Toimialayhteisöt

 

This document specifies requirements applicable to data and data quality of business transactions, events, measurements and sensor readings. These requirements apply to transaction data in most industrial contexts. The following are within the scope of this document: the different types of transaction data - events, certificates, measurements, sensor readings and business transactions; the nature of transaction data quality; changes to transaction data quality over time; managing transaction data quality. The following are out of scope of this document: the quality and effectiveness of the transaction itself; changes to master data arising from a transaction. NOTE 1 Where the word transaction is used in this standard it refers to "business transaction". NOTE 2 Quality of measurement data and sensor readings is described in more detail in ISO 8000-210:2024 [8], ISO 8000-220[9] and ISO 8000-230. NOTE 3 This standard relates to quality of data about transactions which contributes to the trustworthiness of a transaction, whereas cenelec:proj:82029EN 18235-1:2026 Trusted data transactions - Part 1: Terminology, concepts and mechanismsprEN 18235-2 (WI=JT025008) Trusted Data Transactions - Part 2: Trustworthiness requirements relate to transactions about data and does not conflict with or overlap but benefit from this standard. NOTE 4 ISO/IEC 15944-9:2023 [10] provides useful information about traceability.

 

This document specifies an inspection procedure to be used by the purchaser where no prior agreement exists. It also specifies a reference acceptance procedure for acceptance or rejection of an inspection lot, when no agreement can be reached between the purchaser and the supplier, or where conformance to specification is disputed. It applies to inspection lots of bolts, screws, studs, nuts, pins, washers, rivets and other related fasteners. This document applies to fasteners not intended for high volume machine assembly, special-purpose applications or specially engineered applications requiring more advanced in-process control and lot traceability. For in-process control or final inspection by the manufacture and sorting, see ISO 16426.

 

This document establishes uniform methods for laboratory testing of air curtain units to determine aerodynamic performance in terms of airflow rate, outlet air velocity uniformity, power consumption and air velocity projection, for rating or guarantee purposes. This document does not specify test procedures to be used for design, production or field testing.

 

Tätä standardia sovelletaan kohdan 1.2.6 mukaisten vaarattomien aineiden ja kohdan 1.2.7 mukaisten vaarallisten aineiden vaunusailiöiden ja säiliökonttien tyhjennysasemaan, jossa säiliö tyhjennetään johtamalla siihen paineilmaa tai paineenalaista inerttikaasua, josta seuraavassa käytetään nimitystä PAINEKAASU. Tämä standardi ei koske vaarallisten aineiden kuljetusmääräysten luokkien 1, 2 eikä 7 aineiden tyhjennysasemaa. Tähdellä (*) merkityt standardin kohdat koskevat ainoastaan sellaista tyhjennysasemaa, jossa käsitellään kohdassa 1.2.7 määriteltyä vaarallista ainetta. Ilman tähteä olevat standardin kohdat koskevat sekä vaarallisten että vaarattomien aineiden tyhjennysasemia. Kuljetusvälineeseen sijoitettuihin tyhjennyslaitteisiin, tilapäiseen tyhjennysasemaan sekä siirtokuormaukseen (vaunusäiliöstä tai säiliökontista toiseen) sovelletaan tätä standardia valvontaviranomaisten määräämässä laajuudessa. Lisäksi on kohdassa 6 paineella tyhjennettävän vaunusäiliön ja säiliökontin paineetonta täyttöä koskevia ohjeita.

 

Standardi esitetään kumottavaksi vanhentuneena

SFS:n tehtävänä on ylläpitää ajantasaista suomalaista SFS-standardikokoelmaa.

Tällä lausuntopyynnöllä pyritään selvittämään, tulisiko tämä SFS-standardi kumota vanhentuneena.

Vastaa kohdassa "Ota kantaa", tulisiko tämä SFS-standardi kumota.

(Hyväksyn = hyväksyn tämän standardin kumoamisen vanhentuneena.)

 

This document specifies requirements for the biobanking of human mesenchymal stromal cells derived from umbilical cord tissue (i.e. Wharton’s jelly), further referred to as hUC-MSCs, including the collection of umbilical cord tissue and associated data, isolation, culture characterization, quality control, cryopreservation, storage, thawing, disposal, distribution and transport..This document is applicable to all organizations performing biobanking of hUC-MSCs used for research and development. This document does not apply to hUC-MSCs for the purpose of in vivo application in humans, clinical applications or therapeutic use. NOTE International, national or regional regulations or requirements, or multiple of them, can also apply to specific topics covered in this document.

 

 

This document defines various classifications for the application, rating and performance of generating sets consisting of a Reciprocating Internal Combustion (RIC) engine, Alternating Current (a.c.) generator and any associated controlgear, switchgear and auxiliary equipment. It applies to a.c. generating sets driven by RIC engines for land and marine use, excluding generating sets used on aircraft or to propel land vehicles and locomotives. For some specific applications (e.g. essential hospital supplies, high-rise buildings), supplementary requirements can be necessary. The provisions of this document can be the basis for establishing any supplementary requirements. For other reciprocating-type prime movers (e.g. sewage-gas engines, steam engines), the provisions of this document can be used as a basis for establishing these requirements. Generating sets meeting the requirements of this document are used to generate electrical power for continuous, peak-load and standby applications. The classifications laid down in this document are intended to help understanding between manufacturer and customer.

 

This document specifies minimum requirements for instruments and systems that fall into the class of corneal topographers (CTs). It also specifies tests and procedures to verify that a system or instrument complies with this document and thus qualifies as a CT according to this document. It also specifies tests and procedures that allow the verification of capabilities of systems that are beyond the minimum requirements for CTs. This document defines terms that are specific to the characterization of the corneal shape so that they may be standardized throughout the field of vision care. This document is applicable to instruments, systems and methods that are intended to measure the surface shape of the cornea of the human eye. NOTE The measurements can be of the curvature of the surface in local areas, three-dimensional topographical measurements of the surface or other more global parameters used to characterize the surface. This document is not applicable to ophthalmic instruments classified as ophthalmometers.

 

This document specifies requirements for the biobanking of human mesenchymal stromal cells derived from bone marrow (hBM-MSCs), including the collection of bone marrow and associated data, isolation, culture, characterization, quality control, cryopreservation, storage, thawing, disposal, distribution and transport. This document is applicable to all organizations performing biobanking with hBM-MSCs used for research. This document does not apply to hBM-MSCs for the purpose of in vivo application in humans, cell therapy, clinical applications, tissue engineering or therapeutic use. NOTE International, national or regional regulations or requirements, or multiple of them, can also apply to specific topics covered in this document.

 

This document specifies requirements for empty, sterile, single-use syringe, and needles attached or not to the syringe, intended solely for the withdrawal and injection of fluids of a drug or a substance into an eye or its tissues or into an ocular implantable device. It covers devices intended for single use only that comprises, but not limited to, configurations of co-packaged devices, device kits, syringe with fixed needle, transfer needle, and injection needle, with or without a filter membrane. The syringes are intended to be used immediately after filling and are not intended to store the drug or the substance. This document does not preclude the use of platform delivery systems validated for multiple ophthalmic clinical indications, provided that the device complies with all specific provisions of this standard for its intended intraocular use-case. This document does not specify materials to be used for the construction and lubrication of sterile syringes and needles intended for ophthalmic use because their selection will depend, to some extent, upon the manufacturer’s specific design, process of manufacture, and sterilization method. This document excludes any other application other than ophthalmic tissue injections and excludes syringes which are pre-filled, e.g. pre-filled syringes are covered within ISO 11040 series. Non-invasive route of administration and its drug delivery type of devices like eye droppers or contact lenses are not considered as an injection and therefore out of scope of this document.

 

This document specifies a method that evaluates inactivation/removal effectiveness against airborne microorganisms in air cleaning devices. This method includes detailed requirements for the test rig, and simulates the air flowrate of the devices. The method also covers data acquisition, analysis, and reporting of results. Additionally, this document provides a normative procedure (see Annex A) for determining the effect of dust loading on the inactivation and removal effectiveness. This document is applicable to in-duct air cleaning devices, such as air filters set up in a heating, ventilation and air-conditioning (HVAC) system in commercial, institutional and office buildings, also in-duct air-purifying systems, or air sterilizers in these buildings. It applies to testing conducted under controlled laboratory conditions using specific surrogate test microorganisms (bacteria, moulds and viruses). This document does not apply to — air cleaning devices intended for portable or standalone room use, which are addressed by ISO 16000-36 and the IEC 63086 series, — devices evaluated solely for the physical removal of non-biological particulate matter, which are covered by the ISO 16890 series, and — clinical, medical or industrial cleanroom applications requiring specific pathogenic testing. Furthermore, it does not cover the detailed assessment of ultraviolet (UV) dose evaluation exclusively for in-duct ultraviolet germicidal irradiation (UVGI) devices, which is covered by ISO 15714 and ASHRAE 185.1.

 

This document describes the test method and procedure for the determination of fracture toughness of the physical vapor deposition (PVD) coatings. The test method uses indentation on micropillars fabricated by different techniques, including focused ion beam (FIB) milling, photolithography, and femtosecond laser processing. This test method is applicable to ceramic coatings produced by the PVD technique.

 

This document provides a high-level framework and guidance for the development and operation of conformity assessment schemes, including certification schemes, for artificial intelligence systems (AI systems).

 

The primary objective of this document is to define standard methods to measure three-dimensional relationships between road vehicle foot controls and the enclosing structures such as the floor, sidewalls and lower instrument panel. This standard provides methods for the design or the competitive assessment of the layout, spacing, and clearances between foot controls and their surrounding components. It will include terms and definitions encountered in the design, development and evaluation of foot controls, in both static and dynamic use. This standard also provides guidelines to create requirements for the three-dimensional space between, above, below, and to the side of a foot control system, including use-cases and factors that influence the design of foot controls, such as foot position and foot size based on vehicle type, environmental considerations, and differences between Heavy Trucks and Buses, and Passenger Cars, Sports Utility Vehicles and Light Trucks. This document will include but not be limited to lateral spacing of foot controls (ISO 3409), and will address several deficiencies in ISO 3409, including a modern format with definitions and external references. An addendum will also outline dynamic usability considerations both for manual and semi-autonomous driving, such as the differences between dynamic and static heel points, heel-toe, misapplication, simultaneous push A-B pedals, the effect of driver anthropometry, driver positioning geometry, and design considerations for entry / exit as a function of vehicle type. This standard assumes foot controls of different types for controlling different functions, corresponding both to what exists and will come.

 

This document establishes a methodology for linking abstract concepts within Building Information Modelling (BIM) and Geographic Information System (GIS) standards and specifies structural mechanisms for organizing their link relationships, aiming to facilitate cross-domain information exchange. Methodologies for the development of RDF that relate to BIM and GIS are not within the scope of this document.

 

This document provides a framework of fundamental competences, including proficiency levels, for people in the field of innovation management. The framework describes all the essential knowledge and skill types required to effectively establish, implement, maintain, and continually improve an innovation management system in accordance with ISO 56001. It includes practice competences directly related to innovation management activities and tasks and general competences that are not unique to the field but can be considered within that context. All competences are intended for guidance without prescribing specific tools or methods. This document does not provide job or role definitions, competence development guidance, personal certification requirements, evaluation methodology for the organization, or an innovation management body of knowledge. It does not directly address organizational competences or capabilities.

 

This document specifies a framework of additional characteristics and associated test methods for bitumens and bituminous binders, which is complementary to other product standards for bitumens and bituminous binders. This document is applicable to bitumens and bituminous binders suitable for use in paving applications, but it is also applicable for other uses such as waterproofing membranes. With regard to paving applications, the following characteristics are addressed: - resistance to permanent deformation (rutting); - resistance to low-temperature cracking; - resistance to ravelling; - resistance to fatigue cracking; - temperature susceptibility; - equi-stiffness temperature and phase angle; - durability (evolution of equi-stiffness temperature and phase angle); - mixing and handling characteristics (paving and compaction) temperatures; - additional characteristics (e.g. solubility, elastic recovery and storage stability). Not all the properties and characteristics established in the framework are universally relevant to all binders. For example, elastic recovery is not relevant for unmodified binders.

 

This document specifies a method for measuring the cross-talk of a cable or between cables.

 

This document specifies the determination of whole-body and hand-arm vibration emissions at operator position(s) during testing of mobile machinery. The purpose of this document is to assist technical standardization committees responsible for specific types of machinery in preparing vibration test codes to ensure that such vibration test codes — are as homogeneous as possible with each individual test code having the same basic structure, — are in full accordance with basic standards on measurement of vibration emission, — reflect the latest technical knowledge of methods of determining the vibration emission from the specific family of machinery under consideration, — provide manufacturers with a standardized method for the determination and declaration of the vibration emission value(s) of their machinery, — enable the user of the machinery or the member of an inspection body to compare the vibration emission values of different machinery and to verify the vibration emission values provided by the manufacturer. This document provides requirements for the preparation of vibration test codes (C-type standards), including guidelines for the conditions under which the measurements shall be made (e.g. operating conditions). Information to be included in a typical vibration test code is summarized in Annex A. This document applies to sitting and standing positions. It is applicable to all mobile machinery producing periodic or random vibration with or without transients. This document contains sufficient guidance for designing an appropriate test for machinery for which no vibration test codes exist. It can also be used for the determination of vibration emission values of individual machines. This document is not applicable to rotational vibration and backrest vibration. This document does not present limits or recommended vibration values.

 

This document specifies the chemical composition limits of wrought aluminium and wrought aluminium alloys and form of products. NOTE The chemical composition limits of aluminium and aluminium alloys specified herein are completely identical with those registered with the Aluminium Association, 1525, Wilson Boulevard, Suite 600, Arlington, VA 22209, USA, for the corresponding alloys.