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Liquid UV Instruments

Liquid UV Instruments, Total:362 items.

In the international standard classification, Liquid UV Instruments involves: Medical equipment, Analytical chemistry, Radiation protection, Protection against fire, Organic chemicals, Measurement of volume, mass, density, viscosity, Metrology and measurement in general, Measurement of fluid flow, Environmental testing, Fuels, Laboratory medicine, Nuclear energy engineering, Sensory analysis, Vocabularies, Paints and varnishes, Pipeline components and pipelines, Semiconductor devices, Water quality, Thermodynamics and temperature measurements, Medical sciences and health care facilities in general, Integrated circuits. Microelectronics, Fluid power systems, Natural gas, Corrosion of metals, Fruits. Vegetables, Beverages, Prepackaged and prepared foods, Test conditions and procedures in general, Soil quality. Pedology, Aerospace electric equipment and systems, Products of the chemical industry, Kitchen equipment, Domestic safety, Pharmaceutics, Surface treatment and coating, Insulation, Plastics, Insulating fluids, Measurement of force, weight and pressure.


GM North America, Liquid UV Instruments

  • GM GMP.PVC.038-2003 PVC Liquid Castable, Flexible Skin, UV Stabilized
  • GMP.PVC.038-2011 PVC ?Liquid Castable, Flexible Skin, UV Stabilized Issue 3; Do Not Use on New Programs; Replaced by GMW16081

Professional Standard - Medicine, Liquid UV Instruments

  • YY 0327-2002 Human blood containers for UV rays transmission therapy for single use
  • YY 91060-1999 Vocabulary of biochemical instruments.UV-VIS spectrophotometry
  • YY 0267-2008 Cardiovascular implants and artificial organs.Extracorporeal blood circuit for blood purification devices

General Administration of Quality Supervision, Inspection and Quarantine of the People‘s Republic of China, Liquid UV Instruments

  • GB/T 13971-1992 Specification of ultra-violet gas analyzers
  • GB/T 13971-2013 Specification of ultraviolet gas analyzers
  • GB/T 25274-2010 Films for liquid crystal display(LCD).Determination of ultraviolet absorbance
  • GB/T 29791.3-2013 In vitro diagnostic medical devices.Information supplied by the manufacturer (labelling).Part 3:In vitro diagnostic instruments for professional use
  • GB/T 29791.5-2013 In vitro diagnostic medical devices.Information supplied by the manufacturer (labelling).Part 5:In vitro diagnostic instruments for selftesting
  • GB/T 17574.9-2006 Semiconductor devices.Integrated circuits.Part 2-9:Digital integrated circuits.Blank detail specification for MOS ultraviolet light erasable electrically programmable read-only memories

Professional Standard - Nuclear Industry, Liquid UV Instruments

  • 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

American Society for Testing and Materials (ASTM), Liquid UV Instruments

  • ASTM E2297-04(2010) Standard Guide for Use of UV-A and Visible Light Sources and Meters used in the Liquid Penetrant and Magnetic Particle Methods
  • ASTM G154-04 Standard Practice for Operating Fluorescent Light Apparatus for UV Exposure of Nonmetallic Materials
  • ASTM G154-06 Standard Practice for Operating Fluorescent Light Apparatus for UV Exposure of Nonmetallic Materials
  • ASTM G154-00ae1 Standard Practice for Operating Fluorescent Light Apparatus for UV Exposure of Nonmetallic Materials
  • ASTM G154-00a Standard Practice for Operating Fluorescent Light Apparatus for UV Exposure of Nonmetallic Materials
  • ASTM G154-00 Standard Practice for Operating Fluorescent Light Apparatus for UV Exposure of Nonmetallic Materials
  • ASTM G73-10 Standard Test Method for Liquid Impingement Erosion Using Rotating Apparatus
  • 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 D6625-13 Standard Practice for Conducting a Test of Protective Properties of Polish Applied to a Painted Panel Using Fluorescent UV-Condensation Light- and Water-Exposure Apparatus
  • ASTM D7133-05 Standard Test Method for Polyurethane Raw Materials: Instrumental Measurement of Tristimulus CIELAB Color and Yellowness Index of Liquids
  • ASTM D7133-16 Standard Test Method for Polyurethane Raw Materials: Instrumental Measurement of Tristimulus CIELAB Color and Yellowness Index of Liquids
  • ASTM D7133-21 Standard Test Method for Polyurethane Raw Materials: Instrumental Measurement of Tristimulus CIELAB Color and Yellowness Index of Liquids

BE-NBN, Liquid UV Instruments

Professional Standard - Petrochemical Industry, Liquid UV Instruments

  • SH/T 0409-1992 Determination of Aromatics Content in Liquid Paraffin (UV Spectrophotometry)

International Organization for Standardization (ISO), Liquid UV Instruments

  • 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 5494:1978 Sensory analysis — Apparatus — Tasting glass for liquid products
  • 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 18113-5:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing
  • ISO 18113-3:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use
  • ISO 18113-3:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
  • ISO 18113-5:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 5: In vitro diagnostic instruments for self-testing
  • 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/PRF 6923:1979 Determination of monomeric diisocyanate content in coating materials and similar products using HPLC-UV
  • ISO 8638:2004 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • ISO 6717:2021 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood
  • 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 6923:2023 Paints and varnishes — Determination of monomeric diisocyanate content in coating materials and similar products using high performance liquid chromatography with ultraviolet detection (HPLC-UV)
  • ISO 8637-3:2018 Extracorporeal systems for blood purification - Part 3: Plasmafilters
  • ISO 15212-2:2002 Oscillation-type density meters - Part 2: Process instruments for homogeneous liquids
  • ISO/TR 12148:2009 Natural gas - Calibration of chilled mirror type instruments for hydrocarbon dewpoint (liquid formation)
  • ISO 8536-10:2004 Infusion equipment for medical use - Part 10: Accessories for fluid lines for use with pressure infusion equipment
  • ISO 8536-9:2004 Infusion equipment for medical usePart 9:Fluid lines for use with pressure infusion equipment
  • ISO 8536-9:2015 Infusion equipment for medical use - Part 9: Fluid lines for single use with pressure infusion equipment
  • 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 8536-10:2015 Infusion equipment for medical use - Part 10: Accessories for fluid lines for single use with pressure infusion equipment
  • 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 4402:1977 Hydraulic fluid power; Calibration of liquid automatic particle-count instruments; Method using Air Cleaner Fine Test Dust contaminant
  • ISO 15212-2:2002/cor 1:2008 Oscillation-type density meters - Part 2: Process instruments for homogeneous liquids; Technical Corrigendum 1

CZ-CSN, Liquid UV Instruments

  • CSN 25 7501-1966 Volumetric measuring apparatuses for liquids. Common regulations
  • CSN 25 7503-1966 Flow volumetric measuring apparatuses for liquids. Basic regulations
  • CSN 18 0521-1967 Measuring instrumenta. Dimensions of cases for panel recording instrumenta
  • CSN 25 7502-1966 Dosing volumetric measuring apparatuses for liquids. Basic regulations
  • CSN 35 6567-1988 Instruments for measurement volume activity of radionuclides in liquids. General technical specifications
  • CSN ISO 2733:1995 Vitreous and porcelain enamels.Apparatus for testing with acid and neutral liquids and their vapours
  • CSN EN 60335-2-15-2005

HU-MSZT, Liquid UV Instruments

Professional Standard - Education, Liquid UV Instruments

  • JY/T 0420-2010 Experimental apparatus for the internal pressure of liquid

Korean Agency for Technology and Standards (KATS), Liquid UV Instruments

  • 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 B OIMLR 120-2006 Standard capacity measures for testing measuring systems for liquids other than water
  • KS P ISO 18113-3-2015(2020) In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 3: In vitro diagnostic instruments for professional use
  • KS P ISO 8637:2018 Cardiovascular implants and extracorporeal systems — Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • KS P ISO 8536-9:2010 Infusion equipment for medical use-Part 9:Fluid lines for use with pressure infusion equipment
  • KS P ISO 8536-9:2017 Infusion equipment for medical use－Part 9：Fluid lines for use with pressure infusion equipment
  • KS P ISO 18113-5-2015(2020) In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 5: In vitro diagnostic instruments for self-testing
  • KS I ISO TR 12148:2011 Natural gas－Calibration of chilled mirror type instruments for hydrocarbon dewpoint(liquid formation)
  • KS B ISO 15212-2:2006 Oscillation-type density meters－Part 2：Process instruments for homogeneous liquids
  • KS P ISO 8536-10:2010 Infusion equipment for medical use－Part 10：Accessories for fluid lines for use with pressure infusion equipment
  • KS P ISO 8536-10:2017 Infusion equipment for medical use－Part 10：Accessories for fluid lines for use with pressure infusion equipment
  • KS P ISO 15675:2020 Cardiovascular implants and artificial organs — Cardiopulmonary bypass systems — Arterial blood line filters
  • KS I ISO TR 12148-2011(2021) Natural gas－Calibration of chilled mirror type instruments for hydrocarbon dewpoint(liquid formation)
  • KS C IEC 60748-2-9:2002 Semiconductor devices－Integrated circuits－Part 2：Digital integrated circuits－Section 9：Blank detail specification for MOS ultraviolet light erasable electrically programmable read－only memories
  • KS C IEC 60748-2-9-2002(2017) Semiconductor devices－Integrated circuits－Part 2：Digital integrated circuits－Section 9：Blank detail specification for MOS ultraviolet light erasable electrically programmable read－only memories
  • KS C IEC 60748-2-9-2002(2022) Semiconductor devices－Integrated circuits－Part 2：Digital integrated circuits－Section 9：Blank detail specification for MOS ultraviolet light erasable electrically programmable read－only memories
  • KS C IEC 61311-2005(2015) Radiation protection instrumentation－Equipment for continuously monitoring beta and gamma emitting radionuclides in liquid effluents or in surface waters

Association Francaise de Normalisation, Liquid UV Instruments

  • 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 S90-304:1989 MEDICO-SURGICAL EQUIPMENT. HAEMODIALYSIS EQUIPMENT. OPERATING DATA.
  • NF EN 17178:2019 Produits pétroliers liquides - Détermination de la teneur en soufre volatil dans les gaz de pétrole liquéfiés par spectroscopie de fluorescence ultra-violette
  • NF S92-017:1995 IN VITRO DIAGNOSTIC SYSTEMS. REQUIREMENTS FOR USER MANUALS FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR HOME USE. (EUROPEAN STANDARD EN 592).
  • NF S92-016:1995 IN VITRO DIAGNOSTIC SYSTEMS. REQUIRMENTS FOR USER MANUELS FOR IN VITRO DIAGNOSTIC INSTRUMENTS FOR PROFESSIONAL USE. (EUROPEAN STANDARD EN 591).
  • 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 S92-010-5:2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5 : in vitro diagnostic instruments for self-testing.
  • NF S92-010-5*NF EN ISO 18113-5:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5 : in vitro diagnostic instruments for self-testing
  • NF EN ISO 7199:2017 Implants cardiovasculaires et organes artificiels - Échangeurs gaz/sang extracorporels (oxygénateurs)
  • 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 S92-010-3:2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3 : in vitro diagnostic instruments for professional use.
  • NF S92-010-3*NF EN ISO 18113-3:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3 : in vitro diagnostic instruments for professional use
  • NF S93-302*NF EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems - Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • NF EN ISO 18113-3:2012 Dispositifs médicaux de diagnostic in vitro - Informations fournies par le fabricant (étiquetage) - Partie 3 : instruments de diagnostic in vitro à usage professionnel
  • 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 15212-2:2002 Densimètres à oscillation - Partie 2 : instruments industriels pour liquides homogènes
  • NF EN ISO 18113-5:2012 Dispositifs médicaux de diagnostic in vitro - Informations fournies par le fabricant (étiquetage) - Partie 5 : instruments de diagnostic in vitro pour auto-tests
  • NF S92-036:2004 In vitro diagnostic medical devices - Single-use receptables for the collection of specimens, other than blood, from humans.
  • NF S93-123-9:2005 Infusion equipment for medical use - Part 9 : fluid lines for use with pressure infusion equipment.
  • NF EN ISO 7199/A1:2020 Implants cardiovasculaires et organes artificiels - Échangeurs gaz/sang extracorporels (oxygénateurs) - Amendement 1 : raccords
  • 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 B35-212-2*NF EN ISO 15212-2:2002 Oscillation-type density meters - Part 2 : process instruments for homogeneous liquids
  • NF S93-123-10:2005 Infusion equipment for medical use - Part 10 : accessories for fluid lines for use with pressure infusion equipment.
  • NF S93-123-9*NF EN ISO 8536-9:2015 Infusion equipment for medical use - Part 9 : fluid lines for single use with pressure infusion equipment
  • NF S93-123-10*NF EN ISO 8536-10:2015 Infusion equipment for medical use - Part 10 : accessories for fluid lines for single use with pressure infusion equipment
  • NF T75-634*NF EN 16344:2013 Cosmetics - Analysis of cosmetic products - Screening for UV filters in cosmetic products and quantitative determination of 10 UV-filters by HPLC
  • NF C27-120:1986 Fluids for electrotechnical applications. Halogenous isolating liquids for transformers, other than pcb. General. Test methods. Specifications.
  • NF S92-021*NF EN ISO 17511:2004 In vitro diagnostic medical devices - Measurement of quantities in biological samples - Metrological traceability of values assigned to calibrators and control materials

ES-UNE, Liquid UV Instruments

  • 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 17178:2020 Liquid petroleum products - Determination of the total volatile sulfur content in liquefied petroleum gases by ultraviolet fluorescence spectroscopy
  • 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 6717:2022 In vitro diagnostic medical devices - Single-use containers for the collection of specimens from humans other than blood (ISO 6717:2021)
  • UNE-EN ISO 15212-2:2002/AC:2010 Oscillation-type density meters - Part 2: Process instruments for homogeneous liquids (ISO 15212-2:2002/Cor 1:2008)
  • UNE-EN 50243:2023 Outdoor bushings for 24 kV and 36 kV and for 5 kA and 8 kA, for liquid filled transformers
  • UNE-EN 17550:2022 Animal feeding stuffs: Methods of sampling and analysis - Determination of carotenoids in animal compound feed and premixtures by high performance liquid chromatography - UV detection (HPLC-UV)

German Institute for Standardization, Liquid UV Instruments

  • 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 17178:2018 Liquid petroleum products - Determination of the total volatile sulfur content in liquefied petroleum gases by ultraviolet fluorescence spectroscopy; German and English version prEN 17178:2018
  • DIN EN 17178:2019-12 Liquid petroleum products - Determination of the total volatile sulfur content in liquefied petroleum gases by ultraviolet fluorescence spectroscopy; German version EN 17178:2019
  • 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 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 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 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 12804:1975 Laboratory glassware; densitiy hydrometers for liquefied gases of hydrocarbons
  • DIN 12770:1982 Laboratory glassware; liquid-in-glass thermometers; general requirements
  • DIN EN ISO 15212-2 Berichtigung 1:2009-07 Oscillation-type density meters - Part 2: Process instruments for homogeneous liquids (ISO 15212-2:2002); German version EN ISO 15212-2:2002, Corrigendum to DIN EN ISO 15212-2:2002-07; German version EN ISO 15212-2:2002/AC:2009
  • DIN EN ISO 15212-2:2002-07 Oscillation-type density meters - Part 2: Process instruments for homogeneous liquids (ISO 15212-2:2002); German version EN ISO 15212-2:2002
  • DIN 24550-6:1999-04 Fluid power - Hydraulic filters - Part 6: Test filter housings; dimensions
  • DIN EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
  • 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 6855-1:1992 Quality control of nuclear medicine instruments; radiation counting systems for measurements in vivo and in vitro
  • DIN 12790:1979 Laboratory glassware; hydrometers, principles of construction and adjustment
  • DIN 24550-2:2006-09 Fluid power - Hydraulic filters - Part 2: Filter elements and filter housings; Characteristics, requirements
  • DIN 24550-6:1999 Fluid power - Hydraulic filters - Part 6: Test filter housings; dimensions
  • 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 ISO 18113-3:2013 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2011
  • DIN EN ISO 18113-5:2013 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009); German version EN ISO 18113-5:2011
  • 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 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 EN 50243:2023-06 Outdoor bushings for 24 kV and 36 kV and for 5 kA and 8 kA, for liquid filled transformers; German version EN 50243:2022 / Note: Date of issue 2023-05-12*Intended as replacement for DIN EN 50243 (2003-01).
  • DIN EN 50243:2003-01 Outdoor bushings for 24 kV and 36 kV and for 5 kA and 8 kA, for liquid filled transformers; German version EN 50243:2002
  • DIN 51900-1:2000 Testing of solid and liquid fuels - Determination of gross calorific value by the bomb calorimeter and calculation of net calorific value - Part 1: Principles, apparatus, methods
  • DIN EN 50243:2003 Outdoor bushings for 24 kV and 36 kV and for 5 kA and 8 kA, for liquid filled transformers; German version EN 50243:2002
  • DIN EN ISO 15212-2:2002 Oscillation-type density meters - Part 2: Process instruments for homogeneous liquids (ISO 15212-2:2002); German version EN ISO 15212-2:2002
  • DIN IEC 62963:2020 Radiation protection instrumentation - X-ray computed tomography (CT) inspection systems of bottled/canned liquids (IEC 62963:2020)
  • DIN 45940-1130:1989 Harmonized system of quality assessment for electronic components; blank detail specification: MOS ultra-violet light erasable electrically programmable read only memories silicon monolithic circuits
  • DIN 51900-1:2000-04 Testing of solid and liquid fuels - Determination of gross calorific value by the bomb calorimeter and calculation of net calorific value - Part 1: Principles, apparatus, methods / Note: To be replaced by DIN 51900 (2022-06).
  • DIN EN 50181:2011-04 Plug-in type bushings above 1 kV up to 52 kV and from 250 A to 2,50 kA for equipment other than liquid filled transformers; German version EN 50181:2010 / Note: DIN EN 50181 (1998-07) remains valid alongside this standard until 2013-07-01.

GOSTR, Liquid UV Instruments

  • GOST ISO 20846-2016 Liquid petroleum products. Determination of sulfur content of automotive fuels. Ultraviolet fluorescence method
  • GOST R EN 592-2010 Instructions for use for in vitro diagnostic instruments for self-testing
  • GOST R EN 14254-2010 In vitro diagnostic medical devices. Single-use receptacles for the collection of specimens, other than blood, from humans
  • GOST 28725-1990 Instruments for measuring the level of liquids and loose materials. General technical requirements and test methods

RU-GOST R, Liquid UV Instruments

  • GOST R 8.658-2009 State system for ensuring the uniformity of measurements Instruments measuring the characteristics of ultraviolet radiation of solar bad Verification procedure
  • GOST ISO 8638-2012 Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemoconcentrators. Technical requirements and test methods
  • GOST R ISO 18113-5-2015 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 5. In vitro diagnostic instruments for self-testing
  • GOST R ISO 18113-3-2015 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 3. In vitro diagnostic instruments for professional use
  • GOST 24802-1981 Level meters for liquid and solids. Terms and definitions
  • GOST R ISO 8638-1999 Extracorporeal blood circuit for haemodialysers, haemofilters and haemoconcentrators. Technical requirements and test methods
  • GOST 25164-1996 Connections of instruments and devices with external hydraulic and gas lines. Types, basic parameters and dimensions. Technical requirements
  • GOST 25164-1982 Connections of SSI instruments and devices with external hydraulic and gas lines. Types, basic parameters and dimensions. Technical requirements
  • GOST R 55991.6-2014 In vitro diagnostics medical devices. Part 6. Automatic analyzers for hematology tests. Technical requirements for public procurement
  • GOST R 8.901-2015 State system for ensuring the uniformity of measurements. Instruments of measurement of characteristic of ultraviolet radiation for medical sources. Verification procedure
  • GOST 28165-1989 Laboratory instruments and apparatus made from glass. Water distilation apparatus. Evaporators. Rectification. Apparatus. General techical requirements
  • GOST R 55991.5-2014 In vitro diagnostics medical devices. Part 5. Automatic analyzers for blood gas, metabolite and acid-base balance assessment. Technical requirements for public procurement
  • GOST R 8.760-2011 State system for ensuring the uniformity of measurements. Measurement of energy and the effective characteristics ultraviolet radiation germicidal irradiators. Procedure of measurements
  • GOST R 8.641-2008 State sysem for ensuring the iniformity of measurements. State verification scheme for measuring instruments of the water solutions ion content by electrochemical methods (pX measuring instruments)
  • GOST 8.142-2013 State system for insuring the uniformity of measurements. The national traceability chain for instruments measuring the mass and volumetric (the mass and the volume) flow of liquid
  • GOST 29016-1991 Vitreous and porcelain enamels. Apparatus for testing with acid and neutral liquids and their vapours
  • GOST R 55991.1-2014 In vitro diagnostics medical devices. Part 1. Automatic analyzers for biochemical assays. Technical requirements for public procurement
  • GOST R 55991.2-2014 In vitro diagnostics medical devices. Part 2. Automatic analyzer for immunoassays. Technical requirements for public procurement
  • GOST R 55991.4-2014 In vitro diagnostics medical devices. Part 4. Automatic analyzers for coagulation tests. Technical requirements for public procurement
  • GOST R 8.899-2015 State system for ensuring the uniformity of measurements. Measurements of liquids and gases flow rate and quantity by means of orifice instruments. Verification of measurement procedure
  • GOST 8.606-2012 State system for ensuring the uniformity of measurements. State verification schedule for measuring instruments of aerosols, suspensions and powdery materials
  • GOST R 8.735.0-2011 State system for ensuring the uniformity of measurements. State verification schedule for instruments measuring the content of components in liquid and solid media. Basic principles
  • GOST 8.563.2-1997 State system for ensuring the uniformity of measurements. Measurement of liquids and gases flow rate and quantity by differential pressure method. Measurement procedure by orifice instruments
  • GOST R 55991.7-2014 In vitro diagnostics medical devices. Part 7. Automatic analyzers for general clinical tests. Technical requirements for public procurement
  • GOST R 55991.3-2014 In vitro diagnostics medical devices. Part 3. Automatic analyzers for biomolecular assays. Technical requirements for public procurement
  • GOST R 55992.1-2014 In vitro diagnostic medical devices for fluorescent and immunofluorescent analysis of ?dried spot? of newborn's blood. Part 1. Instruments and accessories for fluorescent and immunofluorescent analysis of ?dried spot? of newborn's blood. Technical require

KR-KS, Liquid UV Instruments

  • 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 P ISO 15675-2020 Cardiovascular implants and artificial organs — Cardiopulmonary bypass systems — Arterial blood line filters
  • KS I ISO TR 12148-2022 Natural gas Calibration of chilled mirror type instruments for hydrocarbon dewpoint(liquid formation)

Professional Standard - Machinery, Liquid UV Instruments

  • JB/T 9358-1999 Test method for fixed wavelength (254nm) UV detector used in liquid chromatography

Indonesia Standards, Liquid UV Instruments

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

CEN - European Committee for Standardization, Liquid UV Instruments

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

Professional Standard - Electron, Liquid UV Instruments

Taiwan Provincial Standard of the People's Republic of China, Liquid UV Instruments

  • CNS 14194-1998 Extracorporeal blood circuit for haemodialysers hasmofilters and haemoconcentrators

British Standards Institution (BSI), Liquid UV Instruments

  • 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 17178:2019 Liquid petroleum products. Determination of the total volatile sulfur content in liquefied petroleum gases by ultraviolet fluorescence spectroscopy
  • BS EN 1658:1997 Requirements for marking of in vitro diagnostic instruments
  • BS EN ISO 8637-2:2018 Tracked Changes. Extracorporeal systems for blood purification. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • BS 7516:1995 Nuclear instrumentation. Liquid-scintillation counting systems. Performance verification
  • BS EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems. Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters
  • BS EN 591:2001 Instructions for use for in vitro diagnostic instruments for professional use
  • BS EN ISO 18113-3:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for professional use
  • BS EN 1283:1996 Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
  • BS EN ISO 8637-1:2020 Extracorporeal systems for blood purification. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BS EN ISO 18113-5:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic instruments for self-testing
  • BS 1428-D4:1963 Microchemical apparatus. Volumetric analysis. Specification for capillary pipettes
  • BS ISO 8637-3:2018 Extracorporeal systems for blood purification. Plasmafilters
  • BS EN ISO 8637:2014 Cardiovascular implants and extracorporeal systems. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • BS EN 592:2002 Instructions for use for in vitro diagnostic instruments for self-testing
  • 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 IEC 60747-14-11:2021 Semiconductor devices - Semiconductor sensors. Test method of surface acoustic wave-based integrated sensors for measuring ultraviolet, illumination and temperature
  • 16/30331650 DC BS EN ISO 8637-1. Extracorporeal systems for blood purification. Part 1. Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators
  • 18/30352698 DC BS IEC 63085. Radiation protection instrumentation. System of spectral identification of liquids in transparent and semitransparent containers
  • 19/30390371 DC BS IEC 60747-14-11. Semiconductor devices. Part 14-11. Semiconductor sensors. Test method of surface acoustic wave based integrated sensor for measuring ultra violet, illumination and temperature
  • 18/30362458 DC BS IEC 60747-14-11. Semiconductor devices. Part 14-11. Semiconductor sensors. Test method of surface acoustic wave based integrated sensor for measuring ultra violet, illumination and temperature
  • 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 15212-2:2002 Oscillation-type density meters — Part 2: Process instruments for homogenous liquids
  • BS ISO 11916-1:2013 Soil quality. Determination of selected explosives and related compounds. Method using high-performance liquid chromatography (HPLC) with ultraviolet detection
  • 21/30416037 DC BS EN ISO 18113-3. In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) - Part 3. In vitro diagnostic instruments for professional use
  • BS IEC 62963:2020 Radiation protection instrumentation. X-ray computed tomography (CT) inspection systems of bottled/canned liquids
  • 21/30416045 DC BS EN ISO 18113-5. In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling) - Part 5. In vitro diagnostic instruments for self-testing
  • 23/30470634 DC BS ISO 8637-3. Extracorporeal systems for blood purification - Part 3. Plasmafilters
  • BS ISO 6923:2023 Paints and varnishes. Determination of monomeric diisocyanate content in coating materials and similar products using high performance liquid chromatography with ultraviolet detection (HPLC-UV)
  • BS EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
  • 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 10771-1:2002 Hydraulic fluid power - Fatigue pressure testing of metal pressure-containing envelopes - Test method
  • 21/30440597 DC BS EN 50243. Outdoor bushings for 24 kV and 36 kV and for 5 kA and 8 kA, for liquid filled transformers
  • BS EN 50243:2022 Tracked Changes. Outdoor bushings for 24 kV and 36 kV and for 5 kA and 8 kA, for liquid filled transformers
  • BS ISO TR 3313:1998 Measurement of fluid flow in closed conduits - Guidelines on the effects of flow pulsations on flow-measurement instruments
  • BS IEC 63085:2021 Radiation protection instrumentation. System of spectral identification of liquids in transparent and semitransparent containers (Raman systems)
  • 18/30335408 DC BS IEC 62963. Radiation protection instrumentation. Bottle / can liquid X-ray computed tomography (CT) inspection systems
  • BS CECC 90113:1987 Specification for harmonized system of quality assessment for electronic components - Blank detail specification - MOS ultra-violet light erasable electrically programmable read only memories silicon monolithic circuits
  • BS 3680-8H:1996 Measurement of liquid flow in open channels. Measuring instruments and equipment. Method of specifying the performance of hydrometric equipment
  • BS 3680-8D:1980 Measurement of liquid flow in open channels. Measuring instruments and equipment. Cableway system for stream gauging

SE-SIS, Liquid UV Instruments

  • SIS SMS 2957-1972 Vitreous enamels. Apparatus for testing with alkaline liquids
  • SIS SMS 2956-1972 Vitreous enamels. Apparatus for testing with acid and neutral liquids and vapours

ES-AENOR, Liquid UV Instruments

Canadian Standards Association (CSA), Liquid UV Instruments

  • 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)

AENOR, Liquid UV Instruments

  • UNE-EN ISO 8638:2014 Cardiovascular implants and extracorporeal systems - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters (ISO 8638:2010)
  • 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 18113-3:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
  • UNE-EN ISO 18113-5:2012 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
  • 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 ISO 15212-2:2003 Osscilation-type density meters. Part 2: Process instruments for homogenous liquids. (ISO 15212-2:2002)
  • UNE-EN 50181:2011 Plug-in type bushings above 1 kV up to 52 kV and from 250 A to 2,50 kA for equipment other than liquid filled transformers

未注明发布机构, Liquid UV Instruments

  • DIN EN 591:2001 Instructions for use for in vitro diagnostic instruments for professional use
  • DIN EN 14252:2004 In-vitro diagnostics – disposable vessels for human specimens with the exception of blood samples; German version EN 14254:2004
  • BS 5540-6:1990(2011) Evaluating particulate contamination of hydraulic fluids — Part 6 : Method of calibrating liquid automatic particle - count instruments (using mono - sized latex spheres)

IN-BIS, Liquid UV Instruments

European Committee for Standardization (CEN), Liquid UV Instruments

  • 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 18113-5:2011 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO 18113-5:2009)
  • EN 50018:1978 Electrical apparatus for potentially explosive atmospheres; Flameproof enclosure "d".
  • EN 50018:1978/A1:1979 Electrical apparatus for potentially explosive atmospheres; flameproof enclosure d
  • EN 50018:1978/A2:1982 Electrical apparatus for potentially explosive atmospheres; flameproof enclosure d
  • EN 50018:1978/A3:1985 Electrical apparatus for potentially explosive atmospheres; flameproof enclosure d
  • EN ISO 8637-1:2020 Extracorporeal systems for blood purification - Part 1: Haemodialysers, haemodiafilters, haemofilters and haemoconcentrators (ISO 8637-1:2017)
  • 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)
  • EN ISO 18113-3:2011 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009)
  • EN 14254:2004 In vitro diagnostic medical devices - Single-use receptacles for the collection of specimens, other than blood, from humans
  • EN ISO 18113-3:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use [Superseded: CEN EN 591]
  • EN ISO 18113-5:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing [Superseded: CEN EN 592]
  • prEN ISO 18113-3:2021 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/DIS 18113-3:2021)
  • FprEN ISO 18113-3 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/FDIS 18113-3:2022)
  • prEN ISO 18113-5:2021 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/DIS 18113-5:2021)
  • FprEN ISO 18113-5 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 5: In vitro diagnostic instruments for self-testing (ISO/FDIS 18113-5:2022)
  • EN ISO 15212-2:2002 Oscillation-type density meters - Part 2: Process instruments for homogenous liquids (ISO 15212-2:2002)
  • EN 2591-315:1998 Aerospace Series - Elements of Electrical and Optical Connection - Test Methods - Part 315: Fluid Resistance
  • EN ISO 15212-2:2002/AC:2009 Oscillation-type density meters - Part 2: Process instruments for homogeneous liquids (ISO 15212-2:2002/Cor 1:2008)

PL-PKN, Liquid UV Instruments

  • PN-EN 17178-2020-01 P Liquid petroleum products--Determination of the total volatile sulfur content in liquefied petroleum gases by ultraviolet fluorescence spectroscopy
  • PN G04026-1987 Liquids applied in hydraulik systems of mining machinery and equipment Tesi methods and fire resistant evaluation

Danish Standards Foundation, Liquid UV Instruments

  • DS/EN 591:1995 In vitro diagnostic systems - Requirements for ser manuals for in vitro diagnostic instruments or professional use
  • DS/EN 592:1995 In vitro diagnostic systems - Requirements for ser manuals for in vitro diagnostic instruments or home use
  • 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 15212-2/AC:2009 Oscillation-type density meters - Part 2: Process instruments for homogenous liquids
  • DS/EN ISO 15212-2:2002 Oscillation-type density meters - Part 2: Process instruments for homogenous liquids
  • DS/ISO 6717:2021 In vitro diagnostic medical devices – Single-use containers for the collection of specimens from humans other than blood
  • DS/EN 50181:2010 Plug-in type bushings above 1 kV up to 52 kV and from 250 A to 2,50 kA for equipment other than liquid filled transformers

GB-REG, Liquid UV Instruments

Lithuanian Standards Office , Liquid UV Instruments

  • LST EN 1283-2001 Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits
  • LST EN ISO 11985:2000 Ophthalmic optics - Contact lenses - Ageing by exposure to UV and visible radiation (in vitro method) (ISO 11985:1997)
  • LST EN ISO 15212-2:2003/AC:2009 Oscillation-type density meters - Part 2: Process instruments for homogeneous liquids (ISO 15212-2:2002/Cor 1:2008)
  • LST EN 50181-2010 Plug-in type bushings above 1 kV up to 52 kV and from 250 A to 2,50 kA for equipment other than liquid filled transformers

AT-ON, Liquid UV Instruments

  • ONORM EN 1283-1996 Haemodialysers,haemodiafilters,haemofilters,haemoconcentrators and their extracorporeal circuits
  • OENORM EN ISO 18113-3:2021 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO/DIS 18113-3:2021)

International Electrotechnical Commission (IEC), Liquid UV Instruments

  • IEC 61304:1994 Nuclear instrumentation - Liquid-scintillation counting systems - Performance verification
  • IEC 60747-14-11:2021 Semiconductor devices - Part 14-11: Semiconductor sensors - Test method of surface acoustic wave-based integrated sensors for measuring ultraviolet, illumination and temperature
  • IEC 63085:2021 Radiation protection instrumentation - System of spectral identification of liquids in transparent and semitransparent containers (Raman systems)
  • IEC 60748-2-9:1994 Semiconductor devices - Integrated circuits - Part 2: Digital integrated circuits; section 9: Blank detail specification for MOS ultraviolet light erasable electrically programmable read-only memories
  • IEC 62963:2020 Radiation protection instrumentation - X-ray computed tomography (CT) inspection systems of bottled/canned liquids

Society of Automotive Engineers (SAE), Liquid UV Instruments

  • SAE AIR898-1983 Liquid Automatic Particle Counters & Contamination Monitors

CENELEC - European Committee for Electrotechnical Standardization, Liquid UV Instruments

  • EN 50018:2000 Electrical Apparatus for Potentially Explosive Atmospheres - Flameproof Enclosures 'd'
  • EN 50018:1994 Electrical Apparatus for Potentially Explosive Atmospheres - Flameproof Enclosures 'd'

American Society of Mechanical Engineers (ASME), Liquid UV Instruments

  • ASME PTC 19.16-1965 Instruments and apparatus - Part 16: Density Determinations solids and liquids
  • ASME PTC 19.17-1965 Instruments and apparatus - Part 17: Determination of the viscosity of liquids

National Metrological Verification Regulations of the People's Republic of China, Liquid UV Instruments

US-AAMI, Liquid UV Instruments

  • 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

NZ-SNZ, Liquid UV Instruments

  • AS/NZS 1580.483.2:1994 Paints and Related Materials - Methods of Test Method 483.2: Resistance to Artificial Weathering - Fluorescent UV-Condensation Type Instruments

CH-SNV, Liquid UV Instruments

  • 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), Liquid UV Instruments

  • ANSI/AAMI/ISO 8638:2010 Cardiovascular implants and artificial organs - Extracorporeal blood circuit for haemodialysers, haemodiafilters and haemofilters

Defense Logistics Agency, Liquid UV Instruments

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

  • GB/T 6324.10-2020 Test method of organic chemical products—Part 10: Determination of trace sulfur in organic liquid products—Ultraviolet fluorescence method

Professional Standard - Environmental Protection, Liquid UV Instruments

  • HJ 1045-2019 Technical requirements and testing methods for portable ultraviolet absorption measuring instruments for flue gas from stationary pollution sources (sulfur dioxide and nitrogen oxides)

European Committee for Electrotechnical Standardization（CENELEC）, Liquid UV Instruments

  • EN 50243:2002 Outdoor Bushings for 24 kV and 36 kV and for 5 kA and 8 kA, for Liquid Filled Transformers

Hebei Provincial Standard of the People's Republic of China, Liquid UV Instruments

  • DB13/T 5127.14-2019 Determination of Toxic and Hazardous Substances in Extracts of Implantable Medical Devices - Visible-UV Spectrophotometry for Protein Migration

Standard Association of Australia （SAA）, Liquid UV Instruments

IT-UNI, Liquid UV Instruments

CN-CNCA, Liquid UV Instruments

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

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