DETERMINATIO OF ZINC PROTOPORPHYRIN (ZPP) IN BLOOD. METHOD OF DIRECT READING (HEMATOFLUOROMETER).
  • UNE-EN ISO 3826-1:2013 Plastics collapsible containers for human blood and blood components - Part 1: Conventional containers (ISO 3826-1:2013)
  • 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)

Professional Standard - Commodity Inspection, blood detector

  • 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 0967-2000 Rules for the inspection of once using infusion and transfusion sets for import and export
  • SN/T 4352-2015 Inspection and quarantine procedure for feeding blood products
  • SN/T 0323.1-2007 Rules for the inspection of medical equipment for import and export.Part 1:Infusion and transfusion sets for single use
  • SN/T 1498-2004 Determination of magnesium L-ascorbyl-2-phosphate in cosmetics-Liquid chromatography
  • SN/T 2121-2014 Quarantine protocol for epizootic haematopoietic necrosis
  • SN/T 1139-2002 Serological detection method of faba bean staining virus
  • SN/T 1224-2003 Rapid Serum Agglutination Test for Antibody Detection of Mycoplasma Gallisepticum Infection
  • SN/T 2121-2008 Protocol of quarantine for epizootic haematopoietic necrosis
  • SN/T 1474-2015 Technical specifications for quarantine of infectious hematopoietic organ necrosis
  • SN/T 1612-2005 Serological detection method of carnation ringspot dianthovirus
  • SN/T 1611-2005 Serological detection method of southern bean mosaic sobemovirus
  • SN/T 1611-2013 Serological detection methods of Southern bean mosaic virus

国家药监局, blood detector

  • 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 0464-2019 Disposable hemoperfusion device
  • YY/T 1856-2023 General safety requirements for blood, intravenous solution, and lavage fluid warmers
  • YY/T 1658-2019 Method for determination of cyclohexanone dissolution in infusion and blood transfusion equipment
  • YY/T 1628-2019 Polyvinyl chloride granules for medical infusion and blood transfusion equipment

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

  • JJF 1541-2015 Calibration Specification for Hemodialysis Equipment Tester

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

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

TH-TISI, blood detector

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

Military Standards (MIL-STD), blood detector

VN-TCVN, blood detector

  • TCVN 7611-2007 Plastics collapsible containers for human blood and blood components

Professional Standard - Machinery, blood detector

Professional Standard - Agriculture, blood detector

  • 236药典 四部-2015 3300 Microbiological Inspection Method 3306 Technical Requirements for Human Plasma Virus Nucleic Acid Detection for Production of Blood Products
  • 227药典 四部-2020 3300 Microbiological Inspection Method 3306 Technical Requirements for Human Plasma Virus Nucleic Acid Detection for Production of Blood Products
  • 255药典 三部-2015 Microbiological Examination Method 3306 General Rules for the Technical Requirements for Human Plasma Virus Nucleic Acid Detection in the Production of Blood Products 103
  • 278药典 三部-2020 Microbiological Examination Method 3306 General Rules for the Technical Requirements for Human Plasma Virus Nucleic Acid Detection in the Production of Blood Products 103
  • 4 OIE陆生动物诊断试验和疫苗手册-2005 r-interferon test for bovine tuberculosis hematological examination
  • NY/T 2417-2013 Polymerase chain reaction (PCR) for detection of Haemophilus parasuis
  • GB/T 42430-2023 Examination of ethanol, methanol, n-propanol, acetone, isopropanol and n-butanol in blood and urine
  • 农业部公告第1834号 New veterinary drugs: 1. Avian Leukosis Virus ELISA Antigen Detection Kit; 2. Ginseng Leaf Oral Liquid
  • 314药典 四部-2020 4000 Testing method for drug packaging material 4013 Hemolysis test method for drug packaging material
  • 284药典 三部-2010 Appendix ⅩⅢ ⅩⅢD Newborn bovine serum testing requirements
  • 302药典 三部-2020 Bioassay 3422 Human thrombin activity assay
  • 241药典 三部-2020 Content Determination Method 3120 Determination of Sugar and Sugar Alcohol in Human Blood Products

国家食品药品监督管理局, blood detector

  • YY/T 1556-2017 Methods for testing particulate contamination of medical infusion, blood transfusion, and injection equipment
  • YY/T 1551.2-2017 Air filters for infusion and blood transfusion equipment - Part 2: Test methods for bacterial retention in liquids
  • YY/T 1422-2016 Serum pregnancy-related plasma protein A detection reagent (box) (quantitative labeling immunoassay)

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

  • 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 36194-2018 Detection method of goldfish haematopoietic necrosis virus
  • GB 14232.3-2011 Plastics collapsible containers for human blood and blood components. Part 3:Blood bag systems with integrated features
  • GB/T 14233.2-1993 Test methods for infusion, blood transfusion and syringes for medical devices - Part 2: Bioanalytical methods
  • GB/T 14233.1-1998 Infusion, transfusion, injection equipment for medical use--Part 1: Chemical analysis methods
  • GB/T 14233.1-2008 Test methods for infusion,transfusion,injection equipments for medical use.Part 1:Chemical analysis methods
  • GB/T 14233.1-2022 Test methods for infusion, transfusion, injection equipments for medical use—Part 1: Chemical analysis methods
  • GB 15593-1995 Plasticized polyvinyl chloride (PVC) compounds for transfusion (infusion) equipment
  • GB/T 14233.2-2005 Test methods for infusion,transfusion,injection equipment for medical use.Part 2:Biological test methods
  • GB/T 26426-2010 Method for determination of Vibrio paraheamolyticus in feeds
  • GB 19522-2004 Blood-breath alcohol concentration and examination for driving
  • GB 19522-2010 Blood & breath alcohol concentration and examination for vehicle drivers
  • GB/T 14232.2-2015 Bag plastic containers for human blood and blood components - Part 2: Graphical symbols for labeling and instructions for use
  • GB/T 14926.21-2008 Laboratory animal.Method for examination of Rabbit hemorrhagic disease virus(RHDV)
  • GB/T 14926.21-2001 Laboratory animal--Method for examination of rabbit hemorrhagic disease virus(RHDV)

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

  • 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
  • GB/T 15593-2020 Plasticized poly(vinyl chloride) compounds for transfusion (infusion) equipment
  • GB/T 36873-2018 Code of practice for detection of avian leukosis infection in chicken pedigree breeder flock

未注明发布机构, blood detector

  • 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
  • BS EN ISO 3826-1:2019 Plastics collapsible containers for human blood and blood components Part 1 : Conventional containers
  • BS 6706:1986(2011) Specification for Disposable glass serological pipettes
  • BS ISO 12771:1997(1999) Plastics Laboratory Ware — Disposable serological pipettes
  • BS EN ISO 3826-3:2007(2008) Plastics collapsible containers for human blood and blood components — Part 3 : Blood bag systems with integrated features
  • BS EN ISO 1135-4:2015(2016) Transfusion equipment for medical use Part 4 : Transfusion sets for single use, gravity feed
  • JIS T 3232:2023 Blood filters for cardiopulmonary bypass systems

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

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

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

  • JJG 553-1988 Verification Regulation of Blood Gas Acid-Base Analyser
  • JJG 646-2006 Verification Regulation of Locomotive Pipette
  • JJG 692-2010 Verification Regulation of Non-invasive Automated Sphygmomanometers

中华人民共和国国家卫生和计划生育委员会, blood detector

  • 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

国家卫生计生委, blood detector

卫生健康委员会, blood detector

Professional Standard - Hygiene , blood detector

  • WS/T 461-2015 Measurement of Hemoglobin A<下标1c>
  • WS/T 225-2002 Collection and processing of blood specimens for clinical chemistry
  • WS/T 406-2012 Analytical quality specifications for routine tests in clinical hematology
  • WS/T 463-2015 Measurement of serum low density lipoprotein cholesterol
  • WS/T 478-2015 Operating guidelines for measurement of serum 25-hydroxyvitamin D<下标3>.Isotope dilution liquid chromatography tandem mass spectrometry

International Electrotechnical Commission (IEC), blood detector

  • 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

Liaoning Provincial Standard of the People's Republic of China, blood detector

  • DB21/T 2619-2016 Infectious hematopoietic organ necrosis virus LAMP detection method

IT-UNI, blood detector

  • UNI EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
  • UNI ISO 18250-7:2021 Medical devices -- Connectors for reservoir delivery systems for healthcare applications - Part 7: Connectors for intravascular infusion

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

  • ASTM F2172-02 Standard Specification for Blood/Intravenous Fluid/Irrigation Fluid Warmers
  • ASTM ISO/ASTM51939-17(2022) Standard Practice for Blood Irradiation Dosimetry
  • ASTM E1303-95(2005) Practice for Refractive Index Detectors Used in Liquid Chromatography
  • ASTM F2888-19 Standard Practice for Platelet Leukocyte Count—An In-Vitro Measure for Hemocompatibility Assessment of Cardiovascular Materials
  • ASTM E1303-95 Practice for Refractive Index Detectors Used in Liquid Chromatography
  • ASTM E1303-95(2000) Practice for Refractive Index Detectors Used in Liquid Chromatography

BR-ABNT, blood detector

Tianjin Provincial Standard of the People's Republic of China, blood detector

  • DB12/ 402-2008 Estimation and Inspection of Blood Alcohol Content of Vehicle Personnel
  • DB12/T 749-2017 General specification for centralized testing of blood stations

CU-NC, blood detector

Professional Standard - Ocean, blood detector

  • HY/T 151-2013 Detection of hemolytic toxins in marine microalgae.Erythrocyte lysis assay

CH-SNV, blood detector

  • SN EN ISO 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma (ISO 23118:2021)

国家技术监督局, blood detector

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

中华人民共和国国家质量监督检验检疫总局、中国国家标准化管理委员会, blood detector

其他未分类, blood detector

  • BJY 201805 Supplementary test method for inspection items of cowhide-derived ingredients in Ejiao Buxue Oral Liquid

司法部, blood detector

  • SF/T 0115-2021 Liquid chromatography-tandem mass spectrometry detection method for 45 toxic alkaloids in blood
  • SF/T 0092-2021 Liquid chromatography-tandem mass spectrometry method for detecting 20 herbicides including prometryn in blood
  • SF/T 0113-2021 Gas chromatography-mass spectrometry and gas chromatography test methods for cyanide in blood
  • SF/T 0064-2020 Gas chromatography-high-resolution mass spectrometry detection method for 188 poisons (drugs) in blood

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

国家质量监督检验检疫总局, blood detector

  • SN/T 4820-2017 PCR-DHPLC detection method for bovine citrullinemia
  • SN/T 1474-2014 Technical specifications for quarantine of infectious hematopoietic necrosis disease

国家医药管理局, blood detector

  • YY 0114-1993 Special polyethylene materials for medical infusion, blood transfusion and syringes

海关总署, blood detector

  • SN/T 5181-2020 Technical specifications for quarantine of goldfish hematopoietic organ necrosis disease

HU-MSZT, blood detector

Ningxia Provincial Standard of the People's Republic of China, blood detector

  • DB64/T 1008-2014 Main Blood Biochemical Indexes and Determination Methods of Tan Sheep

Inner Mongolia Provincial Standard of the People's Republic of China, blood detector

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

Agricultural Standard of the People's Republic of China, blood detector

Shandong Provincial Standard of the People's Republic of China, blood detector

  • DB37/T 2995-2017 Fluorescent quantitative PCR detection technique for Haemophilus parasuis

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

  • DB32/T 2599-2013 Detection of Enterohaemorrhagic Escherichia coli O157:H7 in Livestock and Poultry
  • DB32/T 3762.15-2021 Technical Specifications for Detection of Novel Coronavirus Part 15: Procedures for Detection of Serum/Plasma IgM and IgG Antibody Magnetic Particle Chemiluminescent Method

农业农村部, blood detector

  • NY/T 2960-2016 Rabbit viral hemorrhagic disease virus RT-PCR detection method




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