This document provides recommended and other product type names and example pictures of product categories defined in ISO 9999, subclass 09 30, "Absorbing products to contain urine and faeces".

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This document establishes a vocabulary of terms and semantics for all fields of respiratory care involving mechanical ventilation, such as intensive-care ventilation, anaesthesia ventilation, emergency and transport ventilation and home-care ventilation, including sleep-apnoea breathing-therapy equipment. It is applicable
— in lung ventilator and breathing-therapy device standards,
— in health informatics standards,
— for labelling on medical electrical equipment and medical electrical systems,
— in medical electrical equipment and medical electrical system instructions for use and accompanying documents,
— for medical electrical equipment and medical electrical systems interoperability, and
— in electronic health records.
This document is also applicable to those accessories intended by their manufacturer to be connected to a ventilator breathing system or to a ventilator, where the characteristics of those accessories can affect the basic safety or essential performance of the ventilator and ventilator breathing system.
NOTE This document can also be used for other applications relating to lung ventilation, including non-electrical devices and equipment, research, description of critical events, forensic analysis and adverse event (vigilance) reporting systems.
This document does not specify terms specific to breathing-therapy equipment, or to physiologic closed-loop ventilation, high-frequency ventilation or negative-pressure ventilation; nor to respiratory support using liquid ventilation or extra-corporeal gas exchange, or oxygen, except where it has been considered necessary to establish boundaries between bordering concepts.

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The purpose of this standard is to develop uniform nomenclature for the description of forensic dental data
and define a standardized set of uniform terms to convey this information. The goal of the standard is not to
define the extent of information collected, only to be certain that common terms are used in order to aid in an
identifying human remains or a living amnesiac.

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This document contains the terms, definitions, notes to entry and examples corresponding to the frequently used concepts which apply to diagnostic and therapeutic nuclear medicine. It comprises the minimum essential information for each nuclear medicine concept represented by a single term. It provides the reader with the information required to approach this multidisciplinary speciality, such as medical, radiopharmacy and medical physics point of view. It is intended to facilitate communication and promote common understanding.

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    19 pages
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This document defines terms used in dental product standards.
This document aims to facilitate the standard development process and the comprehension of
standards, and to improve communication with the FDI World Dental Federation, the World Health
Organization and other organizations interested in standardization.

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This document defines terms used in dental product standards. This document aims to facilitate the standard development process and the comprehension of standards, and to improve communication with the FDI World Dental Federation, the World Health Organization and other organizations interested in standardization.

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    37 pages
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This document defines terms used to describe external limb prostheses and the wearers of external limb prostheses. NOTE 1 The types of component used in the construction of prostheses are classified and described in the ISO 13405 series. NOTE 2 For the purposes of this document, the abbreviated term ?prosthetics' and its derivatives only apply to external limb prosthetics.

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This document defines general terms used to describe external limb prostheses and orthoses, and the personnel involved in the practice of prosthetics and orthotics. NOTE 1 The complete range of levels of limb amputation are listed and defined in ISO 8549-2. The complete range of classes of orthoses are listed and defined in ISO 8549-3. This document does not apply to breast, ocular or other external prostheses used to replace other parts of the human body, nor to dental prostheses or orthoses. NOTE 2 For the purposes of this document, the abbreviated term 'prosthetics' and its derivatives only apply to external limb prosthetics. The abbreviated term 'orthotics' and its derivatives only apply to external orthotics.

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This document defines terms relating to orthoses. This document does not include terms for orthoses that only encompass limb segments, as these orthoses are limited mainly to use in the treatment of fractures and in sports medicine. NOTE 1 The types of components used in the construction of orthoses are classified and described in ISO 13404. NOTE 2 For the purposes of this document the abbreviated term ?orthotics' and its derivatives only apply to external orthotics.

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This document specifies a vocabulary for the description of surgical limb amputations, amputation procedures, and persons who have had an amputation.

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This document defines terms used in healthcare organization management.

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This document specifies a measuring system for spectacle frames and related vocabulary. It is applicable
to spectacle frames with fronts that are intended to be symmetrical.

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This document defines terms for the theory, technology and methods of Chinese Materia Medica processing. It is not applicable to Kampo medicine.

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This document establishes a vocabulary of terms and semantics for all fields of respiratory care involving mechanical ventilation, such as intensive-care ventilation, anaesthesia ventilation, emergency and transport ventilation and home-care ventilation, including sleep-apnoea breathing-therapy equipment. It is applicable — in lung ventilator and breathing-therapy device standards, — in health informatics standards, — for labelling on medical electrical equipment and medical electrical systems, — in medical electrical equipment and medical electrical system instructions for use and accompanying documents, — for medical electrical equipment and medical electrical systems interoperability, and — in electronic health records. This document is also applicable to those accessories intended by their manufacturer to be connected to a ventilator breathing system or to a ventilator, where the characteristics of those accessories can affect the basic safety or essential performance of the ventilator and ventilator breathing system. NOTE This document can also be used for other applications relating to lung ventilation, including non-electrical devices and equipment, research, description of critical events, forensic analysis and adverse event (vigilance) reporting systems. This document does not specify terms specific to breathing-therapy equipment, or to physiologic closed-loop ventilation, high-frequency ventilation or negative-pressure ventilation; nor to respiratory support using liquid ventilation or extra-corporeal gas exchange, or oxygen, except where it has been considered necessary to establish boundaries between bordering concepts.

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This document establishes the core classification framework for the integration of clinical terms from traditional Chinese medicine (TCM) and Western medicine. This structure supports terminology integration in standardized electronic medical records, including professional clinical terms in TCM and Western medicine. Non-technical terms for electronic medical records are also included.

  • Technical specification
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This document defines terms relating to ophthalmic optics, specifically to blanks, finished spectacle
lenses and fitting purposes.
Terms relating to processes and material for fabrication and surface treatment (other than some specific
terms relating to coatings), and terms relating to defects in materials and after optical processing are
given in ISO 9802.

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This document defines terms relating to ophthalmic optics, specifically to blanks, finished spectacle lenses and fitting purposes.
Terms relating to processes and material for fabrication and surface treatment (other than some specific terms relating to coatings), and terms relating to defects in materials and after optical processing are given in ISO 9802.

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This document defines terms relating to ophthalmic optics, specifically to blanks, finished spectacle lenses and fitting purposes. Terms relating to processes and material for fabrication and surface treatment (other than some specific terms relating to coatings), and terms relating to defects in materials and after optical processing are given in ISO 9802.

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This document defines terms applicable to intraocular lenses, and to the methods used to evaluate them.
NOTE Terms are listed in the alphabetical order of the English terms in the English version of this document.

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This document defines terms applicable to intraocular lenses, and to the methods used to evaluate them.
NOTE Terms are listed in the alphabetical order of the English terms in the English version of this document.

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This International Standard defines terms in the field of sterilization of healthcare products used in the standards developed by ISO/TC 198 "Sterilization of healthcare products", CEN/TC 204 "Sterilization of medical devices", and CEN/TC 102 "Sterilizers and associated equipment for processing of medical devices".

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This document defines terms applicable to intraocular lenses, and to the methods used to evaluate them. NOTE Terms are listed in the alphabetical order of the English terms in the English version of this document.

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IEC 61191-1:2018 is also available as IEC 61191-1:2018 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.
IEC 61191-1:2018 prescribes requirements for materials, methods and verification criteria for producing quality soldered interconnections and assemblies using surface mount and related assembly technologies. This part of IEC 61191 also includes recommendations for good manufacturing processes. This edition includes the following significant technical changes with respect to the previous edition:
- the requirements have been updated to be compliant with the acceptance criteria in IPC‑A-610F;
- the term "assembly drawing" has been changed to "assembly documentation" throughout;
- references to IEC standards have been corrected;
- Clause 9 was completely rewritten;
- Annex B was removed because there are already procedures for circuit board assemblies.

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This document defines terms in the field of the sterilization of health care products including related equipment and processes.

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This document defines terms in the field of the sterilization of health care products including related equipment and processes.

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IEC 60050-871:2018 gives the general terminology used in active assisted living, as well as general terms pertaining to specific applications and associated technologies. This terminology is consistent with the terminology developed in the other specialized parts of the IEV.
It has the status of a horizontal standard in accordance with IEC Guide 108.

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This document identifies and defines the terms applicable to the physical, chemical and optical properties
of contact lenses, their manufacture and uses. It provides a vocabulary of terms and, when appropriate,
the international symbol and abbreviation associated with a specific term. This document also defines
the terms relating to contact lens care products. It also incorporates the classifications of contact lens
materials and gives recommendations for the labelling of the specifications of contact lenses.

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ISO 18369-2:2017 specifies the tolerance limits of the principal optical and physical parameters of rigid corneal, rigid scleral and soft contact lenses at the time of manufacture.
These tolerances might not apply to other purposes, for example, shelf-life studies.

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ISO 18369-1:2017 identifies and defines the terms applicable to the physical, chemical and optical properties of contact lenses, their manufacture and uses. It provides a vocabulary of terms and, when appropriate, the international symbol and abbreviation associated with a specific term. This document also defines the terms relating to contact lens care products. It also incorporates the classifications of contact lens materials and gives recommendations for the labelling of the specifications of contact lenses.

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ISO 18369-1:2017 identifies and defines the terms applicable to the physical, chemical and optical properties of contact lenses, their manufacture and uses. It provides a vocabulary of terms and, when appropriate, the international symbol and abbreviation associated with a specific term. This document also defines the terms relating to contact lens care products. It also incorporates the classifications of contact lens materials and gives recommendations for the labelling of the specifications of contact lenses.

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ISO 18662-1:2017 specifies the basic vocabulary for the Chinese Materia Medica (CMM), including most commonly used CMM species. Each term is provided a Latin name, Chinese name, Pinyin name and English name. Source-related definition of applicable parts and botanical name(s) of the plant, zoological family name of the animal, or mineral stated with mineral or rock title and active ingredients are given as note(s) for each item. ISO 18662-1:2017 is intended to be used by those engaged in the practice and management of production, trade, research and education of crude natural Chinese medicinal materials.

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ISO 19465:2017 specifies a categorial structure within the subject field of traditional Chinese medicine (TCM) clinical practice. It describes the upper-level categories of TCM clinical terms and the nomenclature of the hierarchical categories. It is applicable only to clinical terminological systems in TCM disciplines, not to a comprehensive categorial structure of TCM, the conceptual definition of the hierarchy categories, and terms for individual TCM concepts. The following are considered outside the scope of this document: - comprehensive categories of TCM; - the conceptual definition of the hierarchy categories. - terms for individual TCM concepts; - the terms or categories of Kampo, Korean medicine and other traditional medicines.

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This International Standard establishes a classification and terminology of assistive products,
especially produced or generally available, for persons with disability.
Assistive products used by a person with disability, but which require the assistance of another person
for their operation, are included in the classification.
The following items are specifically excluded from this International Standard:
— items used for the installation of assistive products;
— solutions obtained by combinations of assistive products that are individually classified in this
International Standard;
— medicines;
— assistive products and instruments used exclusively by healthcare professionals;
— non-technical solutions, such as personal assistance, guide dogs or lip-reading;
— implanted devices;
— financial support.

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ISO 9999:2016 establishes a classification and terminology of assistive products, especially produced or generally available, for persons with disability.
Assistive products used by a person with disability, but which require the assistance of another person for their operation, are included in the classification.
The following items are specifically excluded from this International Standard:
- items used for the installation of assistive products;
- solutions obtained by combinations of assistive products that are individually classified in this International Standard;
- medicines;
- assistive products and instruments used exclusively by healthcare professionals;
- non-technical solutions, such as personal assistance, guide dogs or lip-reading;
- implanted devices;
- financial support.

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ISO 29783-3:2016 specifies a method of describing abnormal gait patterns resulting from pathology (excluding prosthetic gait) by identifying the deviations from the normal pattern of gait during each sub-phase of the gait cycle. The description of the deviations includes references to abnormal foot contact and abnormalities of joint motion.

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This International Standard specifies terms, synonyms for terms and definitions used in the process chain for CAD/CAM systems in dentistry.

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ISO 18739:2016 specifies terms, synonyms for terms and definitions used in the process chain for CAD/CAM systems in dentistry.

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ISO 27983-2:2015 specifies a vocabulary for the description of prosthetic gait.

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EN ISO 16443 specifies terms and definitions for dental implants and for instruments, accessories, and the most commonly used clinical terms related to implant systems and procedures in dentistry. Grafting materials and membranes are excluded from this International Standard. The following devices are also excluded from the scope of this International Standard. Device specially designed to be placed within, through or upon the bones of the cranio-facial complex, the primary purpose of which is to provide anchorage for an epithesis (to replace for example: ears, noses and parts of eyes and orbital regions): - epithesis implant; - craniofacial implant; - maxillofacial implant. Device specially designed to be placed within, through or upon the bones of the cranio-facial complex, the primary purpose of which is to provide anchorage for an orthodontic appliance: - orthodontic implant.

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ISO 16443:2014 specifies terms and definitions for dental implants and for instruments, accessories, and the most commonly used clinical terms related to implant systems and procedures in dentistry. Grafting materials and membranes are excluded from ISO 16443:2014.
The following devices are also excluded from the scope of ISO 16443:2014.
Device specially designed to be placed within, through or upon the bones of the cranio-facial complex, the primary purpose of which is to provide anchorage for an epithesis (to replace for example: ears, noses and parts of eyes and orbital regions):
epithesis implant;
craniofacial implant;
maxillofacial implant.
Device specially designed to be placed within, through or upon the bones of the cranio-facial complex, the primary purpose of which is to provide anchorage for an orthodontic appliance:
orthodontic implant.

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IEC 60269-2:2013 provides supplementary requirements for fuses for use by authorized persons and are generally designed to be used in installations where the fuse-links are accessible to, and may be replaced by, authorized persons only. Fuses for use by authorized persons according to the following fuse systems also comply with the requirements of the corresponding subclauses of IEC 60269-1, unless otherwise defined in this standard. This standard is divided into fuse systems, each dealing with a specific example of standardized fuses for use by authorized persons: - Fuse system A: Fuses with fuse-links with blade contacts (NH fuse system), - Fuse system B: Fuses with striker fuse-links with blade contacts (NH fuse system), - Fuse system C: Fuse-rails (NH fuse system), - Fuse system D: Fuse-bases for busbar mounting (NH fuse system), - Fuse system E: Fuses with fuse-links for bolted connections (BS bolted fuse system), - Fuse system F: Fuses with fuse-links having cylindrical contact caps (NF cylindrical fuse system), - Fuse system G: Fuses with fuse-links with offset blade contacts (BS clip-in fuse system), - Fuse system H: Fuses with fuse-links having 'gD' and 'gN' characteristic (class J and class time delay and non time delay fuse types), - Fuse system I: gU fuse-links with wedge tightening contacts, - Fuse system J: Fuses with fuse-links having 'gD class CC' and 'gN class CC' characteristics (class CC time delay and non-time delay fuse types), - Fuse system K: gK fuse-links with blade for bolted connections - High fuse-link ratings from 1 250 A up to 4 800 A (master fuse-links). This fifth edition of IEC 60269-2 cancels and replaces the fourth edition published in 2010. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the previous edition: 1. fuse systems A and B: modified values for the power dissipation of NH aM fuse-links; 2. fuse systems A and B: introduction of dimension r for NH fuse-links; 3. addition of new fuse system K: gK fuse-links with contacts for bolted connections. Key Words: fuse systems A to K, requirements for fuses

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Deals with the safety of hand-held motor-operated or magnetically driven electric tools, the rated voltage of the tools being not more than 250 V for single-phase a.c. or d.c. tools, and 440 V for three-phase a.c. tools. This standard deals with the common hazards presented by hand-held tools which are encountered by all persons in the normal use and reasonably foreseeable misuse of the tools.

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ISO 15883-1:2006 specifies general performance requirements for washer-disinfectors (WD) and their accessories that are intended to be used for cleaning and disinfection of re-usable medical devices and other articles used in the context of medical, dental, pharmaceutical and veterinary practice. It specifies performance requirements for cleaning and disinfection as well as for the accessories which can be required to achieve the necessary performance. The methods and instrumentation required for validation, routine control and monitoring and re-validation, periodically and after essential repairs, are also specified.
The requirements for washer-disinfectors intended to process specific loads are specified in subsequent parts of ISO 15883. For washer-disinfectors intended to process loads of two or more different types the requirements of all relevant parts of this standard apply.
ISO 15883-1:2006 does not specify requirements intended for machines for use for laundry or general catering purposes.
ISO 15883-1:2006 does not include requirements for machines which are intended to sterilize the load, or which are designated as "sterilizers", these are specified in other standards e.g. EN 285.
The specified performance requirements of this standard may not ensure the inactivation or removal of the causative agent(s) (prion protein) of transmissible spongiform encephalopathies.
ISO 15883-1:2006 may be used by prospective purchasers and manufacturers as the basis of agreement on the specification of a WD. The test methods for demonstration of compliance with the requirements of ISO 15883-1:2006 may also be employed by users to demonstrate continued compliance of the installed WD throughout its working life. Guidance on a routine test programme also is given.

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ISO 29783-1:2008 establishes a vocabulary for the description of normal gait.

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    7 pages
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ISO 7176-26:2007 specifies a vocabulary consisting of terms and definitions used in the field of manual and electrically powered wheelchairs (including scooters) and associated seating systems. ISO 7176-26:2007 includes, but is not limited to, the preferred terms used in two or more ISO standards of the ISO 7176, ISO 10542 and ISO 16840 series, but does not include terms considered to be adequately defined in everyday English.

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    41 pages
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This document specifies a measuring system for spectacle frames and related vocabulary. It is applicable to spectacle frames with fronts that are intended to be symmetrical.

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This document defines terms used in dental product standards.
This document aims to facilitate the standard development process and the comprehension of
standards, and to improve communication with the FDI World Dental Federation, the World Health
Organization and other organizations interested in standardization.

  • Standard
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This document establishes a vocabulary of terms and semantics for all fields of respiratory care involving mechanical ventilation, such as intensive-care ventilation, anaesthesia ventilation, emergency and transport ventilation and home-care ventilation, including sleep-apnoea breathing-therapy equipment. It is applicable
— in lung ventilator and breathing-therapy device standards,
— in health informatics standards,
— for labelling on medical electrical equipment and medical electrical systems,
— in medical electrical equipment and medical electrical system instructions for use and accompanying documents,
— for medical electrical equipment and medical electrical systems interoperability, and
— in electronic health records.
This document is also applicable to those accessories intended by their manufacturer to be connected to a ventilator breathing system or to a ventilator, where the characteristics of those accessories can affect the basic safety or essential performance of the ventilator and ventilator breathing system.
NOTE This document can also be used for other applications relating to lung ventilation, including non-electrical devices and equipment, research, description of critical events, forensic analysis and adverse event (vigilance) reporting systems.
This document does not specify terms specific to breathing-therapy equipment, or to physiologic closed-loop ventilation, high-frequency ventilation or negative-pressure ventilation; nor to respiratory support using liquid ventilation or extra-corporeal gas exchange, or oxygen, except where it has been considered necessary to establish boundaries between bordering concepts.

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    146 pages
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ISO 16840-1:2006 applies to seating intended to provide postural support within a wheelchair. It specifies: a global coordinate system that permits the determination and recording of a person's posture while seated in a wheelchair; the standard terms and definitions for use in describing both the posture and the anthropometrics of a person seated in a wheelchair; the terms and definitions for describing the dimensions, location and orientation of seating support surfaces, which together comprise the body support system. ISO 16840-1:2006 does not specify any methods for use in measuring a person's seated posture, nor does it define terms for dynamic physiological movements (such as flexion or extension). ISO 16840-1:2006 might be applicable to seating other than that intended to be used within a wheelchair.

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    77 pages
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