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medical reagent

medical reagent, Total:500 items.

In the international standard classification, medical reagent involves: Occupational safety. Industrial hygiene, Explosion protection, Electrical equipment for working in special conditions, Birth control. Mechanical contraceptives, Medical equipment, Sterilization and disinfection, Non-ferrous metals, Radiation measurements, Pharmaceutics, Measurement of volume, mass, density, viscosity, Veterinary medicine, Products of the chemical industry, Rubber and plastics products, Vocabularies, Laboratory medicine, Fertilizers, Water quality, Microbiology, First aid, Medical sciences and health care facilities in general, Analytical chemistry, Pulps, Hospital equipment, Protective equipment, Shop fittings, Products of the textile industry, Organic chemicals, Plastics, Packaging materials and accessories.


Standard Association of Australia （SAA）, medical reagent

  • AS/NZS 2430.3.6:2004 Classification of hazardous areas - Examples of area classification - Laboratories, including fume cupboards and flammable medical agents
  • AS 2896:2011
  • AS 2896:1998 Medical gas systems - Installation and testing of non-flammable medical gas pipeline systems
  • AS 2896:2021 Medical gas systems — Installation and testing of non-flammable medical gas pipeline systems
  • AS/NZS 4537:1999 Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy
  • AS 4484:2016 Gas cylinders for industrial, scientific, medical and refrigerant use — Labelling and colour coding

Association Francaise de Normalisation, medical reagent

  • NF S97-034:1998 Additional lubricants and medicinal or non-medicinal preparations intended or likely to be placed in contact with male condoms. Compatibility. Specifications and test methods.
  • NF S97-034:2007 Additional lubricants and other medicinal or non-medicinal preparations intended or likely to be put in contact with natural rubber latex condoms - Compatibility - Specifications and test methods.
  • XP S92-042*XP ISO/TS 17518:2015 Medical Laboratories - Reagents for staining biological material - Guidance for users
  • NF C74-103*NF EN 60580:2004 Medical electrical equipment - Dose area product meters
  • XP ISO/TS 17518:2015 Laboratoire de biologie médicale - Réactifs pour la coloration de matériel biologique - Directives pour les utilisateurs
  • NF C74-103*NF EN IEC 60580:2020 Medical electrical equipment - Dose area product meters
  • NF EN 14675:2015 Antiseptiques et désinfectants chimiques - Essai quantitatif de suspension pour l'évaluation de l'activité virucide des antiseptiques et des désinfectants chimiques utilisés dans le domaine vétérinaire - Méthodes d'essai et prescriptions - (...
  • NF EN 14348:2005 Antiseptiques et désinfectants chimiques - Essai quantitatif de suspension pour l'évaluation de l'activité mycobactéricide des désinfectants chimiques utilisés en médecine, y compris les désinfectants pour instruments - Méthode d'essai et p...
  • NF EN 14204:2012 Antiseptiques et désinfectants chimiques - Essai quantitatif de suspension pour l'évaluation de l'activité mycobactéricide des antiseptiques et des désinfectants chimiques utilisés dans le domaine vétérinaire - Méthode d'essai et prescripti...
  • NF EN 1656:2019 Antiseptiques et désinfectants chimiques - Essai quantitatif de suspension pour l'évaluation de l'activité bactéricide des antiseptiques et des désinfectants chimiques utilisés dans le domaine vétérinaire - Méthode d'essai et exigences (pha...
  • NF T72-600:2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity in the medical area - Test method and requirements (phase 2, step 1)
  • NF EN 17422:2022 Antiseptiques et désinfectants chimiques - Essai quantitatif de surface pour l'évaluation des désinfectants de trayons utilisés dans le domaine vétérinaire - Méthode d'essai et prescriptions (phase 2, étape 2)
  • NF EN 14349:2012 Antiseptiques et désinfectants chimiques - Essai quantitatif de surface pour l'évaluation de l'activité bactéricide des antiseptiques et des désinfectants chimiques utilisés dans le domaine vétérinaire sur des surfaces non poreuses sans actio...
  • NF C74-205:1989 Medical electrical equipment. Dosimeters with ionization chambers as used in radiotherapy.
  • NF EN 17122:2019 Antiseptiques et désinfectants chimiques - Essai quantitatif de surfaces non poreuses pour l'évaluation de l'activité virucide des désinfectants et antiseptiques chimiques utilisés dans le domaine vétérinaire - Méthode d'essai et prescriptio...
  • NF EN 1657:2016 Antiseptiques et désinfectants chimiques - Essai quantitatif de suspension pour l'évaluation de l'activité fongicide ou levuricide des antiseptiques et des désinfectants chimiques utilisés dans le domaine vétérinaire - Méthode d'essai et pre...
  • NF T72-185:2007 Chemical disinfectants and antiseptics - Virucidal quantitative suspension test for chemical disinfectants and antiseptics used in human medicine - Test method and requirements (phase 2, step 1).
  • NF T72-185/IN1:2007 Chemical disinfectants and antiseptics - Virucidal quantitative suspension test for chemical disinfectants and antiseptics used in human medicine - Test method and requirements (phase 2, step 1).
  • NF T72-245*NF EN 14348:2005 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants - Test methods and requirements (phase 2, step 1)
  • NF EN 16777:2018 Antiseptiques et désinfectants chimiques - Essai quantitatif de surface non poreuse sans action mécanique pour l'évaluation de l'activité virucide des désinfectants chimiques utilisés dans le domaine médical - Méthode d'essai et exigences (p...
  • NF EN 17111:2018 Désinfectants chimiques et antiseptiques - Essai quantitatif de porte-germe pour l'évaluation de l'activité virucide pour instruments utilisés en médecine - Méthode d'essai et exigences (phase 2, étape 2)
  • FD S97-111*FD CEN/TR 15831:2009 Method for testing compression in medical hosiery
  • FD CEN/TR 15831:2009 Méthode d'essai de compression des bas médicaux
  • NF EN 17126:2018 Antiseptiques et désinfectants chimiques - Essai quantitatif de suspension pour l'évaluation de l'activité sporicide des désinfectants chimiques utilisés dans le domaine médical - Méthodes d'essai et exigences (phase 2, étape 1)
  • NF T72-175/IN1:2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)
  • NF T72-277:2014 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on porous surfaces without mechanical action - Test method and requirements (p
  • NF T72-204*NF EN 1657:2016 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticical activity of chemical desinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • NF T72-205*NF EN 17122:2019 Chemical disinfectants and antiseptics - Quantitative non-porous surface test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements - Phase2, step2
  • NF T72-277*NF EN 16437+A1:2019 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on porous surfaces without mechanical action - Test method and requirements (p
  • NF T72-277/IN1*NF EN 16437/IN1:2019 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on porous surfaces without mechanical action - Test method and requirements (p
  • NF EN ISO 23640:2015 Dispositifs médicaux de diagnostic in vitro - Évaluation de la stabilité des réactifs de diagnostic in vitro
  • NF T72-152*NF EN 1040:2006 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of basic bactericidal activity of chemical disinfectants and antiseptics - Test method and requirements (phase 1)
  • NF EN 16438:2014 Antiseptiques et désinfectants chimiques - Essai quantitatif de surface pour l'évaluation de l'activité fongicide ou levuricide des antiseptiques et des désinfectants chimiques utilisés dans le domaine vétérinaire sur des surfaces non poreuses...
  • NF T72-175*NF EN 13727+A2:2015 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)
  • NF T72-175/IN2*NF EN 13727/IN2:2015 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)
  • NF EN 14563:2009 Désinfectants et antiseptiques chimiques - Essai quantitatif de porte germe pour l'évaluation de l'activité mycobactéricide ou tuberculocide des désinfectants chimiques utilisés pour instruments en médecine humaine - Méthode d'essai et presc...
  • NF S92-032*NF EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
  • NF S92-032:2014 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
  • NF T72-196*NF EN 16777:2018 Chemical disinfectants and antiseptics - Quantitative non-porous surface test without mechanical action for the evaluation of virucidal activity of chemical disinfectants used in the medical area - Test method and requirements (phase 2/step 2)
  • NF T72-802:2005 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants and antiseptics used in veterinary field - Test method and requirements (phase 2, step 1).
  • NF T72-184:2006 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in veterinary field - Test method and requirements (phase 2, step 1).
  • NF T72-802*NF EN 14204:2012 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of mycobactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • NF T72-194:2008 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on non-porous surfaces without mechanical action - Test method and requirement
  • NF T72-246*NF EN 14563:2009 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2).
  • NF T72-175:2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)
  • NF S90-463:1982 Medical and surgical equipment. Surgical instruments. Scissors. Dimensions and tests.
  • NF S97-166:2014 Medical face masks - Requirements and test methods
  • NF S97-166*NF EN 14683+AC:2019 Medical face masks - Requirements and test methods
  • NF EN 14683+AC:2019 Masques à usage médical - Exigences et méthodes d'essai
  • NF T72-204:2006 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticical activity of chemical desinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1).
  • NF T72-206*NF EN 14562:2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in medical area - Test method and requirements (phase 2, step 2)
  • NF T72-207*NF EN 17111:2018 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of virucidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • NF EN ISO 19001:2013 Dispositifs médicaux de diagnostic in vitro - Informations fournies par le fabricant avec les réactifs de coloration de diagnostic in vitro utilisés en biologie
  • NF S93-130-1*NF EN ISO 9187-1:2010 Injection equipment for medical use - Part 1 : ampoules for injectables
  • NF T72-602*NF EN 14561:2007 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of bactericidal activity for instruments used in medical area - Test method and requirements (phase 2, step 2)
  • NF EN 14561:2007 Désinfectants chimiques et antiseptiques - Essai quantitatif de porte germe pour l'évaluation de l'activité bactéricide pour instruments utilisés en médecine humaine - Méthode d'essai et prescriptions (phase 2, étape 2)
  • NF C74-205*NF EN 60731:2012 Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy
  • NF C74-205/A1:2006 Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy.
  • NF T72-278*NF EN 16438:2014 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - (phase 2,
  • NF S98-103-3:2006 Sterilization of health care products - Radiation - Part 3 : guidance on dosimetric aspects.
  • NF EN 60731/A1:2022 Appareils électromédicaux - Dosimètres à chambres d'ionisation utilisés en radiothérapie
  • NF EN 60731:2012 Appareils électromédicaux - Dosimètres à chambre d'ionisation utilisés en radiothérapie
  • NF T72-194*NF EN 14349:2012 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test method and require
  • NF S97-500*NF EN ISO 18812:2003 Health informatics - Clinical analyser interfaces to laboratory information systems - Use profiles
  • NF T73-408*NF ISO 2456:1987 Surface active agents. Water used as a solvent for tests. Specifications and test methods.
  • NF S92-010-2:2010 In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2 : in vitro diagnostic reagents for professional use.
  • NF EN 17387:2021 Antiseptiques et désinfectants chimiques - Essai quantitatif pour l'évaluation de l'activité bactéricide et levuricide et/ou fongicide des désinfectants chimiques utilisés en médecine sur des surfaces non poreuses sans action mécanique - Mét...
  • NF T73-102:1993 Surface active agents. Industrial detergents containing solvent for washing hands. Specifications. Tests.
  • NF T72-208*NF EN 17126:2018 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of sporicidal activity of chemical disinfectants in the medical area - Test method and requirements (phase 2, step 1)
  • NF T72-185:2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity in the medical area - Test method and requirements (phase 2/step 1)
  • NF T72-182*NF EN 17387:2021 Chemical disinfectants and antiseptics - Quantitative test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants in the medical area on non-porous surfaces without mechanical action - Test method and requi
  • NF EN ISO 18113-2:2012 Dispositifs médicaux de diagnostic in vitro - Informations fournies par le fabricant (étiquetage) - Partie 2 : réactifs de diagnostic in vitro à usage professionnel
  • NF S94-402-1:1992 Examination of the corrosive efect of a decontaminant, cleaning agent or disinfectant on reusable medico-surgical instruments. Part 1 : metallic instruments.

Professional Standard - Medicine, medical reagent

  • YY 0299-2016 Medical ultrasonic couplants
  • YY 0299-1998 Medical ultrasonic couplants
  • YY 0299-2008 Medical ultrasonic couplant
  • YY/T 0976-2016/IEC 60731:2011 Ionization chamber dosimeters for medical electrical equipment radiotherapy
  • YY/T 0841-2023 Medical electrical equipment Periodic testing and post-repair testing of medical electrical equipment
  • YY/T 0841-2011 Medical electrical equipment.Recurrent test and test after repair of medical electrical equipment
  • YY/T 1842.8-2022
  • YY/T 0639-2008 In vitro diagnostic medical devices.Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
  • YY/T 1146-2016 Measurement methods of illuminance for medical optical instruments
  • YY 91146-1999 Test method of illumination intensity for medical optical instrument
  • YY/T 0866-2011 Total inward leakage determination method of protective face mask for medical use
  • YY/T 0907-2023 Requirements and test methods for medical needle-free syringes
  • YY/T 0907-2013 Needle-free injectors for medical use.Requirements and test methods

国家药监局, medical reagent

  • YY/T 0299-2022 Medical ultrasound coupling agent
  • YY/T 1733-2020 Guidelines for Dose Distribution Testing of Radiation Sterilization Irradiation Devices for Medical Devices
  • YY/T 0639-2019 In vitro diagnostic medical devices.Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology

BE-NBN, medical reagent

  • NBN-EN 375-1992 In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for professional use
  • NBN T 04-180-1983 Acetone for industrial use- Control test with Agulhon's reagent

Indonesia Standards, medical reagent

  • SNI 16-6360-2000 Pulse oximeters for medical use
  • SNI ISO 19001:2009 In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology

Group Standards of the People's Republic of China, medical reagent

  • T/WSJD 002-2019 Hygienic requirements for medical cleaning agents
  • T/CIAA 015-2021 Copper-based antimicrobial agents for hospital
  • T/CRIAC 0020-2020 Chemical reagent— Acetone for high performance liquid chromatography
  • T/CRIAC 0026-2020 Chemical reagent— Toluenefor high performance liquid chromatography
  • T/C3D 002-2023 Standard for test and evaluation of medical displays
  • T/TTGA 001-2020 Medical and civil protective equipment – Accelerated aging tests
  • T/CRIAC 0022-2020 Chemical reagent— n-Heptane for high performance liquid chromatography
  • T/CRIAC 0021-2020 Chemical reagent— Hexane for high performance liquid chromatography
  • T/CRIAC 0019-2020 Chemical reagent— Isopropyl alcohol for high performance liquid chromatography
  • T/CRIAC 0024-2020 Chemical reagent— Dichloromethane for high performance liquid chromatography
  • T/CRIAC 0025-2020 Chemical reagent— Trichloromethane for high performance liquid chromatography
  • T/CRIAC 0018-2020 Chemical reagent— Ethanol for high performance liquid chromatography
  • T/CRIAC 0023-2020 Chemical Reagents Reagents for High Performance Liquid Chromatography 2,2,4-Trimethylpentane

RU-GOST R, medical reagent

  • GOST R 59722-2021 Medical laboratories. Reagents for staining biological material. Guidance for users
  • GOST 4.492-1989 System of products quality indices. Biological veterinary preparations. Indices nomenclature
  • GOST R 50325-1992 Medical products. Dosimetric techniques for radiation sterilization
  • GOST IEC 60580-2011 Medical electrical equipment. Dose area product meters
  • GOST 33070-2014 Medical gloves. Method for determination of residual powdering agent
  • GOST R ISO 23640-2015 In vitro medical devices. Evaluation of stability of in vitro diagnostic reagents
  • GOST R 57146-2016 Medicines for medical applications. Studying for carcinogenicity of pharmaceuticals and excipients
  • GOST 17405-2016 Medicine remedies for veterinary use. Glanders antigen for use in the complement fixation test. Specifications
  • GOST R ISO 19001-2013 In vitro diagnostic medical devices. Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
  • GOST R 56328-2014 Medical equipment. Mobile complexes for medical purpose. General specifications and test methods
  • GOST R ISO 18472-2009 Sterilization of health care products. Biological and chemical indicators. Test equipment
  • GOST R 51088-2013 In vitro diagnostic medical devices. Reagents, kits, the test-systems, control materials, culture media. Requirements to devices and to supporting documentation
  • GOST R IEC 62353-2013 Medical electrical equipment. Recurrent test and test after repair of medical electrical equipment
  • GOST 4517-2016 Reagents. Methods for preparation of accessory reagents and solutions used for analysis
  • GOST 4517-1987 Reagents. Methods for preparation of accessory reagents and solutions used for analysis
  • GOST 31626-2012 Plaster of Paris for medical use. General technical requirements. Test methods
  • GOST ISO 5275-2017 Petroleum products and hydrocarbon solvents. Detection of thiols and other sulfur species. Doctor test
  • GOST R 53342-2009 Medical chisels. Technical requirements and test methods
  • GOST 31519-2012 Medical chisels. Technical requirements and test methods
  • GOST R ISO 18113-4-2015 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 4. In vitro diagnostic reagents for self-testing
  • GOST R ISO 18113-2-2015 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). Part 2. In vitro diagnostic reagents for professional use
  • GOST R ISO 11140-2-2001 Sterilization of health care products. Chemical indicators. Part 2. Test equipment and methods
  • GOST R ISO 11140-5-2008 Sterilization of health care products. Chemical indicators. Part 5. Class 2 indicators for air removal test sheets and packs
  • GOST 26368-1990 Medical luminaries. General technical requirements and test methods
  • GOST 28519-1990 Medical bone saws. General technical requirements and test methods
  • GOST ISO 8185-2012 Humidifiers for medical use. Technical requirements and test methods
  • GOST R ISO 8185-1999 Humidifiers for medical use. Technical requirements and test methods

Korean Agency for Technology and Standards (KATS), medical reagent

  • KS P ISO TS 17518:2018 Medical laboratories ─ Reagents for staining biological material ─ Guidance for users
  • KS C IEC 60580:2007 Medical electrical equipment－Dose area product meters
  • KS P ISO 9187-1:2009 Injection equipment for medical use-Part 1:Ampoules for injectables
  • KS P ISO 9187-1:2014 Injection equipment for medical use — Part 1: Ampoules for injectables
  • KS P ISO 23640:2019 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
  • KS C IEC 60731:2017 Medical electrical equipment－Dosimeters with ionization chambers as used in radiotherapy
  • KS C IEC 60731:2021 Medical electrical equipment — Dosimeters with ionization chambers as used in radiotherapy
  • KS P ISO 23640:2013 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
  • KS P 1002-2006 Cut and durability test methods for dressing scissors
  • KS P 1002-1980 Cut and durability test methods for dressing scissors
  • KS M 8532-2004 Potassium iodide for oxidant analysis
  • KS C IEC 60731:2012 Medical electrical equipment-Dosimeters with ionization chambers as used in radiotherapy
  • KS P ISO 17593-2009(2019) Clinical laboratory testing and in vitro medical devices－Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
  • KS P ISO 19001:2010 In virto diagnostic medical devices－Information supplied by the manufacturer with in vitro gnostic reagents for staining in biology
  • KS P ISO 19001:2017 In virto diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
  • KS M ISO 2456-2003(2018) Surface active agents－Water used as a solvent for tests－Specification and test methods
  • KS P SIO 18113-2-2012 In vitro diagnostic medical devices--Information supplied by the manufacturer (labelling)--Part 2：In vitro diagnostic reagents for professional use
  • KS M 8039-2008 Calcium chloride(for drying)
  • KS P ISO 18113-4-2015(2020) In vitro diagnostic medical devices — Information supplied by the manufacturer(labelling) — Part 4: In vitro diagnostic reagents for self-testing
  • KS P 1001-2006 Cut and durability test methods for surgical knives
  • KS P ISO 21649:2021 Needle-free injectors for medical use — Requirements and test methods

KR-KS, medical reagent

  • KS P ISO TS 17518-2018 Medical laboratories ─ Reagents for staining biological material ─ Guidance for users
  • KS C 9708-2022 Phantoms for magnetic resonance equipment for medical diagnosis
  • KS C IEC 60731-2017 Medical electrical equipment－Dosimeters with ionization chambers as used in radiotherapy
  • KS P ISO 23640-2019 In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
  • KS C IEC 60731-2021 Medical electrical equipment — Dosimeters with ionization chambers as used in radiotherapy
  • KS P ISO 19001-2017(2022) In virto diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
  • KS P ISO 19001-2017 In virto diagnostic medical devices — Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
  • KS M ISO 2456-2003(2023) Surface active agents－Water used as a solvent for tests－Specification and test methods
  • KS P ISO 21649-2021 Needle-free injectors for medical use — Requirements and test methods

International Organization for Standardization (ISO), medical reagent

  • ISO/TS 17518:2015 Medical laboratories — Reagents for staining biological material — Guidance for users
  • ISO 17593:2022 Clinical laboratory testing and in vitro medical devices — Requirements for in vitro monitoring systems for self-testing of oral anticoagulant therapy
  • ISO 19001:2002 In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
  • ISO 19001:2013 In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
  • ISO 18113-4:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 4: In vitro diagnostic reagents for self-testing
  • ISO 18113-2:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use

International Electrotechnical Commission (IEC), medical reagent

  • IEC 60580:2000 Medical electrical equipment – Dose area product meters (Edition 2.0)
  • IEC 60580:2003 Medical electrical equipment - Dose area product meters
  • IEC 60580:2019 RLV Medical electrical equipment - Dose area product meters
  • IEC 60731:2011+AMD1:2016 CSV Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy
  • IEC 62563-2:2021 Medical electrical equipment - Medical image display systems - Part 2: Acceptance and constancy tests for medical image displays
  • IEC 60731:1997 Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy
  • IEC 60731:2011 Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy
  • IEC 60731:2011/AMD1:2016 Amendment 1 - Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy

British Standards Institution (BSI), medical reagent

  • BS 1922:1987 Specification for glass dispensing measures for pharmaceutical purposes
  • PD ISO/TS 17518:2015 Medical laboratories. Reagents for staining biological material. Guidance for users
  • BS EN 14675:2006 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary field - Test method and requirements (phase 2, step 1)
  • BS EN 17422:2022 Chemical disinfectants and antiseptics. Quantitative surface test for the evaluation of teat disinfectants used in the veterinary area. Test method and requirements (phase 2 step 2)
  • BS EN 1656:2009 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • BS EN 1656:2010 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements (phase 2, step 1)
  • BS EN 16437:2014+A1:2019 Chemical disinfectants and antiseptics. Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on porous surfaces without mechanical action. Test method and…
  • BS EN 14476:2005 Chemical disinfectants and antiseptics - Virucidal quantitative suspension test for chemical disinfectants and antiseptics used in human medicine - Test method and requirements (phase 2, step 1)
  • BS EN 13624:2013 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity in the medical area. Test method and requirements (phase 2, step 1)
  • BS EN 13624:2003 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1)
  • 19/30358939 DC BS EN 17422. Chemical disinfectants and antiseptics. Quantitative surface test for the evaluation of teat disinfectants used in the veterinary area. Test method and requirements (phase 2 step 2)
  • BS EN 1656:2019 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements (phase 2, step 1)
  • BS EN 14561:2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of bactericidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • BS EN 14348:2005 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants - Test methods and requirements (phase 2, step 1)
  • BS EN 1657:2005 Chemical disinfectants and antiseptics — Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area — Test method and requirements (phase 2, step 1
  • BS EN 1657:2006 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • 23/30459164 DC BS EN 1657 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements (phase…
  • 23/30454767 DC BS EN 17122:2019/prA1 Chemical disinfectants and antiseptics. Quantitative nonporous surface test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements.…
  • BS EN 1657:2016 Tracked Changes. Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements (phase 2,...
  • BS EN 17122:2019 Chemical disinfectants and antiseptics. Quantitative non- porous surface test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements. Phase2, step2
  • BS EN 13727:2003 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (Phase 2/Step 1)
  • 23/30454764 DC BS EN 14349. Chemical disinfectants and antiseptics. Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action.…
  • BS EN 16777:2018 Chemical disinfectants and antiseptics. Quantitative non-porous surface test without mechanical action for the evaluation of virucidal activity of chemical disinfectants used in the medical area. Test method and requirements (phase 2/step 2)
  • 14/30303000 DC BS EN 16777. Chemical disinfectants and antiseptics. Quantitative non-porous surface test without mechanical action for the evaluation of virucidal activity of chemical disinfectants used in the medical area. Test method and requirements (phase…
  • BS EN 60731:1997 Medical electrical equipment. Dosimeters with ionization chambers as used in radiotherapy
  • BS EN 17126:2018 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of sporicidal activity of chemical disinfectants in the medical area. Test method and requirements (phase 2, step 1)
  • BS EN ISO 11138-2:2009 Sterilization of health care products - Biological indicators - Biological indicators for ethylene oxide sterilization processes
  • BS EN ISO 11138-2:2017 Sterilization of health care products. Biological indicators. Biological indicators for ethylene oxide sterilization processes
  • BS EN 14349:2004 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bacterial activity of chemical disinfectants and antiseptics used in the veterinary field on non-porous surfaces without mechanical action - Test method and requireme
  • BS EN 14349:2007 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on non-porous surfaces without mechanical action - Test method and requirement
  • BS EN 14675:2015 Tracked Changes. Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements (Phase 2, step 1)
  • 17/30357250 DC BS EN 17122. Chemical disinfectants and antiseptics. Quantitative non-porous surface test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements. Phase 2, step 2
  • BS EN 13727:2012+A1:2013 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of bactericidal activity in the medical area. Test method and requirements (phase 2, step 1)
  • BS EN 13727:2012+A2:2015 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of bactericidal activity in the medical area. Test method and requirements (phase 2, step 1)
  • BS EN 14476:2013 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of virucidal activity in the medical area. Test method and requirements (Phase 2/Step 1)
  • BS EN 14476:2013+A2:2019 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of virucidal activity in the medical area. Test method and requirements (Phase 2/Step 1)
  • BS 6734:2004 Antimicrobial efficacy of disinfectants for veterinary and agricultural use - Method
  • BS EN 14683:2014 Medical face masks. Requirements and test methods
  • BS EN 14683:2006 Surgical masks. Requirements and test methods
  • BS EN 14204:2004 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants and antiseptics used in the veterinary field - Test method and requirements (phase 2, step 1)
  • BS EN 14204:2012 Chemical disinfectants and antiseptics. Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants and antiseptics used in the veterinary area. Test method and requirements (phase 2, step 1)
  • BS EN 14562:2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • BS EN 17111:2018 Chemical disinfectants and antiseptics. Quantitative carrier test for the evaluation of virucidal activity for instruments used in the medical area. Test method and requirements (phase 2, step 2)
  • BS EN 14563:2008 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2)
  • BS EN 17387:2021 Chemical disinfectants and antiseptics. Quantitative test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants in the medical area on non-porous surfaces without mechanical action. Test method and require
  • BS EN ISO 18113-2:2011 In vitro diagnostic medical devices. Information supplied by the manufacturer (labelling). In vitro diagnostic reagents for professional use
  • BS EN ISO 19001:2013 In vitro diagnostic medical devices. Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
  • BS EN 60731:2012 Medical electrical equipment. Dosimeters with ionization chambers as used in radiotherapy
  • BS EN 16438:2014 Chemical disinfectants and antiseptics. Quantitative surface test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action. Test method
  • BS 6905:1987 Method for estimation of concentration of disinfectants used in 'dirty' conditions in hospitals by the modified Kelsey-Sykes test
  • BS EN 14349:2012 Chemical disinfectants and antiseptics. Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action. Test method and requireme
  • BS EN 16437:2014 Chemical disinfectants and antiseptics. Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on porous surfaces without mechanical action. Test method and requirements (pha
  • BS EN ISO 23640:2015 Tracked Changes. In vitro diagnostic medical devices. Evaluation of stability of in vitro diagnostic reagents
  • BS PD IEC/TR 62354:2014 General testing procedures for medical electrical equipment
  • 19/30392612 DC BS EN 17387. Chemical disinfectants and antiseptics. Quantitative non-porous surface test for the evaluation of bactericidal and/or yeasticidal and/or fungicidal activity of chemical disinfectants used in medical area. Part rev. Test method and require...
  • BS EN 455-1:2020+A1:2022 Medical gloves for single use - Requirements and testing for freedom from holes
  • BS 7236:1989 Code of practice for non-reclosable packaging for solid dose units of medicinal products

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

  • GB 27949-2011 General Requirements for Disinfectants for Medical Devices
  • GB/T 20012-2005 Medical electrical equipment.Dose area product meters
  • GB/T 17857-1999 Medical radiology--Terminology(Equipment for radiotherapy,nuclear medicine and radiation dosimetry)
  • GB/T 23680-2009 Method of testing desiccants for refrigerant drying
  • GB/T 14710-2009 Enviromental requirement and test methods for medical electrical equipment
  • GB/T 29791.4-2013 In vitro diagnostic medical devices.Information supplied by the manufacturer (labelling).Part 4:In vitro diagnostic reagents for selftesting
  • GB/T 29791.2-2013 In vitro diagnostic medical devices.Information supplied by the manufacturer (labelling).Part 2:In vitro diagnostic reagents for professional use
  • GB/T 603-2002 Chemical reagent--Preparations of reagent solutions for use in test methods
  • GB 15213-1994 Medical electron accelerators-Functional performance characteristics and test methods

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

  • GB 27949-2020 General requirements of disinfectant of medical instruments

European Committee for Standardization (CEN), medical reagent

  • EN 14204:2012 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • EN 13727:2003 Chemical disinfectants and antiseptics Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants for instruments used in the medical area Test method and requirements (phase 2, step 1)
  • EN 14675:2006 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • EN 13727:2012+A2:2015 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)
  • EN 13624:2003 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1)
  • EN 13624:2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity in the medical area - Test method and requirements (phase 2, step 1)
  • EN 14476:2013+A1:2015 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity in the medical area - Test method and requirements (Phase 2/Step 1)
  • EN 14476:2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity in the medical area - Test method and requirements (Phase 2/Step 1)
  • EN 1657:2005 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1) (Incorpor
  • EN 1657:2016 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2@ step 1)
  • EN 1657:2000 Chemical Disinfectants and Antiseptics - Quantitative Suspension Test for the Evaluation of Fungicidal Activity of Chemical Disinfectants and Antiseptics Used in Veterinary Field - Test Method and Requirements (Phase 2, Step 1)
  • CEN EN ISO 9187-1:2008 Injection equipment for medical use — Part 1: Ampoules for injectables
  • EN 14561:2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of bactericidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • EN ISO 23640:2013 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents
  • EN ISO 23640:2011 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents [Superseded: CEN EN 13640]
  • EN 14675:2015 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (Phase 2@ step 1)
  • CEN EN 13624-2003 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1)
  • EN 1656:2009 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • EN 16438:2014 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test metho
  • EN 14683:2014 Medical face masks - Requirements and test methods
  • HD 534 S1-1989 Medical electrical equipment; dosimeters with ionization chambers as used in radiotherapy
  • EN 14349:2012 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test method and require
  • EN 1656:2000 Chemical Disinfectants and Antiseptics - Quantitative Suspension Test for the Evaluation of Bactericidal Activity of Chemical Disinfectants and Antiseptics Used in Veterinary Field - Test Method and Requirements (Phase 2/Step 1)
  • EN 14348:2005 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants - Test methods and requirements (phase 2, step 1)
  • EN 14562:2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • EN 14563:2008 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2)
  • EN 13727:2012+A1:2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)
  • EN ISO 5359:2014 Anaesthetic and respiratory equipment - Lowpressure hose assemblies for use with medical gases (Incorporates Amendment A1: 2017)
  • EN ISO 19001:2013 In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
  • EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
  • EN 13727:2012 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1) (incorporates Amendment A1: 2013)
  • EN 17387:2021 Chemical disinfectants and antiseptics - Quantitative test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants in the medical area on non-porous surfaces without mechanical action - Test method and requi
  • EN 15040:2006 Chemicals used for treatment of water intended for human consumption - Antiscalants for membranes - Phosphonic acids and salts
  • EN 15041:2006 Chemicals used for treatment of water intended for human consumption - Antiscalants for membranes - Polyphosphates
  • EN ISO 5359:2014/A1:2017 Anaesthetic and respiratory equipment - Low-pressure hose assemblies for use with medical gases - Amendment 1 (ISO 5359:2014/Amd 1:2017)

CEN - European Committee for Standardization, medical reagent

  • EN 14204:2004 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2@ step 1)
  • EN 14476:2005 Chemical disinfectants and antiseptics - Virucidal quantitative suspension test for chemical disinfectants and antiseptics used in human medicine - Test method and requirements (phase 2@ step 1)
  • PREN 17122-2017 Chemical disinfectants and antiseptics - Quantitative nonporous surface test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements - Phase2@ step2
  • EN ISO 5359:2008 Low-pressure hose assemblies for use with medical gases (Incorporates Amendment A1: 2011)
  • EN 16777:2018 Chemical disinfectants and antiseptics - Quantitative non-porous surface test without mechanical action for the evaluation of virucidal activity of chemical disinfectants used in the medical area - Test method and requirements (phase 2/step 2)
  • EN 14683:2019 Medical face masks - Requirements and test methods
  • PREN 14683-2017 Medical face masks - Requirements and test methods
  • EN 14349:2007 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on nonporous surfaces without mechanical action - Test method and requirements
  • EN 14349:2004 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bacterial activity of chemical disinfectants and antiseptics used in veterinary field on nonporous surfaces without mechanical action - Test method and requirements (
  • EN 17111:2018 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of virucidal activity for instruments used in the medical area - Test method and requirements (phase 2@ step 2)
  • EN 14476:2013/PRA2:2016 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity in the medical area - Test method and requirements (Phase 2/Step 1)
  • EN 17126:2018 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of sporicidal activity of chemical disinfectants in the medical area - Test method and requirements (phase 2@ step 1)
  • EN 13795-2:2019 Surgical clothing and drapes - Requirements and test methods - Part 2: Clean air suits

ZA-SANS, medical reagent

  • SANS 1593:1994 Disinfectants based on glutaraldehyde for use on medical instruments
  • CKS 588-1983 SPECIFICATION for SODA LIME GRANULES WITH INDICATOR FOR HOSPITAL USE
  • SANS 5600:1978 Acute systemic toxicity of plastics for medical use

Danish Standards Foundation, medical reagent

  • DS/EN 60580:2001 Medical electrical equipment - Dose area product meters
  • DS/CEN/TR 15831:2009 Method for testing compression in medical hosiery
  • DS/EN 14349:2013 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test method and require
  • DS/EN 14204:2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • DS/EN 14561:2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of bactericidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • DS/EN 14675:2006 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • DS/EN 13727:2012 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)
  • DS/IEC/TR 62354:2009 General testing procedures for medical electrical equipment
  • DS/EN 62353:2008 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment
  • DS/EN 1657/AC:2007 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • DS/EN 1657:2006 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • DS/EN 28 325:1991 Dental rotary instruments - Test methods
  • DS/EN 14563:2009 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2)
  • DS/EN 60731:2012 Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy
  • DS/EN 14348:2005 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants - Test methods and requirements (phase 2, step 1)
  • DS/EN ISO 19001:2013 In vitro diagnostic medical devices - Information supplied by the manufacturer with in vitro diagnostic reagents for staining in biology
  • DS/EN 14562:2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • DS/EN ISO 21649:2009 Needle-free injectors for medical use - Requirements and test methods

European Committee for Electrotechnical Standardization（CENELEC）, medical reagent

  • EN IEC 60580:2020 Medical electrical equipment - Dose area product meters
  • EN 62353:2008 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment (Remains Current)
  • EN 62353:2014 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment
  • EN 60731:2012 Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy
  • EN 60580:2000 Medical Electrical Equipment Dose Area Product Meters

AENOR, medical reagent

  • UNE-EN 60580:2001 Medical electrical equipment - Dose area product meters.
  • UNE-CEN/TR 15831:2010 IN Method for testing compression in medical hosiery
  • UNE-EN 16437:2014 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on porous surfaces without mechanical action - Test method and requirements (p
  • UNE-EN 14204:2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • UNE-EN 14349:2013 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test method and require
  • UNE-EN 62353:2015 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment
  • UNE-EN 16438:2014 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test metho
  • UNE-EN 14683:2014 Medical face masks - Requirements and test methods
  • UNE-EN ISO 23640:2013 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
  • UNE-EN 14348:2005 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants - Test methods and requirements (phase 2, step 1)

German Institute for Standardization, medical reagent

  • DIN EN 60580:2001 Medical electrical equipment - Dose area product meters (IEC 60580:2000); German version EN 60580:2000
  • DIN EN 14675:2015-06 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (Phase 2, step 1); German version EN 146...
  • DIN EN 14675:2006 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1); English version of DIN E
  • DIN EN 17422:2022-09 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of teat disinfectants used in the veterinary area - Test method and requirements (phase 2 step 2); German version EN 17422:2022
  • DIN EN 17422:2022 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of teat disinfectants used in the veterinary area - Test method and requirements (phase 2 step 2)
  • DIN EN 17422:2019 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of teat disinfectants used in the veterinary area - Test method and requirements (phase 2 step 2); German and English version prEN 17422:2019
  • DIN EN ISO 9187-1:2008 Injection equipment for medical use - Part 1: Ampoules for injectables (ISO 9187-1:2006); German and English version EN ISO 9187-1:2008
  • DIN EN 1657:2016-11 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1); Germa...
  • DIN EN 16437:2019-12 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on porous surfaces without mechanical action - Test method and requirements...
  • DIN EN 14349:2023-02 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test method and requ...
  • DIN EN 14349:2013-02 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test method and requ...
  • DIN EN 14204:2013-02 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1); German version...
  • DIN EN 1656:2019-12 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1); German version EN ...
  • DIN EN 1656:2017 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1); German and English ve
  • DIN EN 16777:2019-03 Chemical disinfectants and antiseptics - Quantitative non-porous surface test without mechanical action for the evaluation of virucidal activity of chemical disinfectants used in the medical area - Test method and requirements (phase 2, step 2); German...
  • DIN EN 14561:2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of bactericidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2) English version of DIN EN 14561:2006-08
  • DIN EN 16437:2019 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on porous surfaces without mechanical action - Test method and requirements (p
  • DIN EN 14349:2023 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test method and require
  • DIN EN 1657:2006 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1); English
  • DIN EN 17122:2020-02 Chemical disinfectants and antiseptics - Quantitative non-porous surface test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements - Phase 2, step 2; German versio...
  • DIN EN ISO 23640:2015-12 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011); German version EN ISO 23640:2015 / Note: DIN EN ISO 23640 (2013-09) remains valid alongside this standard until 2018-06-30.
  • DIN 58959-10 Bb.1:1997 Quality management in medical microbiology - Part 10: Requirements for the use of control strains for testing reagents, dyes and biological materials; control strains for commonly used materials
  • DIN EN 16438:2014-07 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test me...
  • DIN EN 13727:2012 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1); German version EN 13727:2012
  • DIN EN 14675:2015 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (Phase 2, step 1); German version EN 14675:
  • DIN 58955-4:2006 Decontamination equipment for medical use - Part 4: Biological indicators; Requirements
  • DIN EN 13727:2015 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1); German version EN 13727:2012+A2:2015
  • DIN EN 13727:2014 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1); German version EN 13727:2012+A1:2013
  • DIN EN 16777:2019 Chemical disinfectants and antiseptics - Quantitative non-porous surface test without mechanical action for the evaluation of virucidal activity of chemical disinfectants used in the medical area - Test method and requirements (phase 2, step 2)
  • DIN EN 14563:2009-02 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2); Ge...
  • DIN EN 14348:2005 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants - Test methods and requirements (phase 2, step 1); Germa
  • DIN EN 17122/A1:2023-03 Chemical disinfectants and antiseptics - Quantitative non-porous surface test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements - Phase 2, step 2; German and En...
  • DIN EN 1657:2023-06 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1); Germa...
  • DIN EN 1657:2023 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1); Germa...
  • DIN EN 14683:2019-10 Medical face masks - Requirements and test methods; German version EN 14683:2019+AC:2019
  • DIN 8948:1998 Desiccants for refrigerant drying - Testing
  • DIN EN 14348:2005-04 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants - Test methods and requirements (phase 2, step 1); Ge...
  • DIN EN 14562:2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2) English version of DIN EN 14562:2006-08
  • DIN EN 17111:2018 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of virucidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • DIN EN 17111:2018-12 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of virucidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2); German version EN 17111:2018
  • DIN EN 14563:2009 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2);Englis
  • DIN EN 14561:2006-08 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of bactericidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2); German version EN 14561:2006
  • DIN 58940-2:1990 Medical microbiology; methods for the determination of susceptibility of pathogens (except mycobacteria) to antimicrobial agents; carrier of agents for agar diffusion test
  • DIN EN 1657:2016 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1); German v
  • DIN EN 16437:2014 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on porous surfaces without mechanical action - Test method and requirements (p
  • DIN EN 1657 Berichtigung 1:2007 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1); German v
  • DIN EN 16615:2015-06 Chemical disinfectants and antiseptics - Quantitative test method for the evaluation of bactericidal and yeasticidal activity on non-porous surfaces with mechanical action employing wipes in the medical area (4-field test) - Test method and requirement...
  • DIN EN 14204:2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1); German version EN
  • DIN EN 1656:2010 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area - Test method and requirements (phase 2, step 1); German version EN 1656:20
  • DIN EN 13624:2019 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity in the medical area - Test method and requirements (phase 2, step 1); German and English version prEN 13624:2019
  • DIN EN 13624:2022-08 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity in the medical area - Test method and requirements (phase 2, step 1); German version EN 13624:2021
  • DIN EN IEC 62563-2:2020-12 Medical electrical equipment - Medical image display systems - Part 2: Acceptance and constancy tests (IEC/CDV 62563-2:2020); German and English version prEN IEC 62563-2:2020 / Note: Date of issue 2020-11-20
  • DIN EN 16615:2015 Chemical disinfectants and antiseptics - Quantitative test method for the evaluation of bactericidal and yeasticidal activity on non-porous surfaces with mechanical action employing wipes in the medical area (4-field test) - Test method and requirements (
  • DIN EN 17387:2021-10 Chemical disinfectants and antiseptics - Quantitative test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants in the medical area on non-porous surfaces without mechanical action - Test method and re...
  • DIN EN 17387:2019 Chemical disinfectants and antiseptics - Quantitative non-porous surface test for the evaluation of bactericidal and/or yeasticidal and/or fungicidal activity of chemical disinfectants used in medical area - Part rev: Test method and requirements without
  • DIN 58959-6 Beiblatt 2:2022 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing; Supplement 2: Recommended test organisms for frequently used testing reagents, dyes and biological ma
  • DIN 58959-6 Beiblatt 2:2021 Medical microbiology - Quality management in medical microbiology - Part 6: Requirements relating to test organisms and their use in performance testing; Supplement 2: Recommended test organisms for frequently used testing reagents, dyes and biological ma
  • DIN EN 17846:2022 Chemical disinfectants and antiseptics - Quantitative test method for the evaluation of sporicidal activity against Clostridioides difficile on non-porous surfaces with mechanical action employing wipes in the medical area (4-field test) - Test method and
  • DIN EN 14562:2006-08 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2); German version EN 14562:2006
  • DIN EN 16438:2014 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test metho
  • DIN EN 17126:2019 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of sporicidal activity of chemical disinfectants in the medical area - Test method and requirements (phase 2, step 1)
  • DIN EN 17126:2019-02 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of sporicidal activity of chemical disinfectants in the medical area - Test method and requirements (phase 2, step 1); German version EN 17126:2018
  • DIN EN 12933:2008 Chemicals used for treatment of water intended for human consumption - Chemicals for emergency use - Trichloroisocyanuric acid; English version of DIN EN 12933:2008-10
  • DIN EN 17846:2022-06 Chemical disinfectants and antiseptics - Quantitative test method for the evaluation of sporicidal activity against Clostridioides difficile on non-porous surfaces with mechanical action employing wipes in the medical area (4-field test) - Test method ...
  • DIN EN 17387:2021 Chemical disinfectants and antiseptics - Quantitative test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants in the medical area on non-porous surfaces without mechanical action - Test method and requi
  • DIN 58959-10:1997 Quality management in medical microbiology - Part 10: Requirements for the use of control strains for testing reagents, dyes and biological materials
  • DIN 58940-4 Bb.1:2004 Medical microbiology - Susceptibility testing of pathogens to antimicrobial agents - Part 4: Evaluation classes of the minimum inhibitory concentration - MIC-breakpoints of antibacterial agents
  • DIN 58959-17 Bb.1:1997 Quality management in medical microbiology - Part 17: Requirements for the use of control strains for the examination of mycobacteria; control strains for commonly used culture media, reagents and test

ES-UNE, medical reagent

  • UNE-EN 17422:2023 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of teat disinfectants used in the veterinary area - Test method and requirements (phase 2 step 2)
  • UNE-EN 16437:2014+A1:2020 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on porous surfaces without mechanical action - Test method and requirements...
  • UNE-EN 14675:2015 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (Phase 2, step 1)
  • UNE-EN 1656:2020 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • UNE-EN 17122:2020 Chemical disinfectants and antiseptics - Quantitative non-porous surface test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements - Phase2, step2
  • UNE-EN ISO 23640:2015 In vitro diagnostic medical devices - Evaluation of stability of in vitro diagnostic reagents (ISO 23640:2011)
  • UNE-EN 16777:2019 Chemical disinfectants and antiseptics - Quantitative non-porous surface test without mechanical action for the evaluation of virucidal activity of chemical disinfectants used in the medical area - Test method and requirements (phase 2/step 2)
  • UNE-EN 1657:2016 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • UNE-EN 14683:2019+AC:2019 Medical face masks - Requirements and test methods
  • UNE-EN 17111:2019 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of virucidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • UNE-EN 14563:2009 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2)
  • UNE-EN 14561:2007 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of bactericidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • UNE-EN 60731:2012/A1:2022 Medical electrical equipment - Dosimeters with ionization chambers as used in radiotherapy (Endorsed by Asociación Española de Normalización in September of 2022.)
  • UNE-EN 16615:2015 Chemical disinfectants and antiseptics - Quantitative test method for the evaluation of bactericidal and yeasticidal activity on non-porous surfaces with mechanical action employing wipes in the medical area (4- field test) - Test method and requiremen...
  • UNE-EN 13624:2022 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity in the medical area - Test method and requirements (phase 2, step 1)
  • UNE-EN 17387:2022 Chemical disinfectants and antiseptics - Quantitative test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants in the medical area on non-porous surfaces without mechanical action - Test method and re...
  • UNE-EN 14562:2007 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • UNE-EN 17126:2019 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of sporicidal activity of chemical disinfectants in the medical area - Test method and requirements (phase 2, step 1)

PL-PKN, medical reagent

  • PN-EN 17111-2018-12 P Chemical disinfectants and antiseptics -- Quantitative carrier test for the evaluation of virucidal activity for instruments used in the medical area -- Test method and requirements (phase 2, step 2)
  • PN C04286-1971 General test methods of rubber products for medical use

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

BR-ABNT, medical reagent

国家食品药品监督管理局, medical reagent

  • YY/T 0976-2016 Ionization chamber dosimeter for medical electrical equipment for radiotherapy
  • YY/T 1612-2018 Test method for medical sterilization steam quality

Lithuanian Standards Office , medical reagent

  • LST EN 14349-2004 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bacterial activity of chemical disinfectants and antiseptics used in veterinary field on non-porous surfaces without mechanical action - Test method and requirements
  • LST EN 14349-2013 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test method and require
  • LST EN 14204-2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • LST EN 16437-2014 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of bactericidal activity of chemical disinfectants and antiseptics used in veterinary area on porous surfaces without mechanical action - Test method and requirements (p
  • LST EN 14561-2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of bactericidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • LST EN 62353-2015 Medical electrical equipment - Recurrent test and test after repair of medical electrical equipment (IEC 62353:2014)
  • LST EN 14675-2006 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • LST EN 13727-2012 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)
  • LST EN 13624-2004 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal activity of chemical disinfectants for instruments used in the medical area - Test method and requirements (phase 2, step 1)
  • LST EN 1657-2006 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • LST EN 1657-2006/AC-2007 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area - Test method and requirements (phase 2, step 1)
  • LST EN 16438-2014 Chemical disinfectants and antiseptics - Quantitative surface test for the evaluation of fungicidal or yeasticidal activity of chemical disinfectants and antiseptics used in the veterinary area on non-porous surfaces without mechanical action - Test metho
  • LST EN 14476-2013 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of virucidal activity in the medical area - Test method and requirements (Phase 2/Step 1)
  • LST EN 13727-2012+A1-2014 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of bactericidal activity in the medical area - Test method and requirements (phase 2, step 1)
  • LST EN 14563-2009 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of mycobactericidal or tuberculocidal activity of chemical disinfectants used for instruments in the medical area - Test method and requirements (phase 2, step 2)
  • LST EN 14348-2005 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of mycobactericidal activity of chemical disinfectants in the medical area including instrument disinfectants - Test methods and requirements (phase 2, step 1)
  • LST EN 16615-2015 Chemical disinfectants and antiseptics - Quantitative test method for the evaluation of bactericidal and yeasticidal activity on non-porous surfaces with mechanical action employing wipes in the medical area (4- field test) - Test method and requirements
  • LST EN 14562-2006 Chemical disinfectants and antiseptics - Quantitative carrier test for the evaluation of fungicidal or yeasticidal activity for instruments used in the medical area - Test method and requirements (phase 2, step 2)
  • LST EN 17387-2021 Chemical disinfectants and antiseptics - Quantitative test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants in the medical area on non-porous surfaces without mechanical action - Test method and requi

American Society for Testing and Materials (ASTM), medical reagent

  • ASTM E1327-90(1995)e1 Standard Test Method for Evaluation of Health Care Personnel Handwash Formulations by Utilizing Fingernail Regions
  • ASTM D817-96(2004)e1 Standard Test Methods of Testing Cellulose Acetate Propionate and Cellulose Acetate Butyrate
  • ASTM D8179-18 Standard Guide for Characterizing Detergents for the Cleaning of Clinically-used Medical Devices
  • ASTM E2755-22 Standard Test Method for Determining the Bacteria-Eliminating Effectiveness of Healthcare Personnel Hand Rub Formulations Using Hands of Adults
  • ASTM E2755-15 Standard Test Method for Determining the Bacteria-Eliminating Effectiveness of Healthcare Personnel Hand Rub Formulations Using Hands of Adults
  • ASTM D5151-11 Standard Test Method for Detection of Holes in Medical Gloves
  • ASTM F640-79(2000) Standard Test Methods for Radiopacity of Plastics for Medical Use
  • ASTM F640-23 Standard Test Methods for Determining Radiopacity for Medical Use
  • ASTM D5151-19 Standard Test Method for Detection of Holes in Medical Gloves
  • ASTM D5151-19(2023) Standard Test Method for Detection of Holes in Medical Gloves

Taiwan Provincial Standard of the People's Republic of China, medical reagent

  • CNS 14821-2004 Method of test for nonwoven fabrics of medical use
  • CNS 12595-1989 Method of Test for Cutting and Durability for Surgical Knives
  • CNS 14777-2003 Method of test for air exchange pressure of medical face mask

国家药品监督管理局, medical reagent

  • YY/T 1579-2018 In vitro diagnostic medical devices and in vitro diagnostic reagent stability evaluation

US-AAMI, medical reagent

Shanxi Provincial Standard of the People's Republic of China, medical reagent

  • DB14/T 2254-2020 Regulations on cold storage and freezing management of clinical in vitro diagnostic reagents in medical institutions

Hebei Provincial Standard of the People's Republic of China, medical reagent

  • DB13/T 1283.4-2010 Medical Imaging Diagnosis and Treatment Technical Standards Part 4: Guidelines for the Application of Contrast Agents in Medical Imaging

未注明发布机构, medical reagent

  • NF S90-463 Medical surgical equipment. Surgical medical instruments. Scissors. Dimensions and tests.
  • DIN EN 13624:2004 Chemical disinfectants and antiseptics – Quantitative suspension test to test the fungicidal effect of chemical disinfectants for instruments in the human medical sector – Test methods and requirements (Phase 2, Level 1); German version EN 13624:2003

Japanese Industrial Standards Committee (JISC), medical reagent

  • JIS T 0202:1979 Cut and durability test methods for dressing scissors
  • JIS K 8001:2009 General rule for test methods of reagents
  • JIS K 8001:2015 General rule for test methods of reagents
  • JIS K 8001:2017 General rules for test methods of reagents
  • JIS L 1912:1997 Test methods for nonwoven fabrics of medical use
  • JIS T 3226-1:2005 Pen-injectors for medical use -- Part 1: Pen-injectors for medical use -- Requirements and test methods
  • JIS T 3226-1:2011 Pen-injectors for medical use -- Part 1: Pen-injectors for medical use -- Requirements and test methods
  • JIS K 4822:2001 Reagents for stability tests of explosives
  • JIS K 4822:2019 Reagents for stability tests of explosives
  • JIS K 8124:2018 Calcium chloride (for drying) (Reagent)
  • JIS T 11140-1:2013 Sterilization of health care products.Chemical indicators.Part 1: General requirements
  • JIS T 3226-1:2015 Needle-based injection systems for medical use -- Part 1: Needle-based injection systems -- Requirements and test methods

国家卫生计生委, medical reagent

  • WS/T 535-2017 On-site rapid detection method for commonly used disinfectants in medical and health institutions

CZ-CSN, medical reagent

RO-ASRO, medical reagent

SE-SIS, medical reagent

  • SIS SS IEC 731:1988 Medical electrical equipment — Dos/meters with ionization chambers as used in radiotherapy

GOSTR, medical reagent

  • GOST 28518-1990 Medical chisels. General technical requirements and test methods

HU-MSZT, medical reagent

Professional Standard - Forestry, medical reagent

Canadian General Standards Board （CGSB), medical reagent

  • CGSB 2.161-97-CAN/CGSB-1997 Evaluation De L'Efficacite Des Agents Antimicrobiens Utilises Sur Des Surfaces Environnementales Et Sur Les Instruments Medicaux

IT-UNI, medical reagent

  • EC 1-2021 UNI EN 17126-2021 Chemical disinfectants and antiseptics - Quantitative suspension test for the evaluation of sporicidal activity of chemical disinfectants in the medical area - Test method and requirements (phase 2, step 1)
  • UNI EN 17387-2021 Chemical disinfectants and antiseptics - Quantitative test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants in the medical area on non-porous surfaces without mechanical action - Test method and requi

CU-NC, medical reagent

  • NC 21-02-1967 Aproximate concentration reagent solutions for general use
  • NC 21-03-1968 Exact concentration reagent solutions for general use

ASHRAE - American Society of Heating@ Refrigerating and Air-Conditioning Engineers@ Inc., medical reagent

Professional Standard - Agriculture, medical reagent

  • GB 603-1988 Preparation of preparations and products used in chemical reagent test methods
  • GB/T 603-2023 Preparation of preparations and products used in chemical reagent test methods

CH-SNV, medical reagent

  • SN EN 17387-2021 Chemical disinfectants and antiseptics - Quantitative test for the evaluation of bactericidal and yeasticidal and/or fungicidal activity of chemical disinfectants in the medical area on non-porous surfaces without mechanical action - Test method and requi

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

  • GB 15213-2016 Medical electron accelerators—Functional performance characteristics and test methods

Shanghai Provincial Standard of the People's Republic of China, medical reagent

  • DB31/ 351-2005 Technical specifications for safe use of skin and mucous membrane disinfectants for infants (including newborns) in hospitals

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