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In Vitro Blood Tests

In Vitro Blood Tests, Total:462 items.

In the international standard classification, In Vitro Blood Tests involves: Medical equipment, Laboratory medicine, Veterinary medicine, Protection against crime, Biology. Botany. Zoology, Quality, Medical sciences and health care facilities in general, Protective equipment, Farming and forestry, Precision mechanics, Occupational safety. Industrial hygiene, Valves, Measurement of volume, mass, density, viscosity, Paints and varnishes, Testing of metals, Iron and steel products, Shipbuilding and marine structures in general, Non-destructive testing, Acoustics and acoustic measurements, Rubber, Fluid storage devices, General methods of tests and analysis for food products, Water quality, Fuels, Animal feeding stuffs, Radiation protection, Vocabularies, Fluid power systems, Fertilizers, Soil quality. Pedology, Analytical chemistry, Petroleum products in general, Thermodynamics and temperature measurements, Equipment for petroleum and natural gas industries, Pipeline components and pipelines, Beekeeping, Fruits. Vegetables, Beverages, Prepackaged and prepared foods, Products of the chemical industry, Lubricants, industrial oils and related products, Petroleum, petroleum products and natural gas handling equipment, Electrical equipment for working in special conditions, Environmental testing.

International Organization for Standardization (ISO), In Vitro Blood Tests

ISO/FDIS 8637-2:2023 Extracorporeal systems for blood purification — Part 2: Extracorporeal blood and fluid circuits for haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
ISO 8638:2010 Cardiovascular implants and extracorporeal systems - 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 8638:1989 Extracorporeal blood circuit for haemodialysers, haemofilters and haemoconcentrators
ISO/DIS 8637-2 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 8637:2010 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 23118:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
ISO 8638:2004 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
ISO 18242:2016 Cardiovascular implants and extracorporeal systems - Centrifugal blood pumps
ISO 8637-3:2018 Extracorporeal systems for blood purification - Part 3: Plasmafilters
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 11658:2012 Cardiovascular implants and extracorporeal systems - Blood/tissue contact surface modifications for extracorporeal perfusion systems
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 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 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood
ISO/DIS 8637-3 Extracorporeal systems for blood purification — Part 3: Plasmafilters
ISO/CD 8637-3 Extracorporeal systems for blood purification — Part 3: Plasmafilters
ISO 4987:2010 Steel castings - Liquid penetrant inspection
ISO 4987:2020 Steel and iron castings — Liquid penetrant testing
ISO 18242:2016/DAmd 1 Cardiovascular implants and extracorporeal systems — Centrifugal blood pumps — Amendment 1: Worst-case conditions for testing
ISO 16604:2004 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-X 174 bacteriophage
ISO 20186-1:2019 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA
ISO 17593:2007 Clinical laboratory testing and in vitro medical devices - Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
ISO 20186-2:2019 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 2: Isolated genomic DNA
ISO 18242:2016/Amd 1:2011 Cardiovascular implants and extracorporeal systems — Centrifugal blood pumps — Amendment 1: Worst-case conditions for testing
ISO 18242:2016/FDAmd 1 Cardiovascular implants and extracorporeal systems — Centrifugal blood pumps — Amendment 1: Worst-case conditions for testing
ISO 9583:1993 Implants for surgery; non-destructive testing; liquid penetrant inspection of metallic surgical implants
ISO 4307:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA
ISO 3453:1984 Non-destructive testing; Liquid penetrant inspection; Means of verification
ISO 11755:1996 Cylinders in bundles for permanent and liquefiable gases (excluding acetylene) - Inspection at time of filling
ISO/TS 23810:2006 Cardiovascular implants and artificial organs - Checklist for preoperative extracorporeal circulation equipment setup
ISO/TS 23810:2012 Cardiovascular implants and artificial organs - Checklist for preoperative extracorporeal circulation equipment setup
ISO/TS 23810:2018 Cardiovascular implants and artificial organs - Checklists for use of extracorporeal circulation equipment
ISO 24431:2006 Gas cylinders - Cylinders for compressed and liquefied gases (excluding acetylene) - Inspection at time of filling
ISO 20179:2005 Water quality - Determination of microcystins - Method using solid phase extraction (SPE) and high performance liquid chromatography (HPLC) with ultraviolet (UV) detection
ISO 11755:2005 Gas cylinders - Cylinder bundles for compressed and liquefied gases (excluding acetylene) - Inspection at time of filling
ISO 15197:2013 In vitro diagnostic test systems.Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
ISO 15197:2003 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
ISO 2812-1:2007 Paints and varnishes - Determination of resistance to liquids - Part 1: Immersion in liquids other than water
ISO 2812-1:2017 Paints and varnishes - Determination of resistance to liquids - Part 1: Immersion in liquids other than water
ISO 11369:1997 Water quality - Determination of selected plant treatment agents - Method using high performance liquid chromatography with UV detection after solid-liquid extraction
ISO/TS 17822-1:2014 In vitro diagnostic test systems - Qualitative nucleic acid-based in vitro examination procedures for detection and identification of microbial pathogens - Part 1: General requirements, terms and definitions

Japanese Industrial Standards Committee (JISC), In Vitro Blood Tests

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 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 8061:2007 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
JIS T 8061:2010 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
JIS T 8061:2015 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
JIS T 0403:2018 Method for in vitro thrombogenicity testing for inflow cannula of left ventricular assist system

Korean Agency for Technology and Standards (KATS), In Vitro Blood Tests

KS P ISO 8638-2012(2017) Cardiovascular implants and extracorporeal systems －Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
KS P ISO 8638:2012 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 6123-2006 Electric motor driven blood pump for cardiopulmonary bypass
KS P ISO 9583-2009(2019) Implants for surgery－Non-destructive testing－Liquid penetrant inspection of metallic surgical implants
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 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 B 50117-2005(2020) Measuring systems for liquids other than water
KS K ISO 16604-2012(2022) 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 bacte
KS K ISO 16604:2012 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
KS P ISO 17593:2009 Clinical laboratory testing and in vitro medical devices－Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
KS B ISO 3453-2006(2011) Non－destructive testing－Liquid penetrant inspection－Means of verification
KS P ISO TS 23810:2009 Cardiovascular implants and artificial organs－Checklist for preoperative extracorporeal circulation equipment setup
KS P ISO 16256:2017 Clinical laboratory testing and in vitro diagnostic test systems ─ Reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases
KS P ISO 9583:2009 Implants for surgery-Non-destructive testing-Liquid penetrant inspection of metallic surgical implants
KS K ISO 16604-2012(2017) 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 bacte
KS B ISO 11755:2005 Cylinders in bundles for permanent and liquefiable gases(excluding acetylene)-Inspection at time of filling
KS B ISO 11755:2013 Cylinders in bundles for permanent and liquefiable gases(excluding acetylene)－Inspection at time of filling
KS M ISO 2812-1-2012(2017) Paints and varnishes－Determination of resistance to liquids－ Part 1：Immersion in liquids other than water
KS M ISO 2812-1:2022 Paints and varnishes — Determination of resistance to liquids — Part 1: Immersion in liquids other than water
KS B 0816-1993 Method for liquid penetrant testing and classification of the indication
KS B 0816-1987 Method for liquid penetrant testing and classification of the indication
KS P ISO 15197:2010 In vitro diagnostic test systems－Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
KS P ISO 15197:2017 In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
KS I ISO 11264-2016(2021) Soil quality－Determination of herbicides－Method using HPLC with UV-detection
KS B 50117-2005 Measuring systems for liquids other than water
KS M 1920-2002 Liquid halogenated hydrocarbons for industrial use-Determination of acidity-Titrimetric method
KS B 5314-1986(2016) Liquid-in-glass thermometers for testing of petroleum products
KS I ISO 11369:2008 Water quality－Determination of selected plant treatment agents－Method using high performance liquid chromatography with UV detection after solid-liquid extraction
KS B OIMLR 120-2006(2016) Standard capacity measures for testing measuring systems for liquids other than water
KS I ISO 11369-2008(2018) Water quality－Determination of selected plant treatment agents－Method using high performance liquid chromatography with UV detection after solid-liquid extraction
KS B 0816-2021 Method for liquid penetrant testing and classification of the penetrant indication
KS D ISO 12095-2002(2017) Seamless and welded steel tubes for pressure purposes－Liquid penetrant testing

ES-UNE, In Vitro Blood Tests

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 8637-1:2020 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
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 6717:2022 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)
UNE-CEN/TS 17742:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma (Endorsed by Asociación Española de Normalización in May of 2022.)
UNE-CEN/TS 17747:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins (Endorsed by Asociación Española de Normalización in June of 2022.)
UNE-EN ISO 20186-3:2020 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)
UNE-EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA (ISO 20186-1:2019)
UNE-EN ISO 20186-2:2020 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO 20186-2:2019)
UNE-EN ISO 4307:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA (ISO 4307:2021)
UNE-EN ISO 2812-1:2018 Paints and varnishes - Determination of resistance to liquids - Part 1: Immersion in liquids other than water (ISO 2812-1:2017)
UNE-EN ISO 15197:2015 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)

Association Francaise de Normalisation, In Vitro Blood Tests

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 EN ISO 8637-1:2020 Systèmes extracorporels pour la purification du sang - Partie 1 : hémodialyseurs, hémodiafiltres, hémofiltres et hémoconcentrateurs
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 S93-302*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 S93-308:1992 EXTRACORPORAL CIRCUITS. IDENTIFICATION OF CONCENTRATE SOLUTIONS FOR HEMODIALYSIS.
NF EN ISO 7199:2017 Implants cardiovasculaires et organes artificiels - Échangeurs gaz/sang extracorporels (oxygénateurs)
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 EN ISO 7199/A1:2020 Implants cardiovasculaires et organes artificiels - Échangeurs gaz/sang extracorporels (oxygénateurs) - Amendement 1 : raccords
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 S92-036:2004 In vitro diagnostic medical devices - Single-use receptables for the collection of specimens, other than blood, from humans.
NF S92-036*NF EN ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood
NF S92-075-3*NF 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
NF EN ISO 6717:2021 Dispositifs médicaux de diagnostic in vitro - Récipients à usage unique pour le prélèvement d'échantillons d'origine humaine autres que le sang
NF S92-075-1*NF EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1 : isolated cellular RNA
XP S92-075-1*XP CEN/TS 16835-1:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1 : isolated cellular RNA
NF S92-075-2*NF EN ISO 20186-2:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2 : isolated genomic DNA
XP S92-075-2*XP CEN/TS 16835-2:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2 : isolated genomic DNA
NF S92-076*NF EN ISO 4307:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA
NF EN 15856:2010 Essais non destructifs - Émission acoustique - Principes généraux des contrôles par émission acoustique pour la détection de la corrosion dans une enceinte métallique remplie de liquide
NF U47-210:2016 Animal health analysis methods - Isolation of hemagglutinating avian myxoviruses by ovoculture and detection of their hemagglutinating activity
NF EN 13365:2002 Bouteilles à gaz transportables - Cadres de bouteilles pour gaz permanents et liquéfiés (sauf l'acétylène) - Inspection au moment du remplissage
NF EN 13365/A1:2005 Bouteilles à gaz transportables - Cadres de bouteilles pour gaz permanents et liquéfiés (sauf l'acétylène) - Inspection au moment du remplissage
NF E29-782:2000 Transportable gas cylinders - Cylinders for liquified gases (excluding actylene and L.P.G.) - Inspection at time of filling.
NF EN ISO 11755:2020 Bouteilles à gaz - Cadres de bouteilles pour gaz comprimés et liquéfiés (à l'exclusion de l'acétylène) - Inspection au moment du remplissage
NF S92-026*NF EN ISO 15197:2015 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
NF T30-053-1:2007 Paints and varnishes - Determination of resistance to liquids - Part 1 : immersion in liquids other than water.
NF T30-053-1*NF EN ISO 2812-1:2017 Paints and varnishes - Determination of resistance to liquids - Part 1 : immersion in liquids other than water
NF EN ISO 2812-1:2017 Peintures et vernis - Détermination de la résistance aux liquides - Partie 1 : immersion dans des liquides autres que l'eau
NF S92-026:2004 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus.
NF S92-026:2013 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
NF EN ISO 20186-3:2019 Analyses de diagnostic moléculaire in vitro - Spécifications relatives aux processus préanalytiques pour le sang total veineux - Partie 3 : ADN libre circulant extrait du plasma
NF EN 238/A1:2005 Produits pétroliers liquides - Essence - Détermination de la teneur en benzène par spectrométrie infrarouge
NF EN 238:1996 Produits pétroliers liquides - Essence - Détermination de la teneur en benzène par spectrométrie infrarouge.
NF ISO 11264:2008 Qualité du sol - Dosage des herbicides - Méthode par CLHP avec détection par UV

German Institute for Standardization, In Vitro Blood Tests

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 8637-1:2020-10 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 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 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 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 ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
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 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 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 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans; German version EN 14254:2004
DIN CEN/TS 17742:2022-07 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma; German version CEN/TS 17742:2022
DIN CEN/TS 17747:2022-08 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins; German version CEN/TS 17747:2022
DIN EN ISO 6717:2020 In vitro diagnostic medical devices - Single-use containers for the collection of specimens, other than blood, from humans (ISO/DIS 6717:2020); German and English version prEN ISO 6717:2020
DIN EN ISO 6717:2021-12 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021); German version EN ISO 6717:2021
DIN EN ISO 20186-3:2020-04 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); German version EN ISO 20186-3:2019
DIN CEN/TS 17811:2022-08 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNA; German version CEN/TS 17811:2022
DIN EN ISO 20186-3:2020 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)
DIN EN ISO 20186-1:2019-08 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA (ISO 20186-1:2019); German version EN ISO 20186-1:2019
DIN EN ISO 20186-2:2019-08 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO 20186-2:2019); German version EN ISO 20186-2:2019
DIN 58933-1:1995-01 Haematology - Procedure for determining the volume fraction of erythrocytes (packed cell volume) in blood - Part 1: Reference method based on centrifugation
DIN EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA (ISO 20186-1:2019)
DIN EN ISO 20186-2:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA (ISO 20186-2:2019)
DIN CEN/TS 17390-2:2020-05 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 2: Isolated DNA; German version CEN/TS 17390-2:2020
DIN CEN/TS 17390-1:2020-05 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNA; German version CEN/TS 17390-1:2020
DIN EN ISO 4307:2022-02 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA (ISO 4307:2021); German version EN ISO 4307:2021
DIN EN ISO 2812-1:2018-03 Paints and varnishes - Determination of resistance to liquids - Part 1: Immersion in liquids other than water (ISO 2812-1:2017); German version EN ISO 2812-1:2017
DIN 51762:1974 Testing of Liquid Fuels; Determination of Reaction to Sulphuric Acid
DIN 51798:2018 Testing of liquid fuels - Determination of the crystallization point of pure benzene
DIN 51798:2005 Testing of liquid fuels - Determination of the crystallization point of pure benzene
DIN EN ISO 4307:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA (ISO/DIS 4307:2021); German and English version prEN ISO 4307:2021
DIN 58984-1:1984 Special laboratory medicine; determination of inorganic substances in serum, plasma, urine and other body fluids; determination of calcium by atomic absorption spectrometry
DIN EN ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021); German version EN ISO 6717:2021
DIN 24550-6:1999 Fluid power - Hydraulic filters - Part 6: Test filter housings; dimensions
DIN EN ISO 15197:2015-12 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013); German version EN ISO 15197:2015 / Note: DIN EN ISO 15197 (2013-11) remains valid alongside this stand...
DIN-Fachbericht 74:1999
DIN EN ISO 2812-1:2007 Paints and varnishes - Determination of resistance to liquids - Part 1: Immersion in liquids other than water (ISO 2812-1:2007)English version of DIN EN ISO 2812-1:2007-05
DIN-Fachbericht CEN/TR 15138:2005 Petroleum products and other liquids - Guide to flash point testing; German version CEN/TR 15138:2005
DIN EN 15890:2010 Foodstuffs - Determination of patulin in fruit juice and fruit based purée for infants and young children - HPLC method with liquid/liquid partition cleanup and solid phase extraction and UV detection; German version EN 15890:2010
DIN EN 238:2004-04 Liquid petroleum products - Petrol - Determination of the benzene content by infrared spectrometry; German version EN 238:1996 + A1:2003
DIN 51350-2:2010 Testing of lubricants - Testing in the four-ball tester - Part 2: Determination of welding load of liquid lubricants
DIN 51350-2:2015 Testing of lubricants - Testing in the four-ball tester - Part 2: Determination of welding load of liquid lubricants
DIN EN 1371-2:2015 Founding - Liquid penetrant testing - Part 2: Investment castings

KR-KS, In Vitro Blood Tests

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 8637-3-2022 Extracorporeal systems for blood purification Part 3: Plasmafilters
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 15675-2020 Cardiovascular implants and artificial organs — Cardiopulmonary bypass systems — Arterial blood line filters
KS P ISO 20186-1-2022 Molecular in vitro diagnostic examinations — Specifications for pre-examination processes for venous whole blood — Part 1: Isolated cellular RNA
KS P ISO 16256-2017 Clinical laboratory testing and in vitro diagnostic test systems ─ Reference method for testing the in vitro activity of antimicrobial agents against yeast fungi involved in infectious diseases
KS M ISO 2812-1-2022 Paints and varnishes — Determination of resistance to liquids — Part 1: Immersion in liquids other than water
KS P ISO 15197-2017 In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
KS I ISO 11264-2016 Soil quality－Determination of herbicides－Method using HPLC with UV-detection
KS P ISO 15197-2017(2022) In vitro diagnostic test systems — Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
KS B 0816-2021(英文版) Method for liquid penetrant testing and classification of the penetrant indication

Indonesia Standards, In Vitro Blood Tests

SNI ISO 8638:2012 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
SNI ISO 15197:2009 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus

CEN - European Committee for Standardization, In Vitro Blood Tests

EN ISO 8637-2:2018 Extracorporeal systems for blood purification - Part 2: Extracorporeal blood circuit for haemodialysers@ haemodiafilters and haemofilters
EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA
EN ISO 20186-2:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA
PD CEN/TS 17305:2019 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA

American Society for Testing and Materials (ASTM), In Vitro Blood Tests

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 F1830-97(2005) Standard Practice for Selection of Blood for in vitro Evaluation of Blood Pumps
ASTM F2888-19 Standard Practice for Platelet Leukocyte Count—An In-Vitro Measure for Hemocompatibility Assessment of Cardiovascular Materials
ASTM F1830-19 Standard Practice for Collection and Preparation of Blood for Dynamic in vitro Evaluation of Hemolysis in Blood Pumps
ASTM E2680-09e1 Standard Test Method for Appearance of Clear, Transparent Liquids (Visual Inspection Procedure)
ASTM F2477-07 Standard Test Methods forin vitro Pulsatile Durability Testing of Vascular Stents
ASTM F2477-19 Standard Test Methods for in vitro Pulsatile Durability Testing of Vascular Stents
ASTM E433-71(2023) Standard Reference Photographs for Liquid Penetrant Inspection
ASTM E2680-09 Standard Test Method for Appearance of Clear, Transparent Liquids (Visual Inspection Procedure)
ASTM E2680-16 Standard Test Method for Appearance of Clear, Transparent Liquids (Visual Inspection Procedure)
ASTM E2680-09(2015) Standard Test Method for Appearance of Clear, Transparent Liquids (Visual Inspection Procedure)
ASTM D7620-10(2020) Standard Test Method for Determination of Total Sulfur in Liquid Hydrocarbon Based Fuels by Continuous Injection, Air Oxidation and Ultraviolet Fluorescence Detection
ASTM UOP678-04 Dissolved Molecular Oxygen in Liquid Hydrocarbons by Electrochemical Detection

British Standards Institution (BSI), In Vitro Blood Tests

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 8638:2014 Cardiovascular implants and extracorporeal systems. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
BS EN ISO 8637-2:2018 Tracked Changes. Extracorporeal systems for blood purification. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
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
12/30254337 DC BS ISO 8637 AMD1. 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
BS ISO 18242:2016 Cardiovascular implants and extracorporeal systems. Centrifugal blood pumps
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
16/30331650 DC BS EN ISO 8637-1. Extracorporeal systems for blood purification. Part 1. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
BS ISO 11658:2012 Cardiovascular implants and extracorporeal systems. Blood/tissue contact surface modifications for extracorporeal perfusion systems
BS ISO 8637-3:2018 Extracorporeal systems for blood purification. Plasmafilters
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 20186-3:2019 Molecular in-vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free DNA from plasma
BS EN ISO 20186-1:2019 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood - Isolated cellular RNA
PD CEN/TS 17742:2022 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood. Isolated circulating cell free RNA from plasma
PD CEN/TS 17747:2022 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood. DNA, RNA and proteins
BS EN ISO 20186-2:2019 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for venous whole blood - Isolated genomic DNA
23/30470634 DC BS ISO 8637-3. Extracorporeal systems for blood purification - Part 3. Plasmafilters
20/30424657 DC BS EN ISO 6717. In vitro diagnostic medical devices. Single-use containers for the collection of specimens, other than blood, from humans
BS EN ISO 15197:2015 Tracked Changes. In vitro diagnostic test systems. Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
BS EN ISO 2812-1:2007 Paints and varnishes - Determination of resistance to liquids - Immersion in liquids other than water
BS ISO 16604:2004 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
PD CEN/TS 17811:2022 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for urine and other body fluids. Isolated cell free DNA
BS EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
BS 7730:1994 Method for liquid penetrant inspection of metallic surgical implants
BS ISO 17593:2007 Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
PD CEN/TS 17390-2:2020 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood. Isolated DNA
BS EN ISO 6717:2021 Tracked Changes. In vitro diagnostic medical devices. Single-use containers for the collection of specimens from humans other than blood
BS ISO 4987:2020 Steel and iron castings. Liquid penetrant testing
PD CEN/TS 17390-1:2020 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood. Isolated RNA
BS ISO 24431:2007 Gas cylinders - Cylinders for compressed and liquefied gases (excluding acetylene) - Inspection at the time of filling
BS EN ISO 2812-1:2017 Tracked Changes. Paints and varnishes. Determination of resistance to liquids. Immersion in liquids other than water
PD CEN/TS 17390-3:2020 Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood. Preparations for analytical CTC staining
21/30421396 DC BS EN ISO 4307. Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for saliva. Isolated human DNA
BS EN ISO 4307:2021 Tracked Changes. Molecular in vitro diagnostic examinations. Specifications for pre-examination processes for saliva. Isolated human DNA
BS PD ISO/TS 17822-1:2014 $iI$in $iv$ii$it$ir$io diagnostic test systems. Qualitative nucleic acid-based $ii$in $iv$ii$it$ir$io examination procedures for detection and identification of microbial pathogens. General requirements, terms and definitions
BS EN ISO 15197:2003 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
BS EN ISO 15197:2013 In vitro diagnostic test systems. Requirements for blood-glucosemonitoring systems for self-testing in managing diabetes mellitus
BS PD CEN/TR 15138:2005 Petroleum products and other liquids - Guide to flash point testing
BS EN ISO 11755:2020 Gas cylinders. Cylinder bundles for compressed and liquefied gases (excluding acetylene). Inspection at time of filling

Canadian Standards Association (CSA), In Vitro Blood Tests

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)
CAN/CSA-ISO 8637:2012 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (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)
CSA ISO 15197-05-CAN/CSA:2005 Syst鑝es d'essais de diagnostic in vitro ?Exigences relatives aux syst鑝es d'autosurveillance de la glyc閙ie destin閟 ?la prise en charge du diab鑤e sucr镻remi鑢e 閐ition

AENOR, In Vitro Blood Tests

UNE-EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8638:2010)
UNE-EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637:2010, including Amendment 1 2013-04-01)
UNE-EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
UNE-EN ISO 15197:2013 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)
UNE-EN 13160-3:2004 Leak detection systems - Part 3: Liquid systems for tanks
UNE-EN 1371-2:2015 Founding - Liquid penetrant testing - Part 2: Investment castings

ES-AENOR, In Vitro Blood Tests

UNE 111-350-1989

European Committee for Standardization (CEN), In Vitro Blood Tests

EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers@ haemodiafilters and haemofilters
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 1283:1996 Haemodialysers, Haemodiafilters, Haemofilters, Haemoconcentrators and Their Extracorporeal Circuits
EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
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 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)
PD CEN/TS 16945:2016 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for metabolomics in urine@ venous blood serum and plasma
EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
FprCEN/TS 17742-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
prEN ISO 18703 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
CEN/TS 17742:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Isolated circulating cell free RNA from plasma
EN ISO 15197:2003 In vitro diagnostic test systems Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus ISO 15197:2003
EN ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)
FprCEN/TS 17747-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins
prCEN ISO/TS 18702 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins
CEN/TS 17747:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for exosomes and other extracellular vesicles in venous whole blood - DNA, RNA and proteins
CEN/TS 17811:2022 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNA
prEN ISO 18704 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for urine and other body fluids - Isolated cell free DNA
EN ISO 4307:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA (ISO 4307:2021)
EN ISO 11755:2020 Gas cylinders - Cylinder bundles for compressed and liquefied gases (excluding acetylene) - Inspection at time of filling (ISO 11755:2005)
CEN/TS 17390-2:2020 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 2: Isolated DNA
EN ISO 15197:2015 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2013)
CEN/TS 17390-1:2020 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNA
EN ISO 15197:2013 In vitro diagnostic test systems - Requirements for bloodglucose monitoring systems for self-testing in managing diabetes mellitus
EN ISO 10249:1999 Fluid Fertilizers - Preliminary Visual Examination and Preparation of Samples for Physical Testing
EN ISO 2812-1:1994 Paints and varnishes Determination of resistance to liquids Part 1: General methods ISO 2812-1: 1993
EN ISO 2812-1:2017 Paints and varnishes - Determination of resistance to liquids - Part 1: Immersion in liquids other than water (ISO 2812-1:2017)
EN ISO 2812-1:2007 Paints and varnishes - Determination of resistance to liquids - Part 1: Immersion in liquids other than water (ISO 2812-1:2007)
PD CEN/TS 16835-2:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 2: Isolated genomic DNA
PD CEN/TR 15138:2005 Petroleum products and other liquids Guide to flash point testing
PD CEN/TS 16835-1:2015 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for venous whole blood - Part 1: Isolated cellular RNA
PD CEN/TS 16835-3:2015 Molecular in vitro diagnostic e xaminations - Specifications for pre-examination processes for venous whole blood - Part 3: Isolated circulating cell free DNA from plasma

IN-BIS, In Vitro Blood Tests

IS 13878-1993 Extracorporeal blood circuit for haemodialysers, haemofilters and haemoconcentrators - specification
IS 12889-1989

Taiwan Provincial Standard of the People's Republic of China, In Vitro Blood Tests

CNS 14194-1998 Extracorporeal blood circuit for haemodialysers hasmofilters and haemoconcentrators
CNS 15035-2006 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus

RU-GOST R, In Vitro Blood Tests

GOST R ISO 8638-1999 Extracorporeal blood circuit for 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 ISO 17593-2011 Clinical laboratory testing and in vitro medical devices. Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
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 8.470-1982 State system for ensuring the uniformity of measurements. State verification schedule for means of measuring volume of liquid
GOST R ISO 15197-2015 In vitro diagnostic test systems. Requirements for blood glucose monitoring systems for self-testing in managing diabetes mellitus
GOST R 55991.6-2014 In vitro diagnostics medical devices. Part 6. Automatic analyzers for hematology tests. Technical requirements for public procurement
GOST R ISO 10893-4-2014 Seamless and welded steel tubes. Part 4. Liquid penetrant inspection for the detection of surface imperfections
GOST 13005-1967 Interferometers for determination of liqnid and gas concentration. Methods and means for verification

Professional Standard - Medicine, In Vitro Blood Tests

YY 0267-1995 Extracorporeal blood circuit for blood purification devices
YY 0267-2016 Extracorporeal circulation blood circuit of blood purification device for hemodialysis and related treatment
YY 0267-2008 Cardiovascular implants and artificial organs.Extracorporeal blood circuit for blood purification devices
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/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 0343-2002 Liquid penetrant inspection of metallic surgical implants
YY/T 0808-2010 Standard test methods for in vitro pulsatile durability testing of vascular stents
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

Danish Standards Foundation, In Vitro Blood Tests

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/ISO 23118:2021 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes in metabolomics in urine, venous blood serum and plasma
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 6717:2021 In vitro diagnostic medical devices – Single-use containers for the collection of specimens from humans other than blood
DS/ISO/TS 23810:2012 Cardiovascular implants and artificial organs - Checklist for preoperative extracorporeal circulation equipment setup
DS/ISO 4307:2021 Molecular in vitro diagnostic examinations – Specifications for pre-examination processes for saliva – Isolated human DNA
DS/ISO 16604:2005 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-X-174 bacteriophage
DS/EN ISO 15197:2013 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus
DS/EN ISO 2812-1:2007 Paints and varnishes - Determination of resistance to liquids - Part 1: Immersion in liquids other than water
DS/EN 13160-3:2003 Leak detection systems - Part 3: Liquid systems for tanks

Lithuanian Standards Office , In Vitro Blood Tests

LST EN 1283-2001 Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
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 15197:2004 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003)
LST EN ISO 15197:2004/AC:2005 In vitro diagnostic test systems - Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus (ISO 15197:2003)
LST EN 13160-3-2004 Leak detection systems - Part 3: Liquid systems for tanks

AT-ON, In Vitro Blood Tests

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)
OENORM EN ISO 4307:2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for saliva - Isolated human DNA (ISO/DIS 4307:2021)

IT-UNI, In Vitro Blood Tests

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 CEN/TS 17390-1-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 1: Isolated RNA
UNI CEN/TS 17390-2-2021 Molecular in vitro diagnostic examinations - Specifications for pre-examination processes for circulating tumor cells (CTCs) in venous whole blood - Part 2: Isolated DNA

Jilin Provincial Standard of the People's Republic of China, In Vitro Blood Tests

DB22/T 2915-2018 Technical requirements for blood testing of blood donor dogs

US-AAMI, In Vitro Blood Tests

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

Professional Standard - Public Safety Standards, In Vitro Blood Tests

GA 657-2006 Detection method for ABO blood type in human body fluid stains. Hemagglutination inhibition test
GA 656-2006 Detection method for ABO blood type in human blood(stains). Hemagglutination test, elution test
GA/T 1630-2019 Inductively Coupled Plasma Mass Spectrometry for Forensic Science Blood and Urine Tests for Five Elements including Chromium

CH-SNV, In Vitro Blood Tests

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)
SN EN ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)

American National Standards Institute （ANSI), In Vitro Blood Tests

ANSI/AAMI/ISO 8638:2010 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
ANSI/AAMI/ISO 11658:2012 Cardiovascular implants and extracorporeal systems - Blood/tissue contact surface modifications for extracorporeal perfusion systems

Group Standards of the People's Republic of China, In Vitro Blood Tests

T/CSBT 004-2019 Quality monitoring indicators of blood testing laboratory in blood transfusion service
T/SHSYCXH 7-2022 Test method of human monocyte populations from peripheral blood-Flow cytometry
T/SHDSGY 026-2023 Disposable blood extracorporeal circulation tubing
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/CVMA 14-2020 Hemagglutination inhibition detection method for duck Tembusu virus antibody
T/SHSYCXH 8-2022 Test method of human Natural Killer cells and Natural Killer T cells from peripheral blood-Flow cytometry
T/SHSYCXH 11-2022 Determination of free amino acids in serum—Liquid chromatography tandem mass spectrometry
T/CRHA 006-2022 Specification for mononuclear cell resource storage in healthy blood donors Part 3：Detection of donor blood samples
T/SZGIA 6.2-2019 Genomics Data Normalization Part 2: Noninvasive Prenatal Testing Data

RO-ASRO, In Vitro Blood Tests

STAS 11327/2-1983 RUBBER STOPPERS FOR BLOOD, PLASMA AND SOLUTION BOTTLES FOR INJECTIONS AND PERFUSIONS Apparence, smell and taste checking out
STAS 11326/7-1989 RUBBER STOPPERS FOR PARENTHERAL USE BLOOD AND PREPARATOION BOTTLES Microbiological proofing checking up
STAS 10041-1975 LIQUID PENETRANT FLOW DETECTION Terminology
STAS SR ISO 9583:1995 Implants for surgery. Non-destructive testing. Liquid penetrant inspection of metailic surgical implants
STAS 11326/8-1989 RUBBER STOPPERS FOR PARENTHERAL USE BLOOD AND PREPARATION BOTTLES Microbiological checking up of poisonous substances with antibacterian action
STAS SR ISO 9916:1995 Aluminium alloy and magnesium alloy castings. Liquid penetrant inspection

National Health Commission of the People's Republic of China, In Vitro Blood Tests

WS/T 806-2022 Basic technical standards for clinical blood and body fluid testing
WST 360:2011 Guidelines for detection of peripheral blood lymphocyte subsets by flow cytometry
GBZ/T 328-2023 Micronucleus detection method and exposure dose estimation standard of peripheral blood lymphocytes in occupational health examination of radiation workers

National Metrological Verification Regulations of the People's Republic of China, In Vitro Blood Tests

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

国家市场监督管理总局、中国国家标准化管理委员会, In Vitro Blood Tests

GB/T 19634-2021 In vitro diagnostic test systems—General technical requirements for blood-glucose monitoring systems for self-testing
GB/T 38165-2019 Detection of circulating cell-free DNA concentration in human peripheral blood—Real-time PCR method based on Alu sequence

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, In Vitro Blood Tests

GB/T 19634-2005 In vitro diagnostic test systems.General technical requirements for blood-glucose monitoring systems for self-testing
GB/T 19634-2005(XG1-2006) In vitro diagnostic test systems-General technical requirements for blood-glucose monitoring systems for self-testing AMD 1
GB/T 23209-2008 Determination of lutein in milk powder.HPLC-UV method
GB/T 18448.1-2001 Laboratory animal--Methods for examination of ectoparasites
GB/T 18089-2008 Isolation,identification and serum neutralization antibody test in Bluetongue virus
GB/T 30648.1-2014 Paints and varnishes.Determination of resistance to liquids.Part 1:Immersion in liquids other than water
GB/T 32945-2016 In Vitro Detection of Bovine Tuberculosis Diagnosis Interferon-γ Method
GB/T 20768-2006 Method for the determination of biogenic amines in fish and shrimp LC-UV detection method
GB/T 23196-2008 Determination of ferulic acid content in propolis.HPLC-UV method
GB/T 20754-2006 Method for the determination of phenylbutazone in livestock and poultry muscles LC-UV detection method
GB/T 42677-2023 Non-destructive testing of steel pipes Liquid penetrant testing of seamless and welded steel pipes for surface imperfections

National Metrological Technical Specifications of the People's Republic of China, In Vitro Blood Tests

JJF 1541-2015 Calibration Specification for Hemodialysis Equipment Tester

Anhui Provincial Standard of the People's Republic of China, In Vitro Blood Tests

DB34/T 4240-2022 Service Specifications for Third-Party Blood Testing Institutions
DB34/T 3642-2020 Technical regulations for rapid detection of Mycoplasma synovialum LAMP

Professional Standard - Commodity Inspection, In Vitro Blood Tests

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 1224-2003 Rapid Serum Agglutination Test for Antibody Detection of Mycoplasma Gallisepticum Infection
SN/T 2987-2011 Colloidal gold immunofiltration dot detection for cysticercosis cellulosae antibody
SN/T 1222-2003 Detection of antibodies against(pullorum disease)-Protocol of whole blood plate agglutination test
SN/T 1181.2-2003 Detection antibodies against foot and mouth disease virus-Protocol of micro-serum neutralization test
SN/T 1498-2004 Determination of magnesium L-ascorbyl-2-phosphate in cosmetics-Liquid chromatography
SN/T 3312-2012 Interferon-gamma release assay for the diagnosis of Mycobacterium tuberculosis in vitro

Military Standards (MIL-STD), In Vitro Blood Tests

DOD A-A-54964-1994 MONITORING SET, ARTERIAL BLOOD GAS SAMPLING AND PRESSURE

未注明发布机构, In Vitro Blood Tests

DIN EN 14252:2004 In-vitro diagnostics – disposable vessels for human specimens with the exception of blood samples; German version EN 14254:2004
DIN EN ISO 15197:2004 Test systems for in vitro diagnostics – requirements for blood glucose measuring systems for self-use in diabetes mellitus
BS EN ISO 11369:1997(2008)*BS 6068-2.61:1997 Water quality — Determination of selected plant treatment agents — Method using high performance liquid chromatography with UV detection after solid - liquid extraction

Occupational Health Standard of the People's Republic of China, In Vitro Blood Tests

GBZ/T 248-2014 Test and assessment of chromosomal aberrations on occupational health examinations for radiation workers
GBZ/T(卫生) 248-2014 Test and assessment of chromosomal aberrations on occupational health examinations for radiation workers

Professional Standard - Agriculture, In Vitro Blood Tests

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
农业部公告第1834号 New veterinary drugs: 1. Avian Leukosis Virus ELISA Antigen Detection Kit; 2. Ginseng Leaf Oral Liquid
农业部1855号公告-1-2012 Avian Leukosis Virus Subtype J ELISA Antibody Detection Kit (Imported Veterinary Drug Registration)

HU-MSZT, In Vitro Blood Tests

GOSTR, In Vitro Blood Tests

GOST R EN 14254-2010 In vitro diagnostic medical devices. Single-use receptacles for the collection of specimens, other than blood, from humans
GOST ISO 15197-2011 In vitro diagnostic test systems. Requirements for blood-glucose monitoring systems for self-testing in managing diabetes mellitus

FI-SFS, In Vitro Blood Tests

SFS 3287-1975 RIKKOMATON AINEENKOETUS.TUNKEUMANESTETARKASTUS. YLEISET OHJEET

Professional Standard - Hygiene , In Vitro Blood Tests

WS/T 360-2011 Guidelines for peripheral lymphocyte subsets by flow cytometry
WS/T 792-2021 Detection standard of antibody against Schistosoma japonicum—Enzyme-linked immunosorbent assay

Professional Standard - Machinery, In Vitro Blood Tests

JB/T 6902-2008 Methods for liquid penetrant examination of valves
JB/T 9358-1999 Test method for fixed wavelength (254nm) UV detector used in liquid chromatography

Sichuan Provincial Standard of the People's Republic of China, In Vitro Blood Tests

DB51/T 2304-2016 Detection method of Haemophilus parasuis indirect ELISA antibody

YU-JUS, In Vitro Blood Tests

JUS C.A7.083-1979 Non-destructive testing - Liquid penetrant testing of welded joints
JUS H.P4.003-1988 Testing of pesticides. Liquid parafin. Technical requirements and testing

Defense Logistics Agency, In Vitro Blood Tests

DLA A-A-59230 VALID NOTICE 2-2009 Fluid, Magnetic Particle Inspection, Suspension

Professional Standard - Petroleum, In Vitro Blood Tests

SY 6826-2011 Computational inspection of liquid pipelines

Inner Mongolia Provincial Standard of the People's Republic of China, In Vitro Blood Tests

DB15/T 2741-2022 Indirect ELISA method for detecting the antibody of Mansonella ovis hemolyticus

国家药监局, In Vitro Blood Tests

YY/T 1764-2021 Test methods for axial, bending and torsional durability of vascular stents in vitro
YY/T 1649.2-2019 Medical device and platelet interaction test Part 2: Determination of in vitro platelet activation products (β-TG, PF4 and TxB2)
YY/T 1728-2021 Reference method for in vitro activity testing of yeast-like fungal antimicrobials related to systemic infectious diseases for clinical laboratory testing and in vitro diagnostics

卫生健康委员会, In Vitro Blood Tests

WS/T 630-2018 Schistosoma japonicum antibody detection indirect red blood cell agglutination test

Xinjiang Provincial Standard of the People's Republic of China, In Vitro Blood Tests

DB65/T 4668-2023 Fluorescent chromatographic detection method for equine infectious anemia virus antibodies

ZA-SANS, In Vitro Blood Tests

SANS 5289:1987 Chlorides in solids and liquids, detection

Jiangsu Provincial Standard of the People's Republic of China, In Vitro Blood Tests

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
DB32/T 3762.6-2020 Novel Coronavirus Detection Technical Specifications Part 6: Colloidal Gold Immunochromatographic Detection Procedures for Serum IgM and IgG Antibodies
DB32/T 3762.5-2020 Novel Coronavirus Detection Technical Specifications Part 5: Serum IgM and IgG Antibody Enzyme-Linked Immunosorbent Detection Procedures

国家质量监督检验检疫总局, In Vitro Blood Tests

SN/T 4906-2017 Determination of alkylphenol disulfide in rubber by liquid chromatography-ultraviolet detection method
SN/T 4828-2017 Wessels-Brown disease antibody hemagglutination inhibition test detection method
SN/T 4577-2016 Cosmetic skin irritation testing method for in vitro testing of reconstructed human epidermal model

North Atlantic Treaty Organization Standards Agency, In Vitro Blood Tests

STANAG 4240-2003 LIQUID FUEL/EXTERNAL FIRE, MUNITION TEST PROCEDURES

Hubei Provincial Standard of the People's Republic of China, In Vitro Blood Tests

DB42/T 1110-2015 In vitro drug susceptibility testing procedures for Mycoplasma bovis
DB42/T 733-2011 IFN-γin vitro release assay

CN-CNCA, In Vitro Blood Tests

CNCA 08C-034-2001 Implementation Rules for Compulsory Certification of Medical Device Products Extracorporeal Circulation Pipeline of Blood Purification Devices

Professional Standard - Aerospace, In Vitro Blood Tests

QJ 3109-1999 Satellite liquid propellant safety testing regulations
QJ 3108-1999 Regulations on Safety Testing of Launch Vehicle Liquid Propellants

Military Standard of the People's Republic of China-General Armament Department, In Vitro Blood Tests

GJB 9359-2018 Liquid rocket engine test and detection methods

BR-ABNT, In Vitro Blood Tests

ABNT NBR NM 334-2012 Non-destructive testing - Liquid penetrant - Detection of discontinuities

SG-SPRING SG, In Vitro Blood Tests

CP 85-2000 CODE OF PRACTICE FOR Cylinders in bundles for permanent and liquefiable gases (excluding acetylene) -Inspection at time of filling

农业农村部, In Vitro Blood Tests

NY/T 3144-2017 Determination of 18 β-agonists in feed raw blood products by liquid chromatography-tandem mass spectrometry

Professional Standard - Nuclear Industry, In Vitro Blood Tests

EJ/T 296.2-2014 Determination of trace uranium in urine liquid fluorometry by ultraviolet
EJ/T 20057-2014 Determination of uranium concentration in atmospheric fallout.Liquid fluorometry by ultraviolet

国家食品药品监督管理局, In Vitro Blood Tests

YY/T 1564-2017 Test method for in vitro pulsating flow performance of cardiovascular implant pulmonary artery valved conduits

CZ-CSN, In Vitro Blood Tests

CSN ISO 9916:1994 Aluminium alloy and magnesium alloy castings. Liquid penetrant inspection

SE-SIS, In Vitro Blood Tests

SIS SS IEC 582:1981 Nuclear instrumentation - Dimensions of via/s for liquid scintillation counting

Professional Standard - Electron, In Vitro Blood Tests

SJ/T 11826-2022 Online detection method of electrostatic charge density in pipeline liquids