Withdrawn and superseded ISO standards — page 15 of 246

25333,IS,,ISO 10993-1:1997,Biological evaluation of medical devices — Part 1: Evaluation and testing,Évaluation biologique des dispositifs médicaux — Partie 1: Évaluation et essais,1997-12-11,2,['11.100'],ISO/TC 194,9599,"[18960,21225]","[36404,37875]","['en','fr']",12,

37875,IS,,ISO 10993-1:2003,Biological evaluation of medical devices — Part 1: Evaluation and testing,Évaluation biologique des dispositifs médicaux — Partie 1: Évaluation et essais,2003-07-28,3,['11.100.20'],ISO/TC 194,9599,[25333],[44908],"['en','fr']",14,"<p>ISO 10993-1:2003 describes</p><ol><li>the general principles governing the biological evaluation of medical devices;</li><li>the categorization of devices based on the nature and duration of their contact with the body;</li><li>the selection of appropriate tests.</li></ol><p>It does not cover testing of materials and devices that do not come into direct or indirect contact with the patient's body, nor does it cover biological hazards a

44908,IS,,ISO 10993-1:2009,Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process,Évaluation biologique des dispositifs médicaux — Partie 1: Évaluation et essais au sein d'un processus de gestion du risque,2009-10-13,4,['11.100.20'],ISO/TC 194,9599,[37875],[68936],"['en','fr']",21,<p>ISO 10993-1:2009 describes:</p><ul><li>the general principles governing the biological evaluation of medical devices within a risk management process;</li><li>the general categorization of devices based on the nature and duration of their contact with the body;</li><li>the evaluation of existing relevant data from all sources;</li><li>the identification of gaps

56669,IS,Cor,ISO 10993-1:2009/Cor 1:2010,Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process — Technical Corrigendum 1,Évaluation biologique des dispositifs médicaux — Partie 1: Évaluation et essais au sein d'un processus de gestion du risque — Rectificatif technique 1,2010-06-04,4,['11.100.20'],ISO/TC 194,9599,,[68936],"['en','fr']",1,

68936,IS,,ISO 10993-1:2018,Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process,Évaluation biologique des dispositifs médicaux — Partie 1: Évaluation et essais au sein d'un processus de gestion du risque,2018-08-17,5,['11.100.20'],ISO/TC 194,9599,"[44908,56669]",[84512],"['en','fr']",41,"<p>This document specifies:</p><p>— the general principles governing the biological evaluation of medical devices within a risk management process;</p><p>— the general categorization of medical devices based on the nature and duration of their contact with the body;</p><p>— the evaluation of existing relevant data from all sourc

18971,IS,,ISO 10993-10:1995,Biological evaluation of medical devices — Part 10: Tests for irritation and sensitization,Évaluation biologique des dispositifs médicaux — Partie 10: Essais d'irritation et de sensibilisation,1995-03-09,1,['11.100'],ISO/TC 194,9599,,[33364],"['en','fr']",31,<p>Describes test methods to evaluate the potential of devices and their constituent materials to produce irritation and to produce sensitization. Also gives guidance for the preparation of materials specifically in relation to the above tests.</p>

33364,IS,,ISO 10993-10:2002,Biological evaluation of medical devices — Part 10: Tests for irritation and delayed-type hypersensitivity,Évaluation biologique des dispositifs médicaux — Partie 10: Essais d'irritation et d'hypersensibilité retardée,2002-09-26,2,['11.100.20'],ISO/TC 194,9599,[18971],[40884],"['en','fr']",49,"<p>This part of ISO 10993 describes the procedure for the assessment of medical devices and their constituent materials with regard to their potential to produce irritation and delayed-type hypersensitivity.</p><p>This part of ISO 10993 includes pretest considerations, details of the test procedures, and key factors for the interpretation of the results.</p><p>Guidance is gi

39360,IS,Amd,ISO 10993-10:2002/Amd 1:2006,Biological evaluation of medical devices — Part 10: Tests for irritation and delayed-type hypersensitivity — Amendment 1,Évaluation biologique des dispositifs médicaux — Partie 10: Essais d'irritation et d'hypersensibilité retardée — Amendement 1,2006-07-06,2,['11.100.20'],ISO/TC 194,9599,,[40884],"['en','fr']",2,

40884,IS,,ISO 10993-10:2010,Biological evaluation of medical devices — Part 10: Tests for irritation and skin sensitization,Évaluation biologique des dispositifs médicaux — Partie 10: Essais d'irritation et de sensibilisation cutanée,2010-07-27,3,['11.100.20'],ISO/TC 194,9599,"[33364,39360]",[75279],"['en','fr']",67,"<p>ISO 10993-10:2010 describes the procedure for the assessment of medical devices and their constituent materials with regard to their potential to produce irritation and skin sensitization.</p><p>ISO 10993-10:2010 includes:</p><ul><li>pretest considerations for irritation, including <i>in silico</i> and <i>in vitro</i> methods for dermal exposure;</li><li>details of <i>in vivo

18972,IS,,ISO 10993-11:1993,Biological evaluation of medical devices — Part 11: Tests for systemic toxicity,Évaluation biologique des dispositifs médicaux — Partie 11: Essais de toxicité systémique,1993-12-09,1,['11.100.20'],ISO/TC 194,9599,,[35977],"['en','fr']",8,"<p>Specifies methodologies for the evaluation of the systemic toxicity potential of medical devices which release constituents into the body. Includes, in addition, pyrogenicity testing. The methods cited are from international standards, national standards, directives and regulations.</p>"

35977,IS,,ISO 10993-11:2006,Biological evaluation of medical devices — Part 11: Tests for systemic toxicity,Évaluation biologique des dispositifs médicaux — Partie 11: Essais de toxicité systémique,2006-08-15,2,['11.100.20'],ISO/TC 194,9599,[18972],[68426],"['en','fr']",26,<p>ISO 10993-11:2006 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.</p>

18973,IS,,ISO 10993-12:1996,Biological evaluation of medical devices — Part 12: Sample preparation and reference materials,Évaluation biologique des dispositifs médicaux — Partie 12: Préparation des échantillons et matériaux de référence,1996-09-05,1,['11.100'],ISO/TC 194,9599,,[35331],"['en','fr']",11,"<p>Specifies requirements and guidance on procedures to be followed in the preparation of samples of medical devices for testing in biological systems. Includes test material selection, selection of representative portions from a device and selection of reference materials to demonstrate the suitability of the test system.</p>"

35331,IS,,ISO 10993-12:2002,Biological evaluation of medical devices — Part 12: Sample preparation and reference materials,Évaluation biologique des dispositifs médicaux — Partie 12: Préparation des échantillons et matériaux de référence,2002-12-11,2,['11.100.20'],ISO/TC 194,9599,[18973],[40384],"['en','fr']",15,"<p>ISO 10993-12:2002 specifies requirements and gives guidance on the procedures to be followed in the preparation of samples and the selection of reference materials for medical devices testing in biological systems in accordance with one or more parts of the ISO 10993 series. </p><p>Specifically, ISO 10993-12:2002 addresses:</p><ul><li>test material selection;</li><li>selection of

40384,IS,,ISO 10993-12:2007,Biological evaluation of medical devices — Part 12: Sample preparation and reference materials,Évaluation biologique des dispositifs médicaux — Partie 12: Préparation des échantillons et matériaux de référence,2007-10-31,3,['11.100.20'],ISO/TC 194,9599,[35331],[53468],"['en','fr']",17,<p>ISO 10993-12:2007 specifies requirements and gives guidance on the procedures to be followed in the preparation of samples and the selection of reference materials for medical device testing in biological systems in accordance with one or more parts of the ISO 10993 series. Specifically ISO 10993-12:2007 addresses:</p><ol><li>test sample selection;</li><li>selection of representat

53468,IS,,ISO 10993-12:2012,Biological evaluation of medical devices — Part 12: Sample preparation and reference materials,Évaluation biologique des dispositifs médicaux — Partie 12: Préparation des échantillons et matériaux de référence,2012-06-29,4,['11.100.20'],ISO/TC 194,9599,[40384],[75769],"['en','fr','ru']",20,"<p>ISO 10993-12:2012 specifies requirements and gives guidance on the procedures to be followed in the preparation of samples and the selection of reference materials for medical device testing in biological systems in accordance with one or more parts of ISO 10993. Specifically, ISO 10993-12:2012 addresses the following:</p><ul><li>test sample selection;</li><li>selection of r

22692,IS,,ISO 10993-13:1998,Biological evaluation of medical devices — Part 13: Identification and quantification of degradation products from polymeric medical devices,Évaluation biologique des dispositifs médicaux — Partie 13: Identification et quantification de produits de dégradation de dispositifs médicaux à base de polymères,1998-11-19,1,['11.100.20'],ISO/TC 194,9599,,[44050],"['en','fr']",10,

22694,IS,,ISO 10993-15:2000,Biological evaluation of medical devices — Part 15: Identification and quantification of degradation products from metals and alloys,Évaluation biologique des dispositifs médicaux — Partie 15: Identification et quantification des produits de dégradation issus des métaux et alliages,2000-11-30,1,['11.100.20'],ISO/TC 194,9599,,[68937],"['en','fr']",12,

22695,IS,,ISO 10993-16:1997,Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables,Évaluation biologique des dispositifs médicaux — Partie 16: Conception des études toxicocinétiques des produits de dégradation et des substances relargables,1997-08-28,1,['11.100.20'],ISO/TC 194,9599,,[45367],"['en','fr']",9,

45367,IS,,ISO 10993-16:2010,Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables,Évaluation biologique des dispositifs médicaux — Partie 16: Conception des études toxicocinétiques des produits de dégradation et des substances relargables,2010-02-09,2,['11.100.20'],ISO/TC 194,9599,[22695],[64582],"['en','fr']",11,<p>ISO 10993-16:2010 gives principles on how toxicokinetic studies relevant to medical devices should be designed and performed. Annex A describes the considerations for inclusion of toxicokinetic studies in the biological evaluation of medical devices.</p>

23955,IS,,ISO 10993-17:2002,Biological evaluation of medical devices — Part 17: Establishment of allowable limits for leachable substances,Évaluation biologique des dispositifs médicaux — Partie 17: Établissement des limites admissibles des substances relargables,2002-11-27,1,['11.100.20'],ISO/TC 194,9599,,"[75323,64744]","['en','fr']",25,"<p>ISO 10993-17:2002 specifies the determination of allowable limits for substances leachable from medical devices. It is intended for use in deriving standards and estimating appropriate limits where standards do not exist. It describes a systematic process through which identified risks arising from toxicologically hazardous substances present in medical

41106,IS,,ISO 10993-18:2005,Biological evaluation of medical devices — Part 18: Chemical characterization of materials,Évaluation biologique des dispositifs médicaux — Partie 18: Caractérisation chimique des matériaux,2005-06-30,1,['11.100.20'],ISO/TC 194,9599,,[64750],"['en','fr','ru']",17,"<p>ISO 10993-18:2005 describes a framework for the identification of a material and the identification and quantification of its chemical constituents. The chemical characterization information generated can be used for a range of important applications, for example, as part of an assessment of the overall biological safety of a medical device (ISO 10993-1 and 14971), as a measurement of the level of a l

18961,IS,,ISO 10993-2:1992,Biological evaluation of medical devices — Part 2: Animal welfare requirements,Évaluation biologique des dispositifs médicaux — Partie 2: Exigences concernant la protection des animaux,1992-12-30,1,['11.100.20'],ISO/TC 194,9599,,[36405],"['en','fr']",5,"<p>Specifies minimum requirements for the use of animals in biological testing. Is also intended to establish guidelines which allow the scientist to respect life in general, to reduce the number of animal experiments and the number of animals used in experiments, to minimize suffering and maintain the quality of life of the animals used in the experiments. Applies to the experimentation performed on vertebrates.</p

36405,IS,,ISO 10993-2:2006,Biological evaluation of medical devices — Part 2: Animal welfare requirements,Évaluation biologique des dispositifs médicaux — Partie 2: Exigences relatives à la protection des animaux,2006-07-06,2,['11.100.20'],ISO/TC 194,9599,[18961],[78866],"['en','fr']",13,"<p>ISO 10993-2:2006 is aimed at those who commission, design and perform tests or evaluate data from animal tests undertaken to assess the biocompatibility of materials intended for use in medical devices, or of the medical devices themselves. It specifies the minimum requirements to be satisfied to ensure and demonstrate that proper provision has been made for the welfare of animals used in animal tests to

18962,IS,,ISO 10993-3:1992,"Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity","Évaluation biologique des dispositifs médicaux — Partie 3: Essais concernant la génotoxicité, la cancérogénicité et la toxicité sur la reproduction",1992-12-30,1,['11.100'],ISO/TC 194,9599,,[32162],"['en','fr']",7,"<p>Most tests specified refer to the OECD guidelines for testing of chemicals. At the time of testing, these tests are to be performed according to current OECD guidelines. Guidance on selection of tests is provided in ISO 10993-1.</p>"

32162,IS,,ISO 10993-3:2003,"Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity","Évaluation biologique des dispositifs médicaux — Partie 3: Essais concernant la génotoxicité, la cancérogénicité et la toxicité sur la reproduction",2003-10-22,2,['11.100.20'],ISO/TC 194,9599,[18962],[55614],"['en','fr']",16,"<p>ISO 10993-3:2003 specifies strategies for hazard identification and tests on medical devices for the following biological aspects: genotoxicity, carcinogenicity, and reproductive and developmental toxicity.</p><p>ISO 10993-3:2003 is applicable for evaluation of a medical device whose potential for genotoxicity, carcinogeni

18963,IS,,ISO 10993-4:1992,Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood,Évaluation biologique des dispositifs médicaux — Partie 4: Choix des essais concernant les interactions avec le sang,1992-12-30,1,['11.100'],ISO/TC 194,9599,,[32086],"['en','fr']",19,"<p>Describes a classification of medical and dental devices that are intended for use in contact with blood, the fundamental principles governing the evaluation of the interaction of devices with blood, and the rationale for structured selection of tests, together with the principles and scientific basis of these tests. Annex A describes evaluation of cardiovascular devices and prostheses

32086,IS,,ISO 10993-4:2002,Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood,Évaluation biologique des dispositifs médicaux — Partie 4: Choix des essais pour les interactions avec le sang,2002-10-22,2,['11.100.20'],ISO/TC 194,9599,[18963],"[50994,63448]","['en','fr']",34,"<p>ISO 10993-4:2002 provides general requirements for evaluating the interactions of medical devices with blood.</p><p>It describes</p><ol><li>a classification of medical and dental devices that are intended for use in contact with blood, based on the intended use and duration of contact as defined in ISO 10993-1,</li><li>the fundamental principles governing the evaluation of

39205,IS,Amd,ISO 10993-4:2002/Amd 1:2006,Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood — Amendment 1,Évaluation biologique des dispositifs médicaux — Partie 4: Choix des essais pour les interactions avec le sang — Amendement 1,2006-07-21,2,['11.100.20'],ISO/TC 194,9599,,"[50994,63448]","['en','fr']",5,

18964,IS,,ISO 10993-5:1992,Biological evaluation of medical devices — Part 5: Tests for cytotoxicity: in vitro methods,Évaluation biologique des dispositifs médicaux — Partie 5: Essais de cytotoxicité: méthodes in vitro,1992-12-30,1,['11.100'],ISO/TC 194,9599,,[26211],"['en','fr']",7,

26211,IS,,ISO 10993-5:1999,Biological evaluation of medical devices — Part 5: Tests for in vitro cytotoxicity,Évaluation biologique des dispositifs médicaux — Partie 5: Essais concernant la cytotoxicité in vitro,1999-05-20,2,['11.100.20'],ISO/TC 194,9599,[18964],[36406],"['en','fr']",8,

18966,IS,,ISO 10993-6:1994,Biological evaluation of medical devices — Part 6: Tests for local effects after implantation,Évaluation biologique des dispositifs médicaux — Partie 6: Essais concernant les effets locaux après implantation,1994-07-07,1,['11.100.20'],ISO/TC 194,9599,,[44789],"['en','fr']",11,"<p>Specifies test methods for the assessment of the local effects of an implant material on living tissue, at both the macroscopic and microscopic level. The local effects are evaluated by a comparison of the tissue response caused by a test specimen to that caused by materials used in medical devices whose clinical acceptability has been established. The test methods for local effects after

44789,IS,,ISO 10993-6:2007,Biological evaluation of medical devices — Part 6: Tests for local effects after implantation,Évaluation biologique des dispositifs médicaux — Partie 6: Essais concernant les effets locaux après implantation,2007-04-04,2,['11.100.20'],ISO/TC 194,9599,[18966],[61089],"['en','fr']",21,"<p>ISO 10993-6:2007 specifies test methods for the assessment of the local effects after implantation of biomaterials intended for use in medical devices.</p><p>ISO 10993-6:2007 applies to materials that are:</p><ol><li>solid and non-biodegradable;</li><li>degradable and/or resorbable;</li><li>non-solid, such as porous materials, liquids, pastes and particulates.</li></ol><p>ISO 10993-

61089,IS,,ISO 10993-6:2016,Biological evaluation of medical devices — Part 6: Tests for local effects after implantation,Évaluation biologique des dispositifs médicaux — Partie 6: Essais concernant les effets locaux après implantation,2016-11-28,3,['11.100.20'],ISO/TC 194,9599,[44789],[83976],"['en','fr']",29,"<p>ISO 10993-6:2016 specifies test methods for the assessment of the local effects after implantation of biomaterials intended for use in medical devices.</p><p>ISO 10993-6:2016 applies to materials that are</p><p>- solid and non-absorbable,</p><p>- non-solid, such as porous materials, liquids, gels, pastes, and particulates, and</p><p>- degradable and/or absorbable, whi

18967,IS,,ISO 10993-7:1995,Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals,Évaluation biologique des dispositifs médicaux — Partie 7: Résidus de stérilisation à l'oxyde d'éthylène,1995-10-12,1,['11.100.20'],ISO/TC 194,9599,,[34213],"['en','fr']",40,<p>Specifies allowable limits for residual ethylene oxide (EO) and ethylene chlorohydrin (ECH) in individual EO-sterilized medical devices and procedures for the measurement of EO and ECH. Does not apply for EO-sterilized devices that have no patient contact such as in vitro diagnostic devices.</p>

34213,IS,,ISO 10993-7:2008,Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals,Évaluation biologique des dispositifs médicaux — Partie 7: Résidus de stérilisation à l'oxyde d'éthylène,2008-10-13,2,['11.100.20'],ISO/TC 194,9599,[18967],[84824],"['en','fr']",86,"<p>ISO 10993-7:2008 specifies allowable limits for residual ethylene oxide (EO) and ethylene chlorohydrin (ECH) in individual EO-sterilized medical devices, procedures for the measurement of EO and ECH, and methods for determining compliance so that devices may be released. Additional background, including guidance and a flowchart showing how the standard is applied are also included in informative

72766,IS,Amd,ISO 10993-7:2008/Amd 1:2019,Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Amendment 1: Applicability of allowable limits for neonates and infants,Évaluation biologique des dispositifs médicaux — Partie 7: Résidus de stérilisation à l'oxyde d'éthylène — Amendement 1: titre manque,2019-12-09,2,['11.100.20'],ISO/TC 194,9599,,[84824],"['en','fr']",5,

55064,IS,Cor,ISO 10993-7:2008/Cor 1:2009,Biological evaluation of medical devices — Part 7: Ethylene oxide sterilization residuals — Technical Corrigendum 1,Évaluation biologique des dispositifs médicaux — Partie 7: Résidus de stérilisation à l'oxyde d'éthylène — Rectificatif technique 1,2009-11-12,2,['11.100.20'],ISO/TC 194,9599,,[84824],"['en','fr']",2,

26212,IS,,ISO 10993-9:1999,Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products,Évaluation biologique des dispositifs médicaux — Partie 9: Cadre pour l'identification et la quantification des produits potentiels de dégradation,1999-03-04,1,['11.100.20'],ISO/TC 194,9599,[18970],[44049],"['en','fr']",8,

44049,IS,,ISO 10993-9:2009,Biological evaluation of medical devices — Part 9: Framework for identification and quantification of potential degradation products,Évaluation biologique des dispositifs médicaux — Partie 9: Cadre pour l'identification et la quantification des produits potentiels de dégradation,2009-11-30,2,['11.100.20'],ISO/TC 194,9599,[26212],[64580],"['en','fr']",9,<p>ISO 10993-9:2008 provides general principles for the systematic evaluation of the potential and observed biodegradation of medical devices and for the design and performance of biodegradation studies. Information obtained from these studies can be used in the biological evaluation described in the ISO 10993 series

18978,IS,,ISO 10998:1995,Agricultural wheeled tractors — Steering requirements,Tracteurs agricoles à roues — Exigences relatives à la conduite,1995-11-23,1,['65.060.10'],ISO/TC 23/SC 2,9599,,[43556],"['en','fr']",3,<p>Specifies performance requirements for normal and emergency steering modes for agricultural wheeled tractors having at least two axles fitted with pneumatic tyres. Does not apply to track-type or skid-steered agricultural tractors.</p>

3591,IS,,ISO 11:1980,Aircraft — Pressure cabin ground test connections,Aéronefs — Raccord pour essai au sol de pressurisation de la cabine des aéronefs,1980-03-01,1,"['49.100','49.080']",ISO/TC 20/SC 10,9599,,[3592],"['en','fr']",2,

5610,IS,,ISO 1100-1:1981,Liquid flow measurement in open channels — Part 1: Establishment and operation of a gauging station,Mesure de débit des liquides dans les canaux découverts — Partie 1: Établissement et exploitation d'une station de jaugeage,1981-10-01,1,['17.120.20'],ISO/TC 113,9599,[5609],[5611],"['en','fr']",21,

5611,IS,,ISO 1100-1:1996,Measurement of liquid flow in open channels — Part 1: Establishment and operation of a gauging station,Mesurage de débit des liquides dans les canaux découverts — Partie 1: Établissement et exploitation d'une station hydrométrique,1996-02-08,2,['17.120.20'],ISO/TC 113/SC 1,9599,[5610],"[53942,62267]",['en'],20,"<p>Deals with the establishment and operation of a gauging station for the measurement of stage oder discharge, or both, of a lake, reservoir, river or artificial open channel. Replaces the first edition.</p>"

5609,IS,,ISO 1100:1973,Withdrawal of ISO 1100-1973,Annulation de l'ISO 1100-1973,1973-12-01,1,['17.120.20'],ISO/TC 113,9599,,"[5610,5612]","['en','fr']",29,

5612,IS,,ISO 1100-2:1982,Liquid flow measurement in open channels — Part 2: Determination of the stage-discharge relation,Mesure de débit des liquides dans les canaux découverts — Partie 2: Détermination de la relation hauteur-débit,1982-06-01,1,['17.120.20'],ISO/TC 113/SC 2,9599,[5609],[5613],"['en','fr']",33,

5613,IS,,ISO 1100-2:1998,Measurement of liquid flow in open channels — Part 2: Determination of the stage-discharge relation,Mesurage de débit des liquides dans les canaux découverts — Partie 2: Détermination de la relation hauteur-débit,1998-05-07,2,['17.120.20'],ISO/TC 113/SC 1,9599,[5612],[42207],['en'],25,

34341,IS,Cor,ISO 1100-2:1998/Cor 1:2000,Measurement of liquid flow in open channels — Part 2: Determination of the stage-discharge relation — Technical Corrigendum 1,Mesurage de débit des liquides dans les canaux découverts — Partie 2: Détermination de la relation hauteur-débit — Rectificatif technique 1,2000-08-17,2,['17.120.20'],ISO/TC 113/SC 1,9599,,[42207],['en'],2,

42207,IS,,ISO 1100-2:2010,Hydrometry — Measurement of liquid flow in open channels — Part 2: Determination of the stage-discharge relationship,Hydrométrie — Mesurage du débit des liquides dans les canaux découverts — Partie 2: Détermination de la relation hauteur-débit,2010-11-15,3,['17.120.20'],ISO/TC 113/SC 1,9599,"[34341,5613]",[62154],['en'],28,"<p>ISO 1100-2:2010 specifies methods of determining the stage-discharge relationship for a gauging station. A sufficient number of discharge measurements, complete with corresponding stage measurements, are required to define a stage-discharge relationship to the accuracy required by ISO 1100-2.</p><p>Stable and unstable channels are considered,

18981,IS,,ISO 11001-1:1993,Agricultural wheeled tractors and implements — Three-point hitch couplers — Part 1: U-frame coupler,Tracteurs agricoles à roues et instruments — Coupleurs rapides trois points — Partie 1: Coupleur par cadre en U,1993-09-30,1,['65.060.01'],ISO/TC 23/SC 4,9599,,[60879],"['en','fr']",4,"<p>Specifies the essential dimensions for the attachment of three-point hitch implements to agricultural wheeled tractors equipped with a three-point free link hitch according to ISO 730-1, ISO 730-3 or ISO 8759-2, and a U-frame hitch coupler. The three-point hitch coupler systems constitute a special method of implement mounting. The hitch couplers are an additional component located

18983,IS,,ISO 11001-3:1993,Agricultural wheeled tractors and implements — Three-point hitch couplers — Part 3: Link coupler,Tracteurs agricoles à roues et instruments — Coupleurs rapides trois points — Partie 3: Coupleur à rotules,1993-09-30,1,['65.060.01'],ISO/TC 23/SC 4,9599,,[42848],"['en','fr']",2,"<p>Specifies the essential dimensions for the attachment of three-point hitch implements to agricultural wheeled tractors equipped with a three-point free link hitch according to ISO 730-1 or ISO 8759-2, and a set of link couplers. The three-point hitch coupler systems constitute a special method of implement mounting. The hitch couplers are an additional component located between the three-po

18986,IS,,ISO 11003-1:1993,Adhesives — Determination of shear behaviour of structural bonds — Part 1: Torsion test method using butt-bonded hollow cylinders,Adhésifs — Détermination du comportement en cisaillement de joints structuraux — Partie 1: Méthode d'essai en torsion de cylindres creux collés bout à bout,1993-09-09,1,['83.180'],ISO/TC 61/SC 11,9599,,[31289],"['en','fr']",7,"<p>The principle of the method specified is determining the deformation of the adhesive in the annular bond between two butt-jointed hollow cylinders as a function of the applied torque up to failure of the joint. The circular symmetry of the specimen entails a state of simple shear with uniform strain in the bond

31289,IS,,ISO 11003-1:2001,Adhesives — Determination of shear behaviour of structural adhesives — Part 1: Torsion test method using butt-bonded hollow cylinders,Adhésifs — Détermination du comportement en cisaillement d'adhésifs structuraux — Partie 1: Méthode d'essai en torsion de cylindres creux collés bout à bout,2001-12-20,2,['83.180'],ISO/TC 61/SC 11,9599,[18986],[75589],"['en','fr']",9,

18987,IS,,ISO 11003-2:1993,Adhesives — Determination of shear behaviour of structural bonds — Part 2: Thick-adherend tensile-test method,Adhésifs — Détermination du comportement en cisaillement de joints structuraux — Partie 2: Méthode d'essai en traction sur éprouvette épaisse,1993-09-09,1,['83.180'],ISO/TC 61/SC 11,9599,,[30095],"['en','fr']",12,"<p>The test is performed on specimens consisting of thick, rigid adherends, with a short length of overlap, in order to obtain the most uniform distribution of shear stresses possible and to minimize undesired stresses. The method may be used to determine the shear properties of an adhesive (stress and strain), the shear modulus of the adhesive, a

30095,IS,,ISO 11003-2:2001,Adhesives — Determination of shear behaviour of structural adhesives — Part 2: Tensile test method using thick adherends,Adhésifs — Détermination du comportement en cisaillement d'adhésifs structuraux — Partie 2: Méthode d'essai en traction sur éprouvette épaisse,2001-12-20,2,['83.180'],ISO/TC 61/SC 11,9599,[18987],[75590],"['en','fr']",14,

18991,IS,,ISO 11007:1997,Petroleum products and lubricants — Determination of rust-prevention characteristics of lubricating greases,Produits pétroliers et lubrifiants — Détermination des caractéristiques antirouille des graisses lubrifiantes,1997-06-26,1,['75.100'],ISO/TC 28,9599,,"[79196,79197]","['en','fr']",7,<p>This International Standard specifies a method for the determination of the rust-prevention characteristics of lubricating grease in the presence of an aqueous test fluid.</p>

32504,IS,,ISO 11009:2000,Petroleum products and lubricants — Determination of water washout characteristics of lubricating greases,Produits pétroliers et lubrifiants — Détermination de la résistance au délavage à l'eau des graisses lubrifiantes,2000-03-09,1,['75.100'],ISO/TC 28,9599,,[78960],"['en','fr']",7,"<p>This International Standard specifies a method for evaluating the resistance of a lubricating grease to washout by</p><p>water from a bearing, when tested at 38 °C and 79 °C under specified laboratory conditions.</p><p>It is not to be considered the equivalent of service evaluation tests.</p>"

5614,IS,,ISO 1101:1983,"Technical drawings — Geometrical tolerancing — Tolerancing of form, orientation, location and run-out — Generalities, definitions, symbols, indications on drawings","Dessins techniques — Tolérancement géométrique — Tolérancement de forme, orientation, position et battement — Généralités, définitions, symboles, indications sur les dessins",1983-12-01,1,['01.100.20'],ISO/TC 213,9599,[5616],[1147],"['en','fr']",24,"<p>The document forms an axtract of ISO 1101, suitable for e

5617,IS,,ISO 1101-2:1974,Technical drawings — Tolerances of form and of position — Part 2: Maximum material principle,Dessins techniques — Tolérances de forme et tolérances de position — Partie 2: Principe du maximum de matière,1974-05-01,1,['01.100.20'],ISO/TC 10,9599,,[7653],"['en','fr']",7,

1147,IS,,ISO 1101:2004,"Geometrical Product Specifications (GPS) — Geometrical tolerancing — Tolerances of form, orientation, location and run-out","Spécification géométrique des produits (GPS) — Tolérancement géométrique — Tolérancement de forme, orientation, position et battement",2004-12-09,2,"['17.040.10','01.100.20']",ISO/TC 213,9599,[5614],[59490],"['en','fr']",54,<p>ISO 1101:2004 contains basic information and gives requirements for the geometrical tolerancing of workpieces.</p>

59490,IS,,ISO 1101:2012,"Geometrical product specifications (GPS) — Geometrical tolerancing — Tolerances of form, orientation, location and run-out","Spécification géométrique des produits (GPS) — Tolérancement géométrique — Tolérancement de forme, orientation, position et battement",2012-04-23,3,"['17.040.10','01.100.20']",ISO/TC 213,9599,"[18662,1147,45974]",[66777],"['en','fr','ru']",103,<p>ISO 1101:2012 contains basic information and gives requirements for the geometrical tolerancing of work

63512,IS,Cor,ISO 1101:2012/Cor 1:2013,"Geometrical product specifications (GPS) — Geometrical tolerancing — Tolerances of form, orientation, location and run-out — Technical Corrigendum 1","Spécification géométrique des produits (GPS) — Tolérancement géométrique — Tolérancement de forme, orientation, position et battement — Rectificatif technique 1",2013-02-04,3,"['17.040.10','01.100.20']",ISO/TC 213,9599,,[66777],"['en','fr','ru']",2,

18998,IS,,ISO 11014-1:1994,Safety data sheet for chemical products — Part 1: Content and order of sections,Fiches de données de sécurité pour les produits chimiques — Partie 1: Contenu et plan type,1994-03-10,1,['71.100.01'],ISO/TC 47,9599,,"[44690,37086]","['en','fr']",7,"<p>Presents information for the compilation and completion of a safety data sheet. Defines specifically the general layout of the SDS, the 16 standard headings, the numbering and the sequence of these 16 standard headings, the items necessary to fill in an SDS and the conditions of their applicability or utilization.</p>"

5618,IS,,ISO 1102:1975,Road vehicles — Mechanical connections between towing vehicles and trailers — Interchangeability,Véhicules routiers — Liaisons mécaniques entre véhicules tracteurs et remorques — Interchangeabilité,1975-03-01,1,['43.040.70'],ISO/TC 22,9599,,[5619],"['en','fr']",3,

5619,IS,,ISO 1102:1986,Commercial road vehicles — Mechanical connections between towing vehicles and trailers — 50 mm drawbar couplings,Véhicules routiers utilitaires — Liaisons mécaniques entre véhicules tracteurs et remorques — Dispositifs d'attelage de 50 mm,1986-12-18,2,['43.040.70'],ISO/TC 22,9599,[5618],"[30354,20557]","['en','fr']",5,"<p>This second edition cancels and replaces the first edition (1975). Specifies the essential dimensions of a 50 mm drawbar coupling and a 50 mm drawbar eye to permit interchangeability. Applies to mechanical connections designed for commercial vehicles and trailers, the maximum total mass of which is above 3,5 t.</p>"

19011,IS,,ISO 11027:1993,Pepper and pepper oleoresins — Determination of piperine content — Method using high-performance liquid chromatography,"Poivres, oléorésines de poivres — Détermination de la teneur en pipérine — Méthode par chromatographie en phase liquide à haute performance",1993-07-08,1,['67.220.10'],ISO/TC 34/SC 7,9599,,[90589],"['en','fr']",5,"<p>Specifies a method for the determination (by high-performance liquid chromatography) of the piperine content of ground pepper, whole pepper and oleoresins of pepper. The method enables a separation and, if necessary, the determination of the other alkaloids of pepper (isochavicine, isopiperine and piperittin).</p>"

5620,IS,,ISO 1103:1976,Road vehicles — Caravans and light trailers — Coupling ball — Dimensional characteristics,Véhicules routiers — Caravanes et remorques légères — Boule d'attelage — Caractéristiques dimensionnelles,1976-09-01,2,['43.040.70'],ISO/TC 22,9599,,[1099],"['en','fr']",2,

1099,IS,,ISO 1103:1996,Road vehicles — Coupling balls for caravans and light trailers — Dimensions,Véhicules routiers — Boules d'attelage pour caravanes et remorques légères — Caractéristiques dimensionnelles,1996-02-29,3,['43.040.70'],ISO/TC 22,9599,[5620],[40254],"['en','fr']",6,<p>Prescribes the dimensions necessary for the compatibility of mechanical coupling devices between light trailers or caravans and towing vehicles when the latter are fitted with a coupling ball. Replaces the second edition.</p>

19016,IS,,ISO 11036:1994,Sensory analysis — Methodology — Texture profile,Analyse sensorielle — Méthodologie — Profil de la texture,1994-11-24,1,['67.240'],ISO/TC 34/SC 12,9599,,"[76668,58038]","['en','fr']",14,<p>Describes a method of developing a texture profile of food products or non-food products. This method is just one approach to sensory texture profile analysis. Other methods exist. It describes various steps in the process of establishing a complete description of the textural attributes of a product.</p>

19017,IS,,ISO 11037:1999,Sensory analysis — General guidance and test method for assessment of the colour of foods,Analyse sensorielle — Directives générales et méthode d'essai pour l'évaluation de la couleur des produits alimentaires,1999-08-12,1,['67.240'],ISO/TC 34/SC 12,9599,,[50112],"['en','fr']",11,

19020,IS,,ISO 11040-1:1992,Prefilled syringes — Part 1: Glass cylinders for dental local anaesthetic cartridges,Seringues préremplies — Partie 1: Tubes en verre pour cartouches dentaires d'anesthésie locale,1992-11-19,1,"['11.040.10','11.040.25','11.060.20']",ISO/TC 76,9599,,[67064],"['en','fr']",3,"<p>Specifies the design, dimensions, materials, performance and test methods. Applies to primary packs used in direct contact with the drug.</p>"

20099,IS,,ISO 11040-2:1994,Prefilled syringes — Part 2: Plungers and discs for dental local anaesthetic cartridges,Seringues préremplies — Partie 2: Bouchons-pistons et rondelles d'étanchéité pour cartouches dentaires d'anesthésie locale,1994-12-22,1,"['11.040.10','11.040.25','11.060.20']",ISO/TC 76,9599,,[53947],"['en','fr']",9,"<p>Specifies the design, dimensions, materials, performance, requirements, marking and test methods for plungers and discs for dental local anaesthetic cartridges intended for single use only. Applies to primary packs used in direct contact with the drug.</p>"

19981,IS,,ISO 11040-3:1993,Prefilled syringes — Part 3: Aluminium caps for dental local anaesthetic cartridges,Seringues préremplies — Partie 3: Capsules en aluminium pour cartouches dentaires d'anesthésie locale,1993-03-25,1,"['11.040.10','11.040.25','11.060.20']",ISO/TC 76,9599,,[53948],"['en','fr']",2,"<p>Specifies the design, dimensions, material, performance requirements, packaging and marking of aluminium or aluminium alloy caps. Applies to primary packs used in direct contact with the drug.</p>"

53948,IS,,ISO 11040-3:2012,Prefilled syringes — Part 3: Seals for dental local anaesthetic cartridges,Seringues préremplies — Partie 3: Rondelles d'étanchéité pour cartouches dentaires d'anesthésie locale,2012-01-20,2,"['11.040.10','11.040.25','11.060.20']",ISO/TC 76,9599,[19981],[86875],"['en','fr']",6,"<p>ISO 11040-3:2012 specifies the shape, dimensions, material, performance requirements and labelling of seals for dental local anaesthetic cartridges intended for single use only.</p>"

21554,IS,,ISO 11040-4:1996,Prefilled syringes — Part 4: Glass barrels for injectables,Seringues préremplies — Partie 4: Cylindres en verre pour produits injectables,1996-04-18,1,['11.040.25'],ISO/TC 76,9599,,[43323],"['en','fr']",4,"<p>Applies to tubing-glass barrels (single-chamber design) for injection preparations and specifies materials, dimensions and performance details.</p>"

43323,IS,,ISO 11040-4:2007,Prefilled syringes — Part 4: Glass barrels for injectables,Seringues préremplies — Partie 4: Cylindres en verre pour produits injectables,2007-01-15,2,['11.040.25'],ISO/TC 76,9599,[21554],[58079],['en'],9,"<p>ISO 11040-4:2007 applies to tubing-glass barrels (single-chamber design) for injection preparations and specifies materials, dimensions and performance details.</p><p>Glass barrels from tubing glass in accordance with ISO 11040-4:2007 are intended for single use only. In conjunction with the right sealing components, they offer a safe system for parenteral use.</p>"

58079,IS,,ISO 11040-4:2015,Prefilled syringes — Part 4: Glass barrels for injectables and sterilized subassembled syringes ready for filling,Seringues préremplies — Partie 4: Cylindres en verre pour produits injectables et seringues pré-assemblées stérilisées préremplissables,2015-04-02,3,['11.040.25'],ISO/TC 76,9599,[43323],[82222],"['en','fr']",52,"<p>ISO 11040-4:2015 applies to</p><ul><li>tubing-glass barrels (single-chamber design) for injection preparations, and</li><li>sterilized subassembled syringes ready for filling.</li></ul><p>It specifies materials, dimensions, quality, and performance requirements, as well as relevant test methods.</p><p>ISO 11040-4:2015 also specifies those com

76777,IS,Amd,ISO 11040-4:2015/Amd 1:2020,Prefilled syringes — Part 4: Glass barrels for injectables and sterilized subassembled syringes ready for filling — Amendment 1,Seringues préremplies — Partie 4: Cylindres en verre pour produits injectables et seringues pré-assemblées stérilisées préremplissables — Amendement 1,2020-02-28,3,['11.040.25'],ISO/TC 76,9599,,[82222],"['en','fr']",3,

21555,IS,,ISO 11040-5:1996,Prefilled syringes — Part 5: Plungers for injectables,Seringues préremplies — Partie 5: Bouchons-pistons pour produits injectables,1996-04-18,1,['11.040.25'],ISO/TC 76,9599,,[33503],"['en','fr']",3,"<p>Applies to plungers for glass barrels (single-chamber design) for injection preparations in accordance with ISO 11040-4 and specifies materials, dimensions and performance details.</p>"

33503,IS,,ISO 11040-5:2001,Prefilled syringes — Part 5: Plungers for injectables,Seringues préremplies — Partie 5: Bouchons-pistons pour produits injectables,2001-12-20,2,['11.040.25'],ISO/TC 76,9599,[21555],[53968],"['en','fr']",4,

51919,IS,,ISO 11040-6:2012,Prefilled syringes — Part 6: Plastic barrels for injectables,Seringues préremplies — Partie 6: Cylindres en plastique pour produits injectables,2012-03-29,1,['11.040.25'],ISO/TC 76,9599,,[69487],"['en','fr']",10,

59937,IS,,ISO 11040-7:2015,Prefilled syringes — Part 7: Packaging systems for sterilized subassembled syringes ready for filling,Seringues préremplies — Partie 7: Systèmes d'emballage pour les seringues stérilisées prêtes à l'emploi préremplissables,2015-04-02,1,['11.040.25'],ISO/TC 76,9599,,[82921],"['en','fr']",27,"<p>ISO 11040-7:2015 specifies the packaging system that is used to deliver sterilized subassembled syringes ready for filling in tubs and nests.</p><p>Downstream processes (processes after filling such as in house/outside transport, reprocessing) can result in specific requirements on the packaging system used to deliver sterilized subassembled syringes ready for filling. Howeve

66036,IS,,ISO 11040-8:2016,Prefilled syringes — Part 8: Requirements and test methods for finished prefilled syringes,Seringues préremplies — Partie 8: Exigences et méthodes d'essai pour seringues préremplies prêtes à l'emploi,2016-11-04,1,['11.040.25'],ISO/TC 76,9599,,[85862],"['en','fr']",9,"<p>ISO 11040-8:2016 is applicable to aseptically filled or terminally sterilized finished prefilled syringes (intended for single use only) based on ISO 11040‑4 or ISO 11040‑6, together with ISO 11040‑5, for parenteral injection preparations with focus on quality, functional performance and safety requirements, as well as relevant test methods.</p><p>Finished prefilled syringes which have undergone an

19030,IS,,ISO 11050:1993,Wheat flour and durum wheat semolina — Determination of impurities of animal origin,Farines de blé tendre et semoules de blé dur — Détermination des impuretés d'origine animale,1993-07-01,1,['67.060'],ISO/TC 34/SC 4,9599,,[70014],"['en','fr']",11,"<p>The principle of the method described is hydrolysis of a test portion with a solution of hydrochloric acid at boiling point, concentration of the insoluble particles at a water/hydrocarbon interface, separation by filtration on a filter paper or membrane, microscopic examination, and counting under reflected light, of the impurities of animal origin (i.e. insects at all stages of their development, insect fragments, mite

19033,IS,,ISO 11054:1993,Cutting tools — Designation of high-speed steel groups,Outils coupants — Désignation des groupes d'aciers rapides,1993-12-02,1,"['77.140.35','25.100.01']",ISO/TC 29/SC 9,9599,,"[38556,38557]","['en','fr']",1,"<p>Specifies the designation of the groups HSS and HSS-E of high-speed steels used for manufacturing cutting tools such as taps, drills, etc. Is not intended to specify the composition of high-speed steels, which is stated in ISO 4957.</p>"

32338,IS,,ISO 11056:1999,Sensory analysis — Methodology — Magnitude estimation method,Analyse sensorielle — Méthodologie — Méthode d'estimation de la grandeur,1999-12-16,1,['67.240'],ISO/TC 34/SC 12,9599,,[72863],"['en','fr']",20,

58034,IS,Amd,ISO 11056:1999/Amd 1:2013,Sensory analysis — Methodology — Magnitude estimation method — Amendment 1,Analyse sensorielle — Méthodologie — Méthode d'estimation de la grandeur — Amendement 1,2013-02-18,1,['67.240'],ISO/TC 34/SC 12,9599,,[72863],"['en','fr']",1,

65520,IS,Amd,ISO 11056:1999/Amd 2:2015,Sensory analysis — Methodology — Magnitude estimation method — Amendment 2,Analyse sensorielle — Méthodologie — Méthode d'estimation de la grandeur — Amendement 2,2015-03-16,1,['67.240'],ISO/TC 34/SC 12,9599,,[72863],"['en','fr']",1,

19036,IS,,ISO 11058:1999,"Geotextiles and geotextile-related products — Determination of water permeability characteristics normal to the plane, without load","Géotextiles et produits apparentés — Détermination des caractéristiques de perméabilité à l'eau normalement au plan, sans contrainte mécanique",1999-03-04,1,['59.080.70'],ISO/TC 221,9599,,[54545],"['en','fr']",18,

54545,IS,,ISO 11058:2010,"Geotextiles and geotextile-related products — Determination of water permeability characteristics normal to the plane, without load","Géotextiles et produits apparentés — Détermination des caractéristiques de perméabilité à l'eau normalement au plan, sans contrainte mécanique",2010-03-25,2,['59.080.70'],ISO/TC 221,9599,"[19036,44161]",[70845],"['en','fr']",17,<p>ISO 11058:2010 specifies two test methods for determining the water permeability characteristics of a single layer of geotextile or geotextile-related product normal to the plane: </p><p>- the constant head method; </p><p>- the falling head method.</p>

5624,IS,,ISO 1106-1:1984,Recommended practice for radiographic examination of fusion welded joints — Part 1: Fusion welded butt joints in steel plates up to 50 mm thick,Pratique recommandée pour l'examen radiographique de joints soudés par fusion — Partie 1: Joints soudés bout à bout par fusion de tôles d'acier d'épaisseur inférieure à 50 mm,1984-12-01,1,['25.160.40'],ISO/TC 44/SC 5,9599,[5623],[29970],"['en','fr']",8,<p>The detection of flaws in an item submitted to X- or gamma-radiographic examination depends on the particularities of the technique employed. This part of ISO 1106 specifies general techniques of weld radiography with the object of enabling satisfactory results to be obtaine

5625,IS,,ISO 1106-2:1985,Recommended practice for radiographic examination of fusion welded joints — Part 2: Fusion welded butt joints in steel plates thicker than 50 mm and up to and including 200 mm in thickness,Pratiques recommandées pour l'examen radiographique de joints soudés par fusion — Partie 2: Joints soudés bout à bout par fusion de tôles d'acier d'épaisseur supérieure à 50 mm mais inférieure ou égale à 200 mm,1985-05-23,1,['25.160.40'],ISO/TC 44/SC 5,9599,[7302],[29970],"['en','fr']",5,"<p>Specifies general techniques of weld radiography with the object of enabling satisfactory results to be obtained economically. The techniques are based on generally accepted practice and the fu

5626,IS,,ISO 1106-3:1984,Recommended practice for radiographic examination of fusion welded joints — Part 3: Fusion welded circumferential joints in steel pipes of up to 50 mm wall thickness,Pratique recommandée pour l'examen radiographique de joints soudés par fusion — Partie 3: Joints circulaires soudés par fusion de tubes d'acier d'épaisseur inférieure ou égale à 50 mm,1984-12-01,1,['25.160.40'],ISO/TC 44/SC 5,9599,"[5367,5368]",[29970],"['en','fr']",14,<p>The detection of flaws in an item submitted to X- or gamma-radio-graphic examination depends on the particularities of the technique employed. This part of ISO 1106 specifies general techniques of weld radiography with the object of ena

50025,IS,,ISO 11063:2012,Soil quality — Method to directly extract DNA from soil samples,Qualité du sol — Méthode pour extraire directement l'ADN d'échantillons de sol,2012-02-06,1,['13.080.30'],ISO/TC 190/SC 4,9599,,[75810],"['en','fr']",23,"<p>This International Standard specifies a method for direct extraction of DNA from soil samples to analyse the</p><p>global structure and the abundance of soil bacterial communities using PCR-based technologies. This method</p><p>is mainly dedicated to agricultural and forest soils. This method can possibly not be suitable for soils rich in</p><p>organic matter (e.g. peat soils) or soils heavily polluted with organic pollutants or heavy metals.</p><p>T

19045,IS,,ISO 11064-4:2004,Ergonomic design of control centres — Part 4: Layout and dimensions of workstations,Conception ergonomique des centres de commande — Partie 4: Agencement et dimensionnement du poste de travail,2004-07-01,1,['13.180'],ISO/TC 159/SC 4,9599,,[54419],"['en','fr']",30,"<p>ISO 11064-4:2004 specifies ergonomic principles, recommendations and requirements for the design of workstations found in control centres. It covers workstation design with particular emphasis on layout and dimensions. This standard covers primarily seated, visual-display-based workstations although sit/stand workstations are also addressed. These workstations are to be found in applications such as tr

5627,IS,,ISO 1107:1974,Fishing nets — Netting — Basic terms and definitions,Filets de pêche — Nappes de filet — Termes fondamentaux et définitions,1974-02-01,1,"['01.040.65','65.150']",ISO/TC 38,9599,,[34628],"['en','fr']",3,"<p>Provides examples (with figure) for the determination of length of mesh side, length of mesh, opening of mesh, direction in knotted netting, direction in knotless netting, and size of netting. - Replaces ISO Recommendation R 1107-1969.</p>"

34628,IS,,ISO 1107:2003,Fishing nets — Netting — Basic terms and definitions,Filets de pêche — Nappes de filet — Termes fondamentaux et définitions,2003-06-16,2,"['01.040.65','65.150']",ISO/TC 38,9599,[5627],[72227],"['en','fr']",7,"<p>ISO 1107:2003 gives the principal terms relating to netting for fishing nets, together with their definitions or, in some cases, the method of expressing dimensions.</p>"

19052,IS,,ISO 11070:1998,"Sterile, single-use intravascular catheter introducers","Introducteurs de cathéters intravasculaires stériles, non réutilisables",1998-04-30,1,['11.040.25'],ISO/TC 84,9599,,[63315],"['en','fr']",23,

46493,IS,,ISO 11073-91064:2009,Health informatics — Standard communication protocol — Part 91064: Computer-assisted electrocardiography,Informatique de santé — Communication entre dispositifs médicaux sur le site des soins — Partie 91064: Protocole de communication standard pour l'électrocardiographie assistée par ordinateur,2009-05-05,1,['35.240.80'],ISO/TC 215,9599,,[84664],['en'],159,"<p>ISO 11073-91064:2009 specifies the common conventions required for the cart-to-host as well as cart-to-cart interchange of specific patient data (demographic, recording, ...), ECG signal data, ECG measurement and ECG interpretation results.</p><p>ISO 11073-91064:2009 specifies the content and structure o

19061,IS,,ISO 11074-1:1996,Soil quality — Vocabulary — Part 1: Terms and definitions relating to the protection and pollution of the soil,Qualité du sol — Vocabulaire — Partie 1: Termes et définitions relatifs à la protection et à la pollution du sol,1996-08-01,1,"['01.040.13','13.080.01']",ISO/TC 190,9599,,"[37840,38529,20634]","['en','fr','ru']",22,"<p>Defines terms used in certain fields of soil quality characterization. Covers terms relating to soil protection, soil pollution and soil damage.</p>"

19062,IS,,ISO 11074-2:1998,Soil quality — Vocabulary — Part 2: Terms and definitions relating to sampling,Qualité du sol — Vocabulaire — Partie 2: Termes et définitions relatifs à l'échantillonnage,1998-11-19,1,"['01.040.13','13.080.01']",ISO/TC 190,9599,,"[37841,38529]","['en','fr']",23,