| Name |
Description |
Abstract |
Status |
Publication date |
Edition |
Number of pages |
Technical committee |
ICS |
| ISO/TS 27687:2008 |
Nanotechnologies — Terminology and definitions for nano-objects — Nanoparticle, nanofibre and nanoplate |
ISO/TS 27687:2008 lists unambiguous terms and definitions related to particles in the field of nanotechnologies. It is intended to facilitate communications between organizations and individuals in industry and those who interact with them.
|
Withdrawn |
2008-08 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO 15561:1998 |
Practice for use of a dichromate dosimetry system |
|
Withdrawn |
1998-12 |
Edition : 1 |
Number of pages : 6 |
Technical Committee |
17.240
Radiation measurements
|
| ISO 29701:2010 |
Nanotechnologies — Endotoxin test on nanomaterial samples for in vitro systems — Limulus amebocyte lysate (LAL) test |
ISO 29701:2010 describes the application of a test using Limulus amebocyte lysate (LAL) reagent for the evaluation of nanomaterials intended for cell-based in vitro biological test systems. The test is suitable for use with nanomaterial samples dispersed in aqueous media, e.g. water, serum or reaction medium, and to such media incubated with nanomaterials for an appropriate duration at 37 °C.
ISO 29701:2010 is restricted to test samples for in vitro systems, but the methods can also be adapted to nanomaterials to be administered to animals by parenteral routes.
|
Published |
2010-09 |
Edition : 1 |
Number of pages : 20 |
Technical Committee |
07.120
Nanotechnologies
;
11.100.10
In vitro diagnostic test systems
|
| IEC/CD 62565-3-1 |
Nanomanufacturing — Material specifications — Part 3-1: Graphene — Blank detail specification |
|
Under development |
|
Edition : 1 |
|
Technical Committee |
07.120
Nanotechnologies
|
| IEC/TS 62607-2-1:2012 |
Nanomanufacturing - key control characteristics for CNT film applications - Resistivity — Part 2-1: |
This part of IEC 62607 provides a standardized method for categorizing a grade of
commercial CNTs in terms of their electrical properties to enable a user to select a CNT
material suitable for their application. The method is intended to assess whether the delivered
materials from different production batches of the same production process are comparable
regarding electrical properties of the final product which are related to electrical conductivity.
The correlation between the measured parameters by the proposed method and a relevant
product performance parameter has to be established for every application. This specification
includes
a) definitions of terminology used in this document,
b) recommendations for sample preparation,
c) outlines of the experimental procedures to measure sheet resistance of CNTs in thin films,
d) methods of interpretation of results and discussion of data analysis,
e) case studies and,
f) references.
|
Published |
2012-05 |
Edition : 1 |
Number of pages : 11 |
Technical Committee |
07.120
Nanotechnologies
|
| IEC/TS 62622:2012 |
Artificial gratings used in nanotechnology — Description and measurement of dimensional quality parameters |
IEC/TS 62622:2012(E), which is a technical specification, specifies the generic terminology for the global and local quality parameters of artificial gratings, interpreted in terms of deviations from nominal positions of grating features, and provides guidance on the categorization of measurement and evaluation methods for their determination. This specification is intended to facilitate communication among manufacturers, users and calibration laboratories dealing with the characterization of the dimensional quality parameters of artificial gratings used in nanotechnology. This specification supports quality assurance in the production and use of artificial gratings in different areas of application in nanotechnology. Whilst the definitions and described methods are universal to a large variety of different gratings, the focus is on one-dimensional (1D) and two-dimensional (2D) gratings.
|
Published |
2012-10 |
Edition : 1 |
Number of pages : 34 |
Technical Committee |
07.120
Nanotechnologies
|
| IEC/TR 63258:2021 |
Nanotechnologies — A guideline for ellipsometry application to evaluate the thickness of nanoscale films |
IEC TR 63258:2021 is a Technical Report focused on the practical protocol of ellipsometry to evaluate the thickness of nanoscale films. This document does not include any specification of the ellipsometers, but suggests how to minimize the data variation to improve data reproducibility.
|
Published |
2021-03 |
Edition : 1 |
Number of pages : 16 |
Technical Committee |
07.120
Nanotechnologies
|
| ISO/FDIS 80004-1 |
Nanotechnologies – Vocabulary — Part 1: Core vocabulary |
|
Under development |
|
Edition : 1 |
Number of pages : 12 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-1:2010 |
Nanotechnologies — Vocabulary — Part 1: Core terms |
ISO/TS 80004-1:2010 lists terms and definitions related to core terms in the field of nanotechnologies. It is intended to facilitate communications between organizations and individuals in industry and those who interact with them.
|
Withdrawn |
2010-10 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-1:2015 |
Nanotechnologies — Vocabulary — Part 1: Core terms |
ISO/TS 80004-1:2015 lists terms and definitions related to core terms in the field of nanotechnologies. It is intended to facilitate communications between organizations and individuals in industry and those who interact with them.
|
Published |
2015-12 |
Edition : 2 |
Number of pages : 3 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-2:2015 |
Nanotechnologies — Vocabulary — Part 2: Nano-objects |
ISO/TS 80004-2:2015 lists terms and definitions related to particles in the field of nanotechnologies.
|
Published |
2015-06 |
Edition : 1 |
Number of pages : 10 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO 3310-1:1990 |
Test sieves — Technical requirements and testing — Part 1: Test sieves of metal wire cloth |
|
Withdrawn |
1990-06 |
Edition : 3 |
Number of pages : 7 |
Technical Committee |
19.120
Particle size analysis. Sieving
|
| ISO/TS 80004-3:2010 |
Nanotechnologies — Vocabulary — Part 3: Carbon nano-objects |
ISO/TS 80004-3:2010 lists terms and definitions related to carbon nano-objects in the field of nanotechnologies. It is intended to facilitate communications between organizations and individuals in industry and those who interact with them.
|
Withdrawn |
2010-05 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-3:2020 |
Nanotechnologies — Vocabulary — Part 3: Carbon nano-objects |
This document defines terms related to carbon nano-objects in the field of nanotechnologies.
It is intended to facilitate communication between organizations' and individuals' research, industry and other interested parties and those who interact with them. Additional terms and definitions for graphene and two-dimensional materials (2D) materials are provided in ISO/TS 80004-13.
Related carbon nanoscale materials are given in Annex A.
|
Published |
2020-11 |
Edition : 2 |
Number of pages : 11 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-4:2011 |
Nanotechnologies — Vocabulary — Part 4: Nanostructured materials |
ISO/TS 80004-4:2011 gives terms and definitions for materials in the field of nanotechnologies where one or more components are nanoscale regions and the materials exhibit properties attributable to the presence of those nanoscale regions. It is intended to facilitate communications between organizations and individuals in industry and those who interact with them.
Materials classified as nanostructured have an internal or surface structure with a significant fraction of features, grains, voids or precipitates in the nanoscale. Articles that contain nano-objects or nanostructured materials are not necessarily nanostructured materials themselves.
ISO/TS 80004-4:2011 includes nanodispersion.
|
Published |
2011-12 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-5:2011 |
Nanotechnologies — Vocabulary — Part 5: Nano/bio interface |
ISO/TS 80004-5:2011 lists terms and definitions related to the interface between nanomaterials and biology. It is intended to facilitate communications between scientists, engineers, technologists, designers, manufacturers, regulators, NGOs, consumer organizations, members of the public and others with an interest in:
the application or use of nanotechnologies in biology or biotechnology;
the use of biological matter or principles in nanotechnology.
|
Published |
2011-12 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-6:2013 |
Nanotechnologies — Vocabulary — Part 6: Nano-object characterization |
ISO/TS 80004-6:2013 lists terms and definitions relevant to the characterization of nano-objects.
|
Withdrawn |
2013-11 |
Edition : 1 |
Number of pages : 24 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-6:2021 |
Nanotechnologies — Vocabulary — Part 6: Nano-object characterization |
This document defines terms related to the characterization of nano-objects in the field of nanotechnologies.
It is intended to facilitate communication between organizations and individuals in research, industry and other interested parties and those who interact with them.
|
Published |
2021-03 |
Edition : 2 |
Number of pages : 24 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-7:2011 |
Nanotechnologies — Vocabulary — Part 7: Diagnostics and therapeutics for healthcare |
ISO/TS 80004-7:2011 is applicable to the use of nanotechnologies in medical diagnostics and therapeutics. Terms relating to the applications of nanotechnology in healthcare might also be addressed in other parts of ISO/TS 80004 and in other documents.
Terms relating to the exploitation of material features at the nanoscale for diagnostic or therapeutic purposes in relation to human disease come within the scope of ISO/TS 80004-7:2011. Nanoscale properties can be embodied in materials that contain nanoscale elements, or are themselves of nanoscale dimensions.
ISO/TS 80004-7:2011 provides consistent and unambiguous use of terms for healthcare professionals, manufacturers, consumers, technologists, patent agents, regulators, NGOs, and researchers, etc.
|
Published |
2011-10 |
Edition : 1 |
Number of pages : 8 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-8:2013 |
Nanotechnologies — Vocabulary — Part 8: Nanomanufacturing processes |
ISO/TS 80004-8:2013 gives terms and definitions related to nanomanufacturing processes in the field of nanotechnologies. It forms one part of multi-part terminology and definitions documentation covering the different aspects of nanotechnologies.
|
Withdrawn |
2013-12 |
Edition : 1 |
Number of pages : 27 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO 454:1975 |
Acoustics — Relation between sound pressure levels of narrow bands of noise in a diffuse field and in a frontally-incident free field for equal loudness |
|
Withdrawn |
1975-01 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
13.140
Noise with respect to human beings
|
| ISO/TS 80004-8:2020 |
Nanotechnologies — Vocabulary — Part 8: Nanomanufacturing processes |
This document defines terms related to nanomanufacturing processes in the field of nanotechnologies.
All the process terms in this document are relevant to nanomanufacturing, however, many of the listed processes are not exclusively relevant to the nanoscale. Terms that are not exclusive are noted within the definitions. Depending on controllable conditions, such processes can result in material features at the nanoscale or, alternatively, at larger scales.
There are many other terms that name tools, components, materials, systems control methods or metrology methods associated with nanomanufacturing that are beyond the scope of this document.
Terms and definitions from other parts of the ISO/TS 80004 series are reproduced in Clause 3 for context and better understanding.
|
Published |
2020-11 |
Edition : 2 |
Number of pages : 29 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| IEC/TS 80004-9:2017 |
Nanotechnologies — Vocabulary — Part 9: Nano-enabled electrotechnical products and systems |
IEC TS 80004-9: 2017(E) specifies terms and definitions for electrotechnical products and systems reliant on nanomaterials for their essential functionalities. It is intended to facilitate communications between organizations and individuals in industry and those who interact with them.
|
Published |
2017-01 |
Edition : 1 |
Number of pages : 6 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-11:2017 |
Nanotechnologies — Vocabulary — Part 11: Nanolayer, nanocoating, nanofilm, and related terms |
ISO/TS 80004-11:2017 lists terms and definitions, and specifies an extensible taxonomic terminology framework for nanolayers, nanocoatings, nanofilms, and related terms in the field of nanotechnologies.
|
Published |
2017-05 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-12:2016 |
Nanotechnologies — Vocabulary — Part 12: Quantum phenomena in nanotechnology |
ISO/TS 80004-12:2016 lists terms and definitions relevant to quantum phenomena in nanotechnologies.
All of these terms are important for nanotechnologies, but it is to be noted that many of them are not exclusively relevant to the nanoscale and can also be used to some extent to refer to larger scales.
The list of terms presented does not claim to provide exhaustive coverage of the whole spectrum of quantum concepts and phenomena in nanotechnology. It covers important phenomena as acknowledged by many stakeholders from academia, industry, etc.
ISO/TS 80004-12:2016 is intended to facilitate communication between organizations and individuals in industry and those who interact with them.
|
Published |
2016-04 |
Edition : 1 |
Number of pages : 12 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/TS 80004-13:2017 |
Nanotechnologies — Vocabulary — Part 13: Graphene and related two-dimensional (2D) materials |
ISO/TS 80004-13:2017 lists terms and definitions for graphene and related two-dimensional (2D) materials, and includes related terms naming production methods, properties and their characterization.
It is intended to facilitate communication between organizations and individuals in research, industry and other interested parties and those who interact with them.
|
Published |
2017-09 |
Edition : 1 |
Number of pages : 21 |
Technical Committee |
07.120
Nanotechnologies
;
01.040.07
Natural and applied sciences (Vocabularies)
|
| ISO/CD TS 80004-13 |
Nanotechnologies — Vocabulary — Part 13: Graphene and other two-dimensional (2D) materials |
ISO/TS 80004-13:2017 lists terms and definitions for graphene and related two-dimensional (2D) materials, and includes related terms naming production methods, properties and their characterization.
It is intended to facilitate communication between organizations and individuals in research, industry and other interested parties and those who interact with them.
|
Under development |
|
Edition : 2 |
|
Technical Committee |
07.120
Nanotechnologies
|
| ISO 18385:2016 |
Minimizing the risk of human DNA contamination in products used to collect, store and analyze biological material for forensic purposes — Requirements |
ISO 18385:2016 specifies requirements for the production of products used in the collection, storage, and analysis of biological material for forensic DNA purposes, but not those consumables and reagents used in post-amplification analysis.
The consumables and reagents covered by this International Standard include those used for evidence collection (sampling kits), such as swabs, containers, and packaging, and also products used in the analysis of DNA samples, such as tubes and other plasticware, disposable laboratory coats, gloves, and other consumables.
ISO 18385:2016 applies to the production of consumables and reagents which do not require cleaning for continued use. This International Standard does not cover technical product specifications (i.e. product design).
ISO 18385:2016 excludes microbiological testing.
ISO 18385:2016 specifies a requirement for manufacturers to minimize the risk of occurrence of detectable human nuclear DNA contamination in products used by the global forensic community.
|
Published |
2016-02 |
Edition : 1 |
Number of pages : 19 |
Technical Committee |
07.140
Forensic science
|
| ISO 21043-1:2018 |
Forensic sciences — Part 1: Terms and definitions |
This document defines terms used in the ISO 21043 series of standards.
|
Published |
2018-08 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
07.140
Forensic science
|
| ISO 21043-2:2018 |
Forensic sciences — Part 2: Recognition, recording, collecting, transport and storage of items |
This document specifies requirements for the forensic process focusing on recognition, recording, collection, transport and storage of items of potential forensic value. It includes requirements for the assessment and examination of scenes but is also applicable to activities that occur within the facility. This document also includes quality requirements.
This document is not applicable to procedures for the recovery of data from digital storage media which is covered by ISO/IEC 27037. However, the storage medium itself can yield additional items of forensic value (e.g. fingerprints or DNA).
Annex D shows the applicability of this document to the forensic process.
|
Published |
2018-08 |
Edition : 1 |
Number of pages : 13 |
Technical Committee |
07.140
Forensic science
|
| ISO/CD 21043-3.2 |
Forensic Sciences — Part 3: Analysis |
The purpose of this Standard is to set out standard practices for analysis of material for forensic purposes.
The committee is working on a series which, when complete, will include—
Part 1: Terms and definitions
Part 2: Recognition, recording, collection and storage of material
Part 3: Analysis (this Standard)
Part 4: Interpretation
Part 5: Reporting
Part 1 and 2 have been published
|
Under development |
|
Edition : 1 |
|
Technical Committee |
07.140
Forensic science
|
| ISO/CD 21043-4.2 |
Forensic Sciences — Part 4: Interpretation |
The purpose of this Standard is to set out standard practices for interpreting forensic results.
The committee is working on a series which, when complete, will include—
Part 1: Terms and definitions
Part 2: Recognition, recording, collection and storage of material
Part 3: Analysis
Part 4: Interpretation (this Standard)
Part 5: Reporting
Part 1 and 2 have been published
|
Under development |
|
Edition : 1 |
|
Technical Committee |
07.140
Forensic science
|
| ISO/CD 21043-5.2 |
Forensic Sciences — Part 5: Reporting |
The purpose of this Standard is to set out standard practices for reporting forensic results.
The committee is working on a series which, when complete, will include—
Part 1: Terms and definitions
Part 2: Recognition, recording, collection and storage of material
Part 3: Analysis
Part 4: Interpretation
Part 5: Reporting (this standard)
Part 1 and 2 are published.
|
Under development |
|
Edition : 1 |
|
Technical Committee |
07.140
Forensic science
|
| IWA 1:2001 |
Quality management systems — Guidelines for process improvements in health service organizations |
|
Withdrawn |
2001-10 |
Edition : 1 |
Number of pages : 68 |
Technical Committee |
11.020
Medical sciences and health care facilities in general
;
03.120.10
Quality management and quality assurance
|
| IWA 1:2005 |
Quality management systems — Guidelines for process improvements in health service organizations |
IWA 1:2005 provides additional guidance for any health service organization involved in the management, delivery, or administration of health service products or services, including training and/or research, in the life continuum process for human beings, regardless of type, size and the product or service provided.
|
Withdrawn |
2005-10 |
Edition : 2 |
Number of pages : 84 |
Technical Committee |
11.020
Medical sciences and health care facilities in general
;
03.120.10
Quality management and quality assurance
|
| ISO/IEC Guide 63:1999 |
Guide to the development and inclusion of safety aspects in International Standards for medical devices |
|
Withdrawn |
1999-02 |
Edition : 1 |
Number of pages : 8 |
Technical Committee |
01.120
Standardization. General rules
;
11.020
Medical sciences and health care facilities in general
|
| ISO/ASTM 51939:2002 |
Practice for blood irradiation dosimetry |
ISO/ASTM 51939 outlines irradiator installation qualification and dosimetric procedures to be followed in the irradiation of blood and blood products by the blood-banking community. If followed, these procedures will help to ensure that the products processed with ionizing radiation from gamma, bremsstrahlung X-rays or electron sources receive absorbed doses within a predetermined range.
ISO/ASTM 51939 covers dosimetry for the irradiation of blood for the following types of irradiators: self-contained dry-storage 137Cs or 60Co irradiators (free-standing irradiators), tele-therapy units, self-contained bremsstrahlung X-ray units and electron accelerators. The absorbed dose range for blood irradiation is typically 15 Gy to 50 Gy.
This International Standard also covers the use of radiation-sensitive indicators for the visual and qualitative indication that the product has been irradiated. It is intended for use by technically and non-technically oriented people and, therefore, contains more tutorial information than many other ISO/ASTM dosimetry standards.
|
Withdrawn |
2002-03 |
Edition : 1 |
Number of pages : 12 |
Technical Committee |
11.020
Medical sciences and health care facilities in general
;
17.240
Radiation measurements
|
| ISO 10993-3:1992 |
Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity |
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.
|
Withdrawn |
1992-12 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
11.100
Laboratory medicine
|
| ISO 726:1982 |
Metallic materials — Hardness test — Calibration of standardized blocks to be used for Brinell hardness testing machines |
|
Withdrawn |
1982-06 |
Edition : 1 |
Number of pages : 3 |
Technical Committee |
77.040.10
Mechanical testing of metals
|
| ISO/ASTM 51939:2005 |
Practice for blood irradiation dosimetry |
ISO/ASTM 51939:2005 outlines irradiator installation qualification, operational qualification, performance qualification, and routine product processing dosimetric procedures to be followed in the irradiation of blood and blood components by the blood-banking community. If followed, these procedures will help to ensure that the products processed with ionizing radiation from gamma, X-rays (bremsstrahlung), or electron sources receive absorbed doses within a predetermined range.
ISO/ASTM 51939:2005 also covers the use of radiation-sensitive indicators for the visual and qualitative indication that the product has been irradiated.
|
Withdrawn |
2005-05 |
Edition : 2 |
Number of pages : 13 |
Technical Committee |
11.020
Medical sciences and health care facilities in general
;
17.240
Radiation measurements
|
| ISO 18385:2016 |
Minimizing the risk of human DNA contamination in products used to collect, store and analyze biological material for forensic purposes — Requirements |
ISO 18385:2016 specifies requirements for the production of products used in the collection, storage, and analysis of biological material for forensic DNA purposes, but not those consumables and reagents used in post-amplification analysis.
The consumables and reagents covered by this International Standard include those used for evidence collection (sampling kits), such as swabs, containers, and packaging, and also products used in the analysis of DNA samples, such as tubes and other plasticware, disposable laboratory coats, gloves, and other consumables.
ISO 18385:2016 applies to the production of consumables and reagents which do not require cleaning for continued use. This International Standard does not cover technical product specifications (i.e. product design).
ISO 18385:2016 excludes microbiological testing.
ISO 18385:2016 specifies a requirement for manufacturers to minimize the risk of occurrence of detectable human nuclear DNA contamination in products used by the global forensic community.
|
Published |
2016-02 |
Edition : 1 |
Number of pages : 19 |
Technical Committee |
07.140
Forensic science
|
| ISO 21043-1:2018 |
Forensic sciences — Part 1: Terms and definitions |
This document defines terms used in the ISO 21043 series of standards.
|
Published |
2018-08 |
Edition : 1 |
Number of pages : 5 |
Technical Committee |
07.140
Forensic science
|
| ISO 21043-2:2018 |
Forensic sciences — Part 2: Recognition, recording, collecting, transport and storage of items |
This document specifies requirements for the forensic process focusing on recognition, recording, collection, transport and storage of items of potential forensic value. It includes requirements for the assessment and examination of scenes but is also applicable to activities that occur within the facility. This document also includes quality requirements.
This document is not applicable to procedures for the recovery of data from digital storage media which is covered by ISO/IEC 27037. However, the storage medium itself can yield additional items of forensic value (e.g. fingerprints or DNA).
Annex D shows the applicability of this document to the forensic process.
|
Published |
2018-08 |
Edition : 1 |
Number of pages : 13 |
Technical Committee |
07.140
Forensic science
|
| ISO/CD 21043-3.2 |
Forensic Sciences — Part 3: Analysis |
The purpose of this Standard is to set out standard practices for analysis of material for forensic purposes.
The committee is working on a series which, when complete, will include—
Part 1: Terms and definitions
Part 2: Recognition, recording, collection and storage of material
Part 3: Analysis (this Standard)
Part 4: Interpretation
Part 5: Reporting
Part 1 and 2 have been published
|
Under development |
|
Edition : 1 |
|
Technical Committee |
07.140
Forensic science
|
| ISO/CD 21043-4.2 |
Forensic Sciences — Part 4: Interpretation |
The purpose of this Standard is to set out standard practices for interpreting forensic results.
The committee is working on a series which, when complete, will include—
Part 1: Terms and definitions
Part 2: Recognition, recording, collection and storage of material
Part 3: Analysis
Part 4: Interpretation (this Standard)
Part 5: Reporting
Part 1 and 2 have been published
|
Under development |
|
Edition : 1 |
|
Technical Committee |
07.140
Forensic science
|
| ISO/CD 21043-5.2 |
Forensic Sciences — Part 5: Reporting |
The purpose of this Standard is to set out standard practices for reporting forensic results.
The committee is working on a series which, when complete, will include—
Part 1: Terms and definitions
Part 2: Recognition, recording, collection and storage of material
Part 3: Analysis
Part 4: Interpretation
Part 5: Reporting (this standard)
Part 1 and 2 are published.
|
Under development |
|
Edition : 1 |
|
Technical Committee |
07.140
Forensic science
|
| ISO/TR 7405:1984 |
Biological evaluation of dental materials |
|
Withdrawn |
1984-01 |
Edition : 1 |
Number of pages : 54 |
Technical Committee |
11.100
Laboratory medicine
;
11.060.10
Dental materials
|
| ISO 10993-1:1992 |
Biological evaluation of medical devices — Part 1: Guidance on selection of tests |
|
Withdrawn |
1992-04 |
Edition : 1 |
Number of pages : 11 |
Technical Committee |
11.100
Laboratory medicine
|
| ISO 10993-1:1992/Cor 1:1992 |
Biological evaluation of medical devices — Part 1: Guidance on selection of tests — Technical Corrigendum 1 |
|
Withdrawn |
1992-09 |
Edition : 1 |
Number of pages : 1 |
Technical Committee |
11.100
Laboratory medicine
|
| ISO 10993-4:1992 |
Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood |
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 during in vivo function.
|
Withdrawn |
1992-12 |
Edition : 1 |
Number of pages : 19 |
Technical Committee |
11.100
Laboratory medicine
|
| ISO 10993-5:1992 |
Biological evaluation of medical devices — Part 5: Tests for cytotoxicity: in vitro methods |
|
Withdrawn |
1992-12 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
11.100
Laboratory medicine
|
| ISO/TR 10993-9:1994 |
Biological evaluation of medical devices — Part 9: Degradation of materials related to biological testing |
|
Withdrawn |
1994-07 |
Edition : 1 |
Number of pages : 34 |
Technical Committee |
11.100
Laboratory medicine
|
| ISO 10993-10:1995 |
Biological evaluation of medical devices — Part 10: Tests for irritation and sensitization |
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.
|
Withdrawn |
1995-03 |
Edition : 1 |
Number of pages : 31 |
Technical Committee |
11.100
Laboratory medicine
|
| ISO 10993-12:1996 |
Biological evaluation of medical devices — Part 12: Sample preparation and reference materials |
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.
|
Withdrawn |
1996-09 |
Edition : 1 |
Number of pages : 11 |
Technical Committee |
11.100
Laboratory medicine
|
| ISO 14155:1996 |
Clinical investigation of medical devices |
Pertains to the clinical investigation in human subjects of those medical devices whose clinical performance needs assessment. Specifies the requirements for conducting the clinical investigation and documentation. Provides the framework for systematic written procedures for the organization, design, implementation and data collection.
|
Withdrawn |
1996-02 |
Edition : 1 |
Number of pages : 12 |
Technical Committee |
11.100
Laboratory medicine
|
| ISO 10282:1994 |
Single-use sterile surgical rubber gloves — Specification |
Specifies requirements for packaged sterile gloves intended for use in surgical procedures to protect the patient and the user from cross-contamination. Applicable to single-use gloves that are worn once and then discarded. Does not apply to examination or procedure gloves. Intended as a reference for the performance and safety of rubber surgical gloves.
|
Withdrawn |
1994-11 |
Edition : 1 |
Number of pages : 8 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 10282:2002 |
Single-use sterile rubber surgical gloves — Specification |
ISO 10282:2002 specifies requirements for packaged sterile rubber gloves intended for use in surgical procedures to protect the patient and the user from cross-contamination. It is applicable to single-use gloves that are worn once and then discarded. It does not apply to examination or procedure gloves. It covers gloves with smooth surfaces and gloves with textured surfaces over part or all of the glove.
This standard is intended as a reference for the performance and safety of rubber surgical gloves. The safe and proper usage of surgical gloves and sterilization procedures with subsequent handling, packaging and storage procedures are outside the scope of this International Standard.
|
Withdrawn |
2002-09 |
Edition : 2 |
Number of pages : 10 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 10282:2002/Cor 1:2005 |
Single-use sterile rubber surgical gloves — Specification — Technical Corrigendum 1 |
|
Withdrawn |
2005-06 |
Edition : 2 |
Number of pages : 1 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 10282:2014 |
Single-use sterile rubber surgical gloves — Specification |
ISO 10282:2014 specifies requirements for packaged sterile rubber gloves intended for use in surgical procedures to protect the patient and the user from cross-contamination. It is applicable to single-use gloves that are worn once and then discarded. It does not apply to examination or procedure gloves. It covers gloves with smooth surfaces and gloves with textured surfaces over part or the whole glove.
ISO 10282:2014 is intended as a reference for the performance and safety of rubber surgical gloves. The safe and proper usage of surgical gloves and sterilization procedures with subsequent handling, packaging, and storage procedures are outside the scope of ISO 10282:2014.
|
Withdrawn |
2014-02 |
Edition : 3 |
Number of pages : 11 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 7930:1986 |
Wheelchairs — Type classification based on appearance characteristics |
|
Withdrawn |
1986-05 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
11.180
Aids for disabled or handicapped persons
|
| ISO 10282:2023 |
Single-use sterile rubber surgical gloves — Specification |
This document specifies requirements for packaged sterile rubber gloves intended for use in surgical procedures to protect the patient and the user from cross-contamination.
This document is applicable to single-use gloves that are worn once and then discarded. It does not apply to examination or procedure gloves.
This document covers gloves with smooth surfaces and gloves with textured surfaces over part or the whole glove.
This document is intended to be a reference for the performance and safety of rubber surgical gloves. The safe and proper usage of surgical gloves and sterilization procedures with subsequent handling, packaging and storage procedures are outside the scope of this document.
|
Published |
2023-02 |
Edition : 4 |
Number of pages : 11 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 11193-1:2002 |
Single-use medical examination gloves — Part 1: Specification for gloves made from rubber latex or rubber solution |
ISO 11193-1 specifies requirements for packaged sterile, or bulked non-sterile, rubber gloves intended for use in medical examinations and diagnostic or therapeutic procedures to protect the patient and the user from cross-contamination. It also covers rubber gloves intended for use in handling contaminated medical materials and gloves with smooth surfaces or with textured surfaces over part or all of the glove.
This standard is intended as a reference for the performance and safety of rubber examination gloves. The safe and proper usage of examination gloves and sterilization procedures with subsequent handling, packaging and storage procedures are outside the scope of this standard.
|
Withdrawn |
2002-11 |
Edition : 1 |
Number of pages : 9 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 11193-1:2002/Amd 1:2007 |
Single-use medical examination gloves — Part 1: Specification for gloves made from rubber latex or rubber solution — Amendment 1 |
|
Withdrawn |
2007-05 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 11193-1:2002/Cor 1:2005 |
Single-use medical examination gloves — Part 1: Specification for gloves made from rubber latex or rubber solution — Technical Corrigendum 1 |
|
Withdrawn |
2005-06 |
Edition : 1 |
Number of pages : 1 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 11193-1:2008 |
Single-use medical examination gloves — Part 1: Specification for gloves made from rubber latex or rubber solution |
ISO 11193-1:2008 specifies requirements for packaged sterile, or bulked non-sterile, rubber gloves intended for use in medical examinations and diagnostic or therapeutic procedures to protect the patient and the user from cross-contamination. It also covers rubber gloves intended for use in handling contaminated medical materials and gloves with smooth surfaces or with textured surfaces over all or part of the glove.
This part of ISO 11193 is intended as a reference for the performance and safety of rubber examination gloves. It does not cover the safe and proper usage of examination gloves and sterilization procedures with subsequent handling, packaging and storage procedures.
|
Withdrawn |
2008-09 |
Edition : 2 |
Number of pages : 9 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 11193-1:2008/Amd 1:2012 |
Single-use medical examination gloves — Part 1: Specification for gloves made from rubber latex or rubber solution — Amendment 1 |
|
Withdrawn |
2012-06 |
Edition : 2 |
Number of pages : 1 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 11193-1:2020 |
Single-use medical examination gloves — Part 1: Specification for gloves made from rubber latex or rubber solution |
This document specifies requirements for packaged sterile, or bulked non-sterile, rubber gloves intended for use in medical examinations and diagnostic or therapeutic procedures to protect the patient and the user from cross-contamination. It also covers rubber gloves intended for use in handling contaminated medical materials and gloves with smooth surfaces or with textured surfaces over all or part of the glove.
This document is intended as a reference for the performance and safety of rubber examination gloves. It does not cover the safe and proper usage of examination gloves and sterilization procedures with subsequent handling, packaging and storage procedures.
|
Published |
2020-08 |
Edition : 3 |
Number of pages : 10 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 11193-2:2006 |
Single-use medical examination gloves — Part 2: Specification for gloves made from poly(vinyl chloride) |
ISO 11193-2:2006 specifies requirements for packaged sterile, or bulked non-sterile, poly(vinyl chloride) gloves intended for use in medical examinations, and diagnostic or therapeutic procedures, to protect the patient and the user from cross-contamination. It also covers poly(vinyl chloride) gloves intended for use in handling contaminated medical materials.
ISO 11193-2:2006 is intended as a reference for the performance and safety of poly(vinyl chloride) examination gloves. The safe and proper usage of examination gloves and sterilization procedures with subsequent handling, packaging and storage procedures are outside the scope of ISO 11193-2:2006.
|
Published |
2006-11 |
Edition : 1 |
Number of pages : 10 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 11193:1994 |
Single-use rubber examination gloves — Specification |
Specifies requirements for packaged sterile, or bulked non-sterile, rubber gloves intended for use in medical examinations and diagnostic or therapeutic procedures to protect the patient and the user from cross-contamination. Also covers rubber gloves intended for use in handling contaminated medical materials. Applies to single-use gloves, gloves with smooth surfaces or with textured surfaces over part or all of the glove. Does not apply to gloves made from plastic film either of a dipped or welded construction or as a substitute for gloves for use in surgical procedures. Intended as a reference for the performance and safety of rubber examination gloves.
|
Withdrawn |
1994-11 |
Edition : 1 |
Number of pages : 7 |
Technical Committee |
11.140
Hospital equipment
;
83.140.99
Other rubber and plastics products
|
| ISO 21171:2006 |
Medical gloves — Determination of removable surface powder |
ISO 21171:2006 specifies methods for the determination of readily removable powder on the surface of gloves for medical use. Three methods are specified: method A for powdered gloves and methods B and C for powder-free gloves. This International Standard does not address safety issues that may be associated with the presence of powder on gloves nor does it prescribe limits on the amounts that may be present. The applicability of this International Standard to medical gloves not made from rubber has not been established.
|
Published |
2006-05 |
Edition : 1 |
Number of pages : 9 |
Technical Committee |
11.140
Hospital equipment
|
| ISO 22609:2004 |
Clothing for protection against infectious agents — Medical face masks — Test method for resistance against penetration by synthetic blood (fixed volume, horizontally projected) |
ISO 22609:2004 describes a laboratory test method for measuring the
resistance of medical face masks to penetration by a splash of synthetic
blood.
ISO 22609:2004 primarily addresses the performance of materials or certain
material constructions used in medical face masks. The test method does not
address the performance of the medical face mask's design, construction,
interfaces or other factors which may affect the overall protection offered by
the medical face mask and its operation (such as filtration efficiency and
pressure drop).
ISO 22609:2004 does not evaluate the performance of medical face masks as a
protection against contamination via airborne exposure pathways or in the
prevention of the penetration of aerosolized body fluids deposited on the
medical face mask.
|
Published |
2004-12 |
Edition : 1 |
Number of pages : 17 |
Technical Committee |
11.140
Hospital equipment
;
13.340.10
Protective clothing
|
| ISO 22610:2018 |
Surgical drapes, gowns and clean air suits, used as medical devices, for patients, clinical staff and equipment — Test method to determine the resistance to wet bacterial penetration |
This document specifies a test method, with associated test apparatus, which is used to determine the resistance of a material to the penetration of bacteria, carried by a liquid, when subjected to mechanical rubbing.
|
Published |
2018-09 |
Edition : 2 |
Number of pages : 26 |
Technical Committee |
11.140
Hospital equipment
;
13.340.10
Protective clothing
|
| ISO 22882:2004 |
Castors and wheels — Requirements for castors for hospital beds |
ISO 22882:2004 specifies the technical requirements, the appropriate dimensions and the requirements for testing of swivel castors for hospital beds with a wheel diameter of 100 mm or more, and which have a central locking device. Swivel castors may be used with the main principal dimensions.
|
Withdrawn |
2004-04 |
Edition : 1 |
Number of pages : 12 |
Technical Committee |
11.140
Hospital equipment
|
| ISO 22882:2016 |
Castors and wheels — Requirements for castors for hospital beds |
ISO 22882:2016 specifies the technical requirements, the appropriate dimensions and the requirements for the testing of swivel castors for hospital beds with a wheel diameter of 100 mm or more and which have a central locking device. Swivel castors may be used with the main principal dimensions.
|
Published |
2016-12 |
Edition : 2 |
Number of pages : 11 |
Technical Committee |
11.140
Hospital equipment
|
| IEC 60601-2-52:2009 |
Medical electrical equipment — Part 2-52: Particular requirements for the basic safety and essential performance of medical beds |
IEC 60601-2-52:2009 applies to the basic safety and essential performance of medical beds intended for adults. This first edition cancels and replaces the first edition of IEC 60601-2-38, published in 1996, and its Amendment 1 (1999). This edition constitutes a technical revision. IEC 60601-2-52:2009 is the realization of much work in alignment, and scope adjustment between IEC 60601-2-38, EN 1970, and the third edition of IEC 60601-1.
|
Published |
2009-12 |
Edition : 1 |
Number of pages : 152 |
Technical Committee |
11.140
Hospital equipment
|
| ISO 8670-2:1991 |
Ostomy collection bags — Part 2: Determination of freedom from leakage |
|
Withdrawn |
1991-12 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
11.180
Aids for disabled or handicapped persons
|
| ISO 9999:1992 |
Technical aids for disabled persons — Classification |
|
Withdrawn |
1992-04 |
Edition : 1 |
Number of pages : 28 |
Technical Committee |
11.180
Aids for disabled or handicapped persons
|
| ISO 15562:1998 |
Practice for dosimetry in electron and bremsstrahlung irradiation facilities for food processing |
|
Withdrawn |
1998-12 |
Edition : 1 |
Number of pages : 6 |
Technical Committee |
17.240
Radiation measurements
;
67.020
Processes in the food industry
|
| IEC/TR 60601-4-1:2017 |
Medical electrical equipment — Part 4-1: Guidance and interpretation — Medical electrical equipment and medical electrical systems employing a degree of autonomy |
IEC TR 60601-4-1:2017(E) is intended to help a manufacturer through the key decisions and steps to be taken to perform a detailed risk management and usability engineering processes for medical electrical equipment or a medical electrical system, hereafter referred to as MEE or MES, employing a degree of autonomy (DOA).
This document provides a definition of DOA of MEE or MES and a medical robot, and also provides guidance on:
- methodologies to perform the risk management process and usability engineering for an MEE or MES with a DOA;
- considerations of basic safety and essential performance for an MEE and MES with a DOA; and
- identifying the use of DOA, and similar concepts in existing ISO/IEC standards dealing with MEE or MES with the goal to facilitate alignment of standards by consistent use of the concept of DOA; and
- distinguishing between medical robots, and other MEE and MES.
Unless specified otherwise, this document considers MEE and MES together.
The manufacturer of an MEE or MES with a DOA is expected to design and manufacture an MEE or MES that fulfils its intended use and does not have unacceptable risk throughout its life-cycle.
This document provides guidance to help the manufacturer in complying with the requirements of IEC 60601-1:2005 and IEC 60601-1:2005/AMD1:2012 for MEE and MES with DOA. The document is also intended as guidance for future standard writers.
There are no prerequisites to this document.
|
Published |
2017-05 |
Edition : 1 |
Number of pages : 80 |
Technical Committee |
11.140
Hospital equipment
|
| IEC 60601-2-52:2009/Amd 1:2015 |
Medical electrical equipment — Part 2-52: Particular requirements for the basic safety and essential performance of medical beds — Amendment 1 |
|
Published |
2015-04 |
Edition : 1 |
Number of pages : 15 |
Technical Committee |
11.140
Hospital equipment
|
| IEC 60601-2-52:2009/Cor 1:2010 |
Medical electrical equipment — Part 2-52: Particular requirements for the basic safety and essential performance of medical beds — Technical Corrigendum 1 |
|
Published |
2010-09 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
11.140
Hospital equipment
|
| IEC 60601-2-31:2020 |
Medical electrical equipment — Part 2-31: Particular requirements for the basic safety and essential performance of external cardiac pacemakers with internal power source |
IEC 60601-2-31:2020 applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of EXTERNAL PACEMAKERS powered by an INTERNAL ELECTRICAL POWER SOURCE, hereafter referred to as ME EQUIPMENT. This document applies to PATIENT CABLES as defined in 201.3.209, but does not apply to LEADS as defined in 201.3.206. HAZARDS inherent in the intended physiological function of ME EQUIPMENT within the scope of this document are not covered by specific requirements in this document except in 7.2.13 and 8.4.1 of the general standard. This document does not apply to the implantable parts of ACTIVE IMPLANTABLE MEDICAL DEVICES covered by ISO 14708-1. This document does not apply to EXTERNAL PACEMAKERS which can be connected directly or indirectly to a SUPPLY MAINS. This document does not apply to transthoracic and oesophageal pacing ME EQUIPMENT and antitachycardia ME EQUIPMENT. IEC 60601-2-31:2020 cancels and replaces the second edition published in 2008 and Amendment 1:2011. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the previous edition:
a) The requirement for testing for energy reduction has been removed;
b) The test for exposure to external defibrillation has been completely revised;
c) The exclusion for testing ESD immunity only with respect to air discharges has been removed;
d) Alignment with the latest edition of ISO 14708-2 for pacemakers, as well as the associated EMC standard ISO 14117;
e) Additional rationale for all changes.
|
Published |
2020-01 |
Edition : 3 |
Number of pages : 110 |
Technical Committee |
11.140
Hospital equipment
|
| IEC 80601-2-35:2009 |
Medical electrical equipment — Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads or mattresses and intended for heating in medical use |
IEC 80601-2-35:2009 establishes particular basic safety and essential performance requirements, which minimize hazards to patients, and operators for heating devices using blankets, pads or mattresses and intended for heating in medical use and specifies tests for demonstrating compliance with these requirements. This second edition cancels and replaces the first edition published in 1996. This edition constitutes a technical revision. This new edition provides consistency with the third edition of IEC 60601-1, as well as with the four other particular standards related to paediatric equipment for which the committee is responsible.
|
Withdrawn |
2009-10 |
Edition : 1 |
Number of pages : 124 |
Technical Committee |
11.140
Hospital equipment
|
| IEC 80601-2-35:2009/Amd 1:2016 |
Medical electrical equipment — Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads or mattresses and intended for heating in medical use — Amendment 1 |
|
Withdrawn |
2016-04 |
Edition : 1 |
Number of pages : 10 |
Technical Committee |
11.140
Hospital equipment
|
| IEC 80601-2-35:2009/Cor 1:2015 |
Medical electrical equipment — Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads or mattresses and intended for heating in medical use — Technical Corrigendum 1 |
|
Withdrawn |
2015-02 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
11.140
Hospital equipment
|
| IEC 80601-2-35:2009/Cor 2:2015 |
Medical electrical equipment — Part 2-35: Particular requirements for the basic safety and essential performance of heating devices using blankets, pads or mattresses and intended for heating in medical use — Technical Corrigendum 2 |
|
Withdrawn |
2015-02 |
Edition : 1 |
Number of pages : 1 |
Technical Committee |
11.140
Hospital equipment
|
| ISO/R 168:1960 |
Withdrawal of ISO/R 168-1960 |
|
Withdrawn |
1960-12 |
Edition : 1 |
Number of pages : 4 |
Technical Committee |
11.160
First aid
|
| ISO 4074-2:1994 |
Rubber condoms — Part 2: Determination of length |
Cancels and replaces the first edition (1980). Specifies a method of determining the length of rubber condoms by free hanging of the unrolled condom over a graduated mandrel and measurement of its length, the reservoir excluded.
|
Withdrawn |
1994-11 |
Edition : 2 |
Number of pages : 2 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|
| ISO 4074-3:1980 |
Rubber condoms — Part 3: Determination of width |
|
Withdrawn |
1980-07 |
Edition : 1 |
Number of pages : 1 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|
| ISO 4074-3:1994 |
Rubber condoms — Part 3: Determination of width |
Cancels and replaces the first edition (1980). Specifies a method of determining the width of rubber condoms by free hanging of the unrolled condom over the edge of a ruler and measurement of its width.
|
Withdrawn |
1994-11 |
Edition : 2 |
Number of pages : 1 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|
| ISO 4074-4:1980 |
Rubber condoms — Part 4: Determination of colour fastness |
|
Withdrawn |
1980-06 |
Edition : 1 |
Number of pages : 1 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|
| ISO 4074-5:1980 |
Rubber condoms — Part 5: Testing for holes |
|
Withdrawn |
1980-10 |
Edition : 1 |
Number of pages : 1 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|
| ISO 4074-5:1984 |
Rubber condoms — Part 5: Testing for holes |
|
Withdrawn |
1984-12 |
Edition : 2 |
Number of pages : 1 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|
| ISO 4074-5:1996 |
Rubber condoms — Part 5: Testing for holes — Water leak test |
Describes a method of testing a rubber condom for holes by observing any leakage from the condom after it has been filled with water. Replaces the second edition.
|
Withdrawn |
1996-08 |
Edition : 3 |
Number of pages : 2 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|
| ISO 4074-6:1981 |
Rubber condoms — Part 6: Determination of bursting volume and pressure |
|
Withdrawn |
1981-01 |
Edition : 1 |
Number of pages : 2 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|
| ISO 4074-6:1984 |
Rubber condoms — Part 6: Determination of bursting volume and pressure |
|
Withdrawn |
1984-05 |
Edition : 2 |
Number of pages : 2 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|
| ISO 4074-6:1996 |
Rubber condoms — Part 6: Determination of bursting volume and pressure |
Describes the method of determining the bursting volume and pressure of rubber condoms. Replaces the second edition.
|
Withdrawn |
1996-08 |
Edition : 3 |
Number of pages : 6 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|
| ISO 4074-7:1986 |
Rubber condoms — Part 7: Determination of resistance to deterioration during storage |
|
Withdrawn |
1986-05 |
Edition : 1 |
Number of pages : 1 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|
| ISO 4074-7:1996 |
Rubber condoms — Part 7: Oven conditioning |
Describes a method for the determination of the resistance of packaged condoms to deterioration during storage. Replaces the first edition.
|
Withdrawn |
1996-08 |
Edition : 2 |
Number of pages : 1 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|
| ISO 4074-8:1984 |
Rubber condoms — Part 8: Determination of mass |
|
Withdrawn |
1984-10 |
Edition : 1 |
Number of pages : 1 |
Technical Committee |
11.200
Birth control. Mechanical contraceptives
|