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This document: — describes the functionality of a "local dynamic map" (LDM) in the context of the "bounded secured managed domain" (BSMD); — specifies: — general characteristics of LDM Data Objects (LDM-DOs) that can be stored in an LDM, i.e. information on real objects such as vehicles, road works sections, slow traffic sections, special weather condition sections, which are as a minimum requirement location-referenced and time-referenced; — service access point functions providing interfaces in an ITS station (ITS-S) to access an LDM for: — secure add, update and delete access for ITS-S application processes; — secure read access (query) for ITS-S application processes; — secure notifications (upon subscription) to ITS-S application processes; — management access: — secure registration, de-registration and revocation of ITS-S application processes at LDM; — secure subscription and cancellation of subscriptions of ITS-S application processes; — procedures in an LDM considering: — means for maintaining the content and integrity of the data store; — mechanisms supporting several LDMs in a single ITS station unit.

This part of EN 14960 is applicable to inflatable play equipment intended for use by children fourteen years
and under, both individually and collectively.
This part of EN 14960 specifies additional safety requirements for bungee runs for which the primary
activities are climbing and sliding. It sets measures to address risks and also to minimize accidents to users for those involved in the design, manufacture and supply of inflatable play equipment. It specifies
information to be supplied with the equipment. The requirements have been laid down bearing in mind the
risk factor based on available data.
This part of the EN 14960 specifies requirements to protect a child from hazards that he or she might be
unable to foresee when using the equipment as intended, or in a manner that can be reasonably anticipated.
This part of the EN 14960 is not applicable to inflatable water-borne play and leisure equipment, domestic
inflatable toys, air-supported buildings, inflatables used solely for protection, inflatables used for rescue, or
other types of inflatable toys where the primary activity is not bouncing or sliding.

No scope available

IEC 61558-2-9:2024 is available as IEC 61558-2-9:2024 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.

IEC 61558-2-9:2024 deals with the safety of transformers for class III handlamps and power supply units incorporating transformers for class III handlamps. Transformers incorporating electronic circuits are also covered by this document. This third edition cancels and replaces the second edition published in 2010. This edition constitutes a technical revision.
This edition includes the following significant technical changes with respect to the previous edition:
a) adjustment of structure and references in accordance with IEC 61558-1:2017;
b) addition of a new symbol for power supply unit with linearly regulated output voltage;
c) document is not only valid for transformers for tungsten filament handlamps.
It has the status of a group safety publication in accordance with IEC Guide 104.

IEC 61558-2-8:2024 is available as IEC 61558-2-8:2024 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.

IEC 61558-2-8:2024 deals with the safety of bell and chime transformers and power supply units incorporating bell and chime transformers. Transformers incorporating electronic circuits are also covered by this document. This third edition cancels and replaces the second edition published in 2010. This edition constitutes a technical revision. This edition includes the following significant technical changes with respect to the previous edition:
a) adjustment of structure and references in accordance with IEC 61558-1:2017;
b) new symbol for power supply unit with linearly regulated output voltage.
It has the status of a group safety publication in accordance with IEC Guide 104.

This document specifies the minimum values for expected strength as a function of time and temperature in the form of reference lines, for use in calculations on polyphenylsulfone (PPSU) injection moulded fittings.

This document specifies a method for the determination of total mercury (Hg) in foodstuffs using direct atomic absorption spectrometry after thermal decomposition in an oxygen or air flow and concentration by amalgam formation. The method is applicable for solid and liquid samples.
This method was tested in a collaborative study carried out on seven different materials with a mercury concentration in the range from 0,005 mg/kg to 5,20 mg/kg and successfully validated in this range.
The following foodstuffs were analysed: Saithe (dried); Celery (dried); Wheat noodle powder; Wild mushrooms (dried); Pig liver (dried); Cacao powder; Tuna fish (dried).
The lower limit of the method’s applicability varies depending on the food matrix and the water content of the foodstuff. It is a laboratory-specific value and is defined by the laboratory when calculating the limit of quantification.

This document (FprCEN/TS 12697-51:2024) specifies a test method for measuring the surface shear strength for airfield surface courses.
The surface shear strength will depend on the depth of the surface course together with the properties of the surface course material.
The binder course material and any bonding agent applied between the two layers can have an influence on the test result for, in particular, ultra-thin surface course.

This part of IEC 61189 defines the method to be followed for the determination of the X/Y coefficient of thermal expansion of thin electrical insulating materials via the use of a thermomechanical analyser (TMA). This method is applicable to materials that are solid for the entire range of temperature used, and that retain sufficient rigidity over the temperature range so that so that irreversible indentation of the specimen by the sensing probe does not occur.

This document specifies a method for the assessment of the resistance to cold liquids of all rigid furniture surfaces, regardless of materials. It does not apply to leather and textile surfaces. The test is intended to be carried out on a part of the finished furniture, but can be carried out on test panels of the same material, finished in an identical manner to the finished product, and of a size sufficient to meet the requirements of the test. Annex A includes a selection of suitable test liquids. Annex B provides an example for a testing matrix.

This document specifies the functional requirements and test procedures for an acceleration control for pedal error (ACPE) system. This document applies to the systems installed in light vehicles (category M1 and N1)[2] and it does not apply to those installed in large vehicles or motorcycles.

IEC 61558-2-12:2024 is available as IEC 61558-2-12:2024 RLV which contains the International Standard and its Redline version, showing all changes of the technical content compared to the previous edition.

IEC 61558-2-12:2024 deals with the safety of constant voltage transformers for general applications and power supply units for constant voltage for general applications. Constant voltage transformers incorporating electronic circuits are also covered by this document.
This third edition cancels and replaces the second edition published in 2011. This edition constitutes a technical revision.
This edition includes the following significant technical changes with respect to the previous edition:
a) adjustment of structure and references in accordance with IEC 61558-1:2017;
b) description of constructions moved to IEC 61558-1:2017;
c) new symbol for power supply unit with linearly regulated output voltage.
It has the status of a group safety publication in accordance with IEC Guide 104.

IEC 63522-14:2025 is used for testing along with the appropriate severities and conditions for measurements and tests designed to assess the ability of DUTs to perform under expected conditions of transportation, storage and all aspects of operational use.
This document defines a test for determining the extent to which electrical relays support mould growth and how any mould growth can affect the performance and other relevant properties/functions of a relay.

This document specifies the practical use of the fundamental concepts in ISO 11843 in case of the background noise predominance in instrumental analysis. This document specifies basic methods to — extract the stochastic properties of the background noise, — use the stochastic properties to estimate the SD or CV of the response variable, and — calculate the minimum detectable value based on the SD or CV obtained above. The methods described in this document are useful for checking the detection of a certain substance by various types of measurement equipment in which the background noise of the instrumental output predominates over the other sources of measurement uncertainty. Feasible choices are visible and ultraviolet absorption spectrometry, atomic absorption spectrometry, atomic fluorescence spectrometry, luminescence spectrometry, liquid chromatography and gas chromatography.

This document specifies a procedure for the detection of the DNA transition sequence between the 35S promoter region from cauliflower mosaic virus (P35S) and the neomycin-phosphotransferase gene (nptII) from the Tn5 transposon of Escherichia coli. The P35S-nptII segment is part of a construct which confers resistance to neomycin/kanamycin antibiotics frequently found in genetically modified (GM) plants. The detection method is based on real-time PCR and can be used for qualitative screening purposes. For identification and quantification of a specific GM plant (event) a follow-up analysis has to be carried out. This method is applicable for the analysis of DNA extracted from foodstuffs. It can also be suitable for the analysis of DNA extracted from other products such as feedstuffs and seeds. The application of this method requires the extraction of an adequate amount of amplifiable DNA from the relevant matrix.

This document specifies terms and definitions that are commonly used in the exhibition and event industry. They are grouped into the following five categories: — individual and entity, which lists and classifies the various types of people involved in the exhibition and event industry; — types of event, which defines the different types of exhibitions and events, including physical, hybrid and online exhibitions and events; — related activities, which describes related activities during the exhibition and event; — physical items, which describes the various composition sizes, facilities and types of printed materials of the exhibition and event; and — others.

1.1 This document specifies requirements for the development, validation and routine control of a radiation sterilization process for medical devices. NOTE Although the scope is limited to medical devices, this document can be applicable to other products and equipment. This document covers radiation processes employing irradiators using: a) the radionuclide 60Co or 137Cs; b) a beam from an electron generator; or c) a beam from an X-ray generator. 1.2 This document is not applicable to processes for inactivating viruses or the causative agents of spongiform encephalopathies, such as scrapie, bovine spongiform encephalopathy and Creutzfeldt-Jakob disease. NOTE For information on such processes, see ISO 22442-1, ISO 22442-2, ISO 22442-3, ISO 13022 and ICH Q5A. 1.2.1 This document does not specify requirements for designating a medical device as sterile. NOTE Regional and national requirements can designate medical devices as sterile. See, for example, EN 556-1 or ANSI/AAMI ST67. 1.2.2 This document does not specify a quality management system for the control of all stages of production of medical devices. NOTE It is not a requirement of this document to have a complete quality management system during manufacture, but the elements of a quality management system that are the minimum necessary to control the sterilization process are normatively referenced at appropriate places in the text (see, in particular, REF Section_sec_4 \r \h Clause 4 08D0C9EA79F9BACE118C8200AA004BA90B02000000080000000E000000530065006300740069006F006E005F007300650063005F0034000000 ). Attention is drawn to the standards for quality management systems (see ISO 13485) that control all stages of production of medical devices, including the sterilization process. Regional and national regulations for the provision of medical devices can require implementation of a complete quality management system and the assessment of that system by a third party. 1.2.3 This document does not require that biological indicators be used for validation or monitoring of radiation sterilization, nor does it require that a pharmacopoeial test for sterility be carried out for product release. 1.2.4 This document does not specify requirements for occupational safety associated with the design and operation of irradiation facilities. NOTE Regulations on safety requirements for occupational safety related to radiation can exist in some countries. 1.2.5 This document does not specify requirements for the sterilization of used or reprocessed devices.

This document specifies procedures for DNA extraction from alfalfa (Medicago sativa) seeds and for the specific detection of the herbicide-tolerant alfalfa events J101 and J163 and the lignin-modified alfalfa event KK179 in crop/plant/seed/grain test samples. The detection methods are based on real-time PCR and are targeting the DNA transition sequences between the alfalfa genome and the respective integrated gene construct. The methods can be applied for direct event-specific identification or as a follow-up analysis, if sequences encoding the promoter of the Figwort mosaic virus (P-FMV), the terminator of the nopaline synthase gene from Rhizobium radiobacter (T-nos), or the construct CTP2/CP4-EPSPS (herbicide tolerance) were detected by screening analyses of test samples. In this document, the methods were validated using ground alfalfa seeds and DNA extracted thereof. The PCR methods are also applicable for the analysis of other matrices such as feed and foodstuffs. The application of these PCR methods requires the extraction of an adequate amount of amplifiable DNA from the relevant matrix.