ISO - International Organization for Standardization

This document specifies the commonly used terms in mine haulage.

This document specifies a test procedure for determining the performance of the internal cleaning system fitted onto a sprayer. This document is applicable to mounted, trailed and self-propelled agricultural sprayers used for crop protection and liquid fertilizer applications. It is not applicable to sprayers with direct injection systems, manually operated knapsack sprayers, aircraft sprayers and uncrewed aerial spraying system (UASS).

This document provides a method for quantification of marker peptide of type I collagen which was purified products extracted from bovine tissues with liquid chromatography - tandem mass spectrometry (LC-MS/MS). The method described in this document is intended to be used for marker peptide detection of purified bovine type I collagen which will be used for constructing tissue-engineered medical products (TEMPs) or other collagen-based biomaterials, for product quality control. This method also can be used for qualitative analysis and quantitative detection of bovine-specific and/or type I-specific collagen in the samples mixed with other animal sources and/or other type collagen. This document does not exclude other possible methods for quantifying type I collagen, such as hydroxyproline quantification, that can evaluate the total amount of collagen regardless of type. NOTE 1 The collagen has been known there are greater than 28 types and with the different property in each one. This document focuses on the quantification of marker peptide of purified bovine type I collagen. Type I collagen isolated from skin, tendon, bone, etc., can contain other types of collagen, for example, type III and type V. And type I collagen can be sourced from bovine, swine, etc. For quantification of other types of collagens or type I collagen sourced from other species of animals can use this document as a template, but need to design collagen type-specific or/and animal species-specific characteristic peptides for LC-MS/MS method, as well as optimize the determination conditions. NOTE 2 For quantification of the collagen marker peptide of scaffold which combined with other materials, or type I collagen contained in ECM materials of tissues or type I collagen-based regenerative tissues, can refer to this document, but need to isolate or/and purify the type I collagen with a reasonable and verified method at first (9,10), and then quantify it by referring to the method provided in this document.

Within the general scope described in ISO/IEC 9995-1, this document specifies symbols and methods to distinguish graphic characters which share the same glyph or are represented by similar glyphs on keyboards (including virtual keyboards) and in documentation. Each of these symbols is intended to be considered as universal and non-language related equivalent of names for the function they represent.

This document specifies a test method for determining short-term deformation of a press-fit acetabular component for total hip joint replacement under specific laboratory conditions. This document also defines the conditions of testing so that the important parameters that affect the components are taken into account and it describes how the specimen is set up for testing. The described method is intended to be used to measure the amount of deformation under load and plastic deformation after unloading of various designs and materials used for acetabular components in total hip joint replacement. These measurements are then used in an evaluation of risks associated with acetabular cup deformation for the acetabular component under evaluation to determine if its performance can be adversely affected. In the evaluation of risks associated with acetabular component deformation, it can be useful to take into consideration various design, material and surgical implantation factors (e.g. those identified in REF Section_sec_8 \r \h Clause 8 08D0C9EA79F9BACE118C8200AA004BA90B02000000080000000E000000530065006300740069006F006E005F007300650063005F0038000000 ), and, if necessary, a comparison of results to a reference implant tested under the same conditions. Depending on this evaluation, either additional testing or clinical data, or both, which is outside the scope of this document, can be necessary. The loading of the acetabular components in vivo differs, in general, from the loading defined in this test method. The results obtained here cannot be used to directly predict in vivo performance. This document does not cover methods that examine the test specimens.

This document is applicable to the basic safety and essential performance of sleep apnoea breathing therapy equipment, hereafter referred to as ME equipment, intended to alleviate the symptoms of patients who suffer from obstructive sleep apnoea by delivering a therapeutic breathing pressure to the respiratory tract of the patient. Sleep apnoea breathing therapy equipment is intended for use in the home healthcare environment by lay operators as well as in professional healthcare institutions. Sleep apnoea breathing therapy equipment is not considered to utilize a physiologic closed-loop-control system unless it uses a physiological patient variable to adjust the therapy settings. This document excludes sleep apnoea breathing therapy equipment intended for use with neonates. This document is applicable to ME equipment or an ME system intended for those patients who are not dependent on artificial ventilation. This document is not applicable to ME equipment or an ME system intended for those patients who are dependent on artificial ventilation such as patients with central sleep apnoea. This document is also applicable to those accessories intended by their manufacturer to be connected to sleep apnoea breathing therapy equipment, where the characteristics of those accessories can affect the basic safety or essential performance of the sleep apnoea breathing therapy equipment. Masks and application accessories intended for use during sleep apnoea breathing therapy are additionally addressed by ISO 17510. Refer to Figure AA.1 for items covered further under this document. If a clause or subclause is specifically intended to be applicable to ME equipment only, or to ME systems only, the title and content of that clause or subclause will say so. If that is not the case, the clause or subclause applies both to ME equipment and to ME systems, as relevant. Hazards inherent in the intended physiological function of ME equipment or ME systems 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. NOTE 2 See also 4.2 of the general standard. This document does not specify the requirements for: – ventilators or accessories intended for critical care ventilators for ventilator-dependent patients, which are given in ISO 80601‑2‑12. – ventilators or accessories intended for anaesthetic applications, which are given in ISO 80601-2-13. – ventilators or accessories intended for home care ventilators for ventilator-dependent patients, which are given in ISO 80601-2-72. – ventilators or accessories intended for emergency and transport, which are given in ISO 80601-2-84. – ventilators or accessories intended for home-care ventilatory support, which are given in ISO 80601‑2-79 and ISO 80601‑2‑80. – high-frequency ventilators[23], which are given in ISO 80601-2-87. – respiratory high flow equipment, which are given in ISO 80601‑2‑90; NOTE 3 ISO 80601-2-80 ventilatory support equipment can incorporate high-flow therapy operational mode, but such a mode is only for spontaneously breathing patients. – user-powered resuscitators, which are given in ISO 10651-4; – gas-powered emergency resuscitators, which are given in ISO 10651-5; – oxygen therapy constant flow ME equipment; and – cuirass or “iron-lung” ventilation equipment.

This document specifies three procedures, A, B and C, using the Pensky-Martens closed cup tester, for determining the flash point of combustible liquids, liquids with suspended solids, liquids that tend to form a surface film under the test conditions, biodiesel and other liquids in the temperature range of 40 °C to 370 °C. NOTE 1 Although, technically, kerosene with a flash point above 40 °C can be tested using this document, it is standard practice to test kerosene according to ISO 13736.[ REF Reference_ref_9 \r \h 5 08D0C9EA79F9BACE118C8200AA004BA90B0200000008000000100000005200650066006500720065006E00630065005F007200650066005F0039000000 ] Similarly, lubricating oils are normally tested according to ISO 2592.[ REF Reference_ref_6 \r \h 2 08D0C9EA79F9BACE118C8200AA004BA90B0200000008000000100000005200650066006500720065006E00630065005F007200650066005F0036000000 ] Procedure A is applicable to distillate fuels (diesel, biodiesel blends, heating oil and turbine fuels), new and in-use lubricating oils, paints and varnishes, and other homogeneous liquids not included in the scope of procedures B or C. Procedure B is applicable to residual fuel oils, cutback residuals, used lubricating oils, mixtures of liquids with solids, and liquids that tend to form a surface film under test conditions or are of such kinematic viscosity that they are not uniformly heated under the stirring and heating conditions of procedure A. Procedure C is applicable to fatty acid methyl esters (FAME) as specified in specifications such as EN 14214[ REF Reference_ref_15 \r \h 11 08D0C9EA79F9BACE118C8200AA004BA90B0200000008000000110000005200650066006500720065006E00630065005F007200650066005F00310035000000 ] or ASTM D6751.[ REF Reference_ref_17 \r \h 13 08D0C9EA79F9BACE118C8200AA004BA90B0200000008000000110000005200650066006500720065006E00630065005F007200650066005F00310037000000 ] This document is not applicable to water-borne paints and varnishes. NOTE 2 Water-borne paints and varnishes can be tested using ISO 3679.[3] Liquids containing traces of highly volatile materials can be tested using ISO 1523[1] or ISO 3679.

This document specifies methods for the olfactory and visual examination and determination of foreign matter and defects in green coffee from all origins. These methods can also be used for determining one or more of the characteristics of green coffee with an impact on coffee quality for technical, commercial, administrative and arbitration purposes, and for quality control or quality inspection. This document is applicable to green coffee as defined in ISO 3509.

This document specifies a test procedure to simulate and to evaluate lumbar and cervical spinal disc prostheses wear under adverse impingement conditions.

This document provides a list of recommended ISO cryptographic algorithms for use within applicable ISO TC 68, Financial services, standards. It also provides strategic guidance on key lengths and associated parameters and usage dates. This document focuses on core algorithms, key lengths and frequently used mechanisms. The included algorithms are considered to be fit for purpose for financial service use. For additional algorithms, see the body of standards produced by ISO/IEC JTC 1 SC 27, Information security, cybersecurity and privacy protection. For standards on key management, see ISO 11568. The categories of algorithms covered are: a) block ciphers and modes of operation; b) stream ciphers; c) message authentication codes (MACs); d) authenticated encryption algorithms; e) format preserving encryption; f) hash functions; g) asymmetric algorithms: 1) digital signature schemes giving message recovery; 2) digital signatures with appendix; 3) asymmetric ciphers. h) authentication mechanisms; i) key derivation, establishment and agreement mechanisms; j) key transport mechanisms: 1) key wrapping. This document does not define any cryptographic algorithms. However, the standards to which this document refers contain necessary implementation information as well as more detailed guidance regarding choice of security parameters, security analysis and other implementation considerations.

This document applies to force-controlled thermo-mechanical fatigue (TMF) testing. Both forms of control, force or stress, can be applied according to this document. This document describes the equipment, specimen preparation, and presentation of the test results to determine TMF properties.

This document is limited to the evaluation of toner cartridge page yield for toner-containing cartridges (i.e. all-in-one toner cartridges and toner cartridges without a photoconductor) for colour electrophotographic print systems. This document can also be applied to the printer component of any multifunctional device that has a digital input printing path, including multi-function devices that contain electrophotographic printer components. This document is only intended for the measurement of toner cartridge page yield when printing on plain paper using cyan, magenta, yellow and black toner cartridges. No other claims can be made from this testing regarding quality, reliability, etc. This document is not for use with printers whose minimum printable size is equal to or greater than A3 or for photo-only printers. Application of this document for yield measurement of toner replenishment systems (i.e. toner cartridge and bottle type systems where the toner reservoir is internal to the printing system and not user-replaceable) implies some procedural modifications specifically noted herein. This document is intended for equipment used in the office space and does not apply to production volume or large format printing machines where the major cost of ownership is not caused by the consumable yield measured in this document. NOTE 1 An all-in-one toner cartridge is a cartridge that includes at least: a toner containment part, a photoreceptor part and a developer part (see ISO/IEC 29142-1). NOTE 2 This document will be used for the measurement of one of the contributions to cost per page (CPP). This document does not directly measure CPP, only the yield of the magenta, cyan, yellow and black toner cartridges. In most cases, these are not the only contributors to the CPP. It is beyond the scope of this document to provide a methodology for calculation of CPP.

This document describes the general principles of train detection for operations and services which are applied to any railway. This document provides the link of train detection with management of operational principles. It includes descriptions of operational and environmental conditions affecting train detection and impacts on operations. This document provides non-technical guidance for supporting the choice of a suitable train detection method relating to railway operations, for new lines and upgrade or renewal of train detection systems. This document excludes all technical aspects.

This document is limited to the evaluation of toner cartridge page yield for toner containing cartridges (i.e. all-in-one toner cartridges and toner cartridges without a photoconductor) for monochrome electrophotographic print systems. This document can also be applied to the printer component of any multifunctional device that has a digital input-printing path, including multi-function devices that contain printer components. This document is only intended for the measurement of toner cartridge yield. No other claims may be made from this testing regarding quality, reliability, etc. This document is not for use with printers whose minimum printable size is equal to or greater than A3 or for photo-only printers. Application of this document for yield measurement of toner replenishment systems (i.e. toner cartridge- and bottle-type systems where the toner reservoir is internal to the printing system and not user-replaceable) implies some procedural modifications specifically noted herein. This document is intended for equipment used in the office space and does not apply to production volume or large format printing machines where the major cost of ownership is not caused by the consumable yield measured in this document. NOTE 1 An all-in-one toner cartridge is a cartridge that includes at least a toner containment part, a photoreceptor part and a developer part (see ISO/IEC 29142-1). NOTE 2 This document can be used for the measurement of one of the contributions to cost per page (CPP). This document does not directly measure CPP, only the yield of the toner cartridges. In most cases, these are not the only contributors to the CPP. It is beyond the scope of this document to provide a methodology for calculation of CPP.

This document provides reference software for Rec. ITU-T H.266 | ISO/IEC 23090-3. The reference software includes both encoder and decoder functionality. Reference software is useful in aiding users of a video coding standard to establish and test conformance and interoperability, and to educate users and demonstrate the capabilities of the standard. For these purposes, the accompanying software is provided as an aid for the study and implementation of Rec. ITU-T H.266 | ISO/IEC 23090-3.

This document establishes a general classification of jib cranes and their mechanisms based on the service conditions, expressed by the following: — the total number of working cycles to be carried out during the specified design life of the jib crane; — the load spectrum factor which represents the relative frequencies of loads to be handled; — the average displacements.

This document provides guidelines for establishing, maintaining, monitoring and improving infrastructure resilience to help ensure the continuity and robustness of essential services. It supports collaborative decision-making across many stakeholders in diverse organizations. It can be used for engaging stakeholders at all levels responsible for, or having influence on, infrastructure resilience matters. This document is intended to be applicable to all types and sizes of organizations which have a role in infrastructure resilience.

This document specifies the requirements for the bar code symbology known as EAN/UPC. This document specifies EAN/UPC symbology characteristics, data character encodation, dimensions, tolerances, decoding algorithms and parameters to be defined by applications. It specifies the symbology identifier prefix strings for EAN/UPC symbols. Data content and the rules governing the use of this symbology are outside the scope of this document; they are defined in GS1 General Specifications.

Within the general scope described in ISO/IEC 9995-1, this document specifies the numeric section of a keyboard and the division of that section into zones. It specifies the arrangement, the number and the location of the keys in the numeric zone ZN0 and in the function zone ZN1 of the numeric section, as well as the allocation of functions to the keys. The numeric zone ZN0 is to be used in keyboards for applications such as text and data processing, general office environment, banking, point of sales (POS), telematic services, telephony apparatus, home electronic systems, numerical control of machinery and equipment, input of personal identification number (PIN), etc. The function zone ZN1 is to be used in keyboards for applications such as data entry, text and data processing, general office environment, etc. NOTE Certain of these applications are under the responsibility of the ITU-T.

This document provides the specialized requirements for individuals to demonstrate competence in performing IT product security evaluations and reviews according to the ISO/IEC 15408 series and ISO/IEC 18045. NOTE It is possible that evaluators and testers belong to bodies operating under ISO/IEC 17025 and reviewers belong to bodies operating under ISO/IEC 17065.

This document specifies a test method to assess ductility of the fusion joint interface of polyethylene electrofusion socket assemblies for use in pipe systems for the distribution of fluids. This method is applicable to assemblies, with nominal outside diameters greater than or equal to 90 mm.

This document establishes an organized set of concepts and relationships to understand the competency requirements for information security conformance-testing and evaluation specialists, thereby establishing a basis for shared understanding of the concepts and principles central to the ISO/IEC 19896 series across its user communities.

This document establishes a framework to support stakeholders in supply and value chains to ensure the chain of trustworthiness regarding the properties of their products and production processes. This document provides guidelines to identify information relevant to trustworthiness to be exchanged between supply and value chain stakeholders. It also provides an interoperable data structure that is required for supply and value chain stakeholders to negotiate and exchange information relevant to trustworthiness. The guidelines set out in this document are generic and are intended to be applicable to all organizations and products, regardless of type, size or nature.

This document gives guidance on sample preparation, and on qualitative and quantitative determination of elements in particulate matter collected on filtering membranes (PM filter) by energy dispersive X-ray Fluorescence (EDXRF) in different geometrical configurations. This document does not apply to PM filter sampling. This document only applies to the analysis of X-ray emission from filters that are probed using an X-ray beam as the exciting source. X-ray emissions generated by electron microscope are excluded[1]. This document is applicable under a range of contexts including, but not limited to, those highlighted in the introduction. The described method is generally applicable for the determination of elements with atomic number higher than 11 (Na) and having a deposited mass on the filter greater than 10 ng. The elements that can be identified and the detection limits depend on the specific instrumental configuration employed. Various types of filtering membranes (filter) materials can be used, such as glass fibre, quartz fibre, cellulose, nylon, polycarbonate (PC) and polytetrafluoroethylene (PTFE). The entire filter, or portions of various sizes thereof, can be submitted for analysis. NOTE Reference free analysis, based on fundamental parameters is excluded, as the nature of the PM filter samples means that the parameters are not sufficiently well defined.

This document specifies requirements for the design, construction and operation of platform barrier systems positioned at the edge of a station platform immediately adjacent to the rail or other guided vehicles in stations and boarding points for passenger services. This document includes: — requirements for the fixed structure and fixed parts along the platform; — physical requirements for the movable doors and gates normally used by passengers; — requirements for emergency doors; — requirements for driver access doors; — requirements for platform extremity doors; and — requirements for the management of safety risks that are particular to barrier systems. NOTE This document provides requirements for doors and gates on conventional panel construction from platform level to the top of the door, or gate. This document also gives requirements for the integration of barriers within the overall rail system, including: — synchronization of vehicle and platform barrier doors/gates; — audible and visible alerts; — integrity of control systems; — testing of the barrier installation; — operational performance; and — requirements relating to other interfacing sub-systems, notably signalling and vehicles. This document does not cover barrier systems set back from the platform edge, which are used to control access to trains or for crowd management, however, relevant sections of the document can be used as guidance. This document applies to rail services, e.g. metro, tram systems and main line railway system services as requested by a project specification. It applies to small systems, working in conjunction with a single vehicle, or with larger systems working with a complete train. This document applies to platform barrier systems used at sub-surface stations, enclosed surface stations (e.g. those enclosed for the purposes of providing an air-conditioned environment for waiting passengers), and those fully in the open-air. This document applies to all persons involved in the implementation and system integration of a platform barrier system, including infrastructure owners, designers, installers and operators. This document does not cover barrier systems using doors/gates that utilize multiple panels, bars, ropes, etc. or which operate in a vertical direction. This document does not cover requirements: — relating to fire performance or fire requirements arising from use of platform barrier systems as fire barriers; or — for platforms, or other foundations and structures to which the barrier system is secured.

This document describes the architecture of systems for the internet of media things. It also includes a comprehensive set of use cases that can be deployed on such an architecture.

This document specifies the requirements and general principles governing the biological evaluation of medical devices within a risk management process according to ISO 14971. This document applies to the biological evaluation of medical devices that have direct contact or indirect contact with either: — a patient's body during intended use or reasonably foreseeable misuse; or — the body of other users who are not patients, if the medical device is intended for personal protection (e.g. medical gloves, surgical masks). Biological evaluation assesses the biological safety of the medical device by considering the biological risks associated with: — constituents of a medical device; and — tissue-device interactions (including physical effects). The biological evaluation specified in this document can address the biological safety of the medical device, considering the life cycle from design and development through initial use of the finished medical device to final decommissioning or withdrawal from use. The biological evaluation considers both the biological safety of the finished device in first use, and the significance of any changes to the medical device which can occur throughout the life cycle. However, the evaluation of risks related to environmental impacts of decommissioning of medical devices are not within the scope of this document. This document does not mandate re-testing of medical devices that are already on the market and have established and acceptable safety profiles (see REF Section_sec_6.6.2 \r \h 6.6.2 08D0C9EA79F9BACE118C8200AA004BA90B020000000800000012000000530065006300740069006F006E005F007300650063005F0036002E0036002E0032000000 ). This document can be useful to support clinical or usability evaluations of medical devices. For example, a biological evaluation is a pre-requisite for conducting a clinical trial. This means that principles outlined in this document can be applied to the evaluation of prototype or development stage devices, as well as to finished medical devices. Other parts of the ISO 10993 series cover specific aspects of biological evaluation, such as chemical characterization, biological testing, sample preparation, animal welfare and toxicological risk assessment. For some types of medical devices, specific requirements from other standards (outside the ISO 10993 series) can be considered with a justification for the approach taken if there are differences between the requirements of the ISO 10993 series and those provided in other standards. For example, the ISO 18562 series provides specific requirements for biological evaluation of breathing gas pathway medical devices and ISO 7405 provides specific requirements for biological evaluation of dental devices. The evaluation of risks related to infectious agents [e.g. bacteria, moulds, yeasts, viruses, transmissible spongiform encephalopathy (TSE) agents] is not within the scope of this document. NOTE 1 The evaluation of bacterial endotoxins is addressed by ISO 11737-3. NOTE 2 The evaluation of risks related to viruses, TSE agents and other pathogens originating from materials of animal origin is addressed by the ISO 22442 series.

This document provides the findings of a global, country-based survey on the current state, challenges and need for standardization in secondary use of clinical genomics data in medicine. This document excludes the primary use of clinical genomics data as well as specific data, metadata, or policies regarding the secondary use of clinical genomics data.

This document specifies a procedure to determine the slip factor of faying surfaces in slip-resistant (friction) connections to be used in structural steelwork. The method is mainly applicable to uncoated and coated components made of steel with various surface treatments. This document applies mainly to carbon steels but can be used for other type of steels as appropriate.

This document provides guidelines for the management of centralized water reuse systems and water reuse applications in urban areas. This document addresses centralized water reuse systems in their entirety and is applicable to any water reclamation system component (e.g. source water, treatment, storage, distribution, operation and maintenance and monitoring). This document provides: — principles and methodology of reclaimed water management; — management issues in each system component of a centralized water reuse system; — water quality monitoring; — specific aspects for consideration and emergency response. This document excludes monitoring parameters and regulatory values (e.g. water quality limits) of a centralized water reuse system.

This method gives a standardized procedure for the conditioning operation when selecting a conditioning product at laboratory scale and also for the production of flocculated thickened sludge for subsequent dewatering tests. This document provides a method for laboratory chemical conditioning of sludge. The method applies to sludges and suspensions from: — storm water handling; — urban wastewater collecting systems; — urban wastewater treatment plants; — industrial wastewater that has been treated similarly to urban wastewater; — water supply plants. This document is applicable to all sludge that can have similar environmental or health impacts, or both, with exclusion of hazardous sludge from industry and dredged sludge.

This document provides management guidelines to the organizational profile specified in ISO/IEC 29110-4-2 through organizational management, product portfolio management, resource management and process management processes. This document applies to VSEs that develop software or works thru operating processes. This document is intended to be used with any processes, techniques and methods that enhance the VSEs’ customer satisfaction and productivity.

This document specifies a method for the determination of the gas-transmission rate of any plastic material in the form of film, sheeting, laminate, co-extruded material or flexible plastic-coated material. Specific examples, currently in use, of the method are described in the annexes.

This document specifies the operating procedures for chicken slaughtering.

This document addresses the specification and demonstration of capability and system reliability to successfully deliver a medicinal product as part of design verification and manufacture, utilizing empirical methods as well as modelling. This includes risk-based techniques to establish and demonstrate the required reliability level for all disposable single use drug delivery systems (DDSs) for which there is a single opportunity to deliver a single dose of a medicinal product. DDSs covered by this document include, but are not limited to: — needle-based injection systems (ISO 11608-1); — needle-free injection systems (ISO 21649); — aerosol drug delivery systems (ISO 20072). This document does not cover: — DDSs with containers that can be replaced; — DDSs intended for dental use; — finished needles; — empty syringes; — catheters; — DDSs for multi-patient use; — pumps [IEC 60601-2-24 (if electronic) or ISO 28620 (if non-electronic)]; — stand-alone prefilled syringes defined by ISO 11040-8. In this document system reliability is limited to assessing functional performance of the DDS and does not address human factors or user interface considerations. These will be covered by a usability engineering program in accordance with IEC 62366-1. NOTE DDSs not in scope of this document can still benefit from elements in this document but provisions of this document might not completely fulfil the basic safety and effectiveness of such DDSs.

This document provides guidelines for the planning and design of centralized water reuse systems and water reuse applications in urban areas. This document addresses centralized water reuse systems in their entirety and is applicable to any water reclamation system component (e.g. source water, treatment, storage, distribution, operation and maintenance and monitoring). This document provides: — system components and possible models of a centralized water reuse system; — design principles of a centralized water reuse system; — common assessment criteria and related examples of water quality indicators, all without setting any target values or thresholds; — specific aspects for consideration and emergency response. This document excludes design parameters and regulatory values of a centralized water reuse system.

This document specifies test methods for determining the conformance of radio frequency identification (RFID) devices (tags and interrogators) for item management with the specifications given in ISO/IEC 18000-61, ISO/IEC 18000-62 and ISO/IEC 18000-64. However, this document does not apply to the testing of conformance with regulatory or similar requirements. The test methods require only that the mandatory functions, and any optional functions which are implemented, are verified. This can, in appropriate circumstances, be supplemented by further, application-specific functionality criteria that are not available in the general case. The interrogator and tag conformance parameters in this document are the following: — type-specific conformance parameters including nominal values and tolerances; — parameters that apply directly affecting system functionality and inter-operability. Parameters that are already included in regulatory test requirements are not included in this document. Unless otherwise specified, the tests in this document are intended to be applied exclusively to RFID tags and interrogators defined in ISO/IEC 18000-61, ISO/IEC 18000-62 and ISO/IEC 18000-64.

This document defines concepts or unification of concepts for lithium minerals, lithium metals, lithium compounds, lithium alloys, and lithium scrap recycling, including concepts related to materials characteristics, physical characteristics, and chemical characteristics. This document can be used as a reference for concepts and unified concepts in lithium minerals, compounds, alloys and scrap recycling production, application, inspection, circulation, trading, scientific research and education purposes.

This document specifies particular requirements for portable units which are part of a transportable liquid oxygen system and used to provide a controlled flow of oxygen for inhalation by the patient in the home-care environment. Portable units are intended to be used without professional supervision, carried by patients while moving around and during their off-site activities and refilled from a base unit via a transfilling device through the portable unit’s filling port connector. NOTE Requirements that are common to both portable units and base units are specified in ISO 18777-1.

This document specifies how a welding procedure specification (WPS) for production welding of steel castings is qualified. Tests are intended to be carried out in accordance with this document, unless additional tests are specified by the purchaser or by agreement between the contracting parties. This document defines the conditions for the execution of welding procedure qualification tests and the limits of validity of a qualified welding procedure for all practical welding operations within the range of essential variables. This document applies to the arc welding of steel castings. The principles of this document can be applied to other fusion welding processes subject to agreement between the contracting parties.

This document specifies a basic measurement method by using the variable temperature sealed housing for evaporative determination (VT-SHED) test procedure for evaporative emissions from motorcycles. It is applicable to motorcycles equipped with a spark ignition engine (four-stroke engine, two-stroke engine or rotary piston engine).

This document specifies test methods applicable to fibre-reinforced polymer (FRP) sheets for the upgrading of concrete members.

This document specifies the principles, instruments, materials and experimental conditions for testing Young’s modulus and Poisson’s ratio using triaxial testing method. It also specifies the sampling and mechanical testing procedures, as well as the method and precision requirements for calculating shale mechanical brittleness index based on Young’s modulus and Poisson’s ratio. This document is applicable to reservoir quality evaluation and sweet spot identification in shale gas production.

This document specifies data elements and data frames for messages a) exchanged between roadside modules and: 1) signal controllers; 2) traffic management centres, and/or; 3) other roadside modules. b) exchanged between traffic management centres and signal controllers. This document addresses the data in the application layer of the OSI (Open Systems Interconnection) reference model.

This document defines minimum specific elements required for BIM process with new lifts. It does not define the BIM process itself. This document specifies a minimum set of information for lifts following the structure of ISO 7817-1, for the purpose of building planning during pre-design stage, schematic design stage and detailed design stage of a building. It covers the geometrical information and the alphanumerical information. NOTE The BIM processes are defined in ISO/TC 59/SC 13 standards. This document does not cover requirements during other stages (information delivery milestones) and the documentation. This document does not cover definition of actors, which are project specific. The definitions are for a single lift. This document does not describe the structures required for multiple lifts in the same building. This document describes the information of a lift and its interfaces to the building which are relevant for the planning of the building. The structural forces are out of the scope of this document. This document is not applicable to lifts, which are installed before the date of its publication.

This document specifies the conditions for determination of the tensile properties of single filaments of ceramic fibre such as the tensile strength, Young modulus and fracture strain. This document applies to continuous ceramic filaments taken from tows, yarns, braids and knittings, which have strain to fracture less than or equal to 5 %. This document does not apply to carbon fibres that exhibit a nonlinear stress-strain curve. This document does not apply to checking the homogeneity of strength properties of fibres, or to assessing the effects of volume under stress. Methods of estimation of strength statistical parameters are indicated.