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prEN IEC 62841-4-12:2026 Public enquiry
Comment end date 2026-08-19
Electric motor-operated hand-held tools, transportable tools and lawn and garden machinery - Safety - Part 4-12: Particular requirements for robotic lawnmowers
prEN 16002 Public enquiry
Comment end date 2026-08-25
Flexible sheets for waterproofing - Determination of the resistance to wind load of mechanically fastened flexible sheets for roof waterproofing

This document specifies a test method to determine the resistance to wind load of mechanically fastened flexible sheets for roof waterproofing. The assessment is limited to the performance of the mechanically fastened flexible sheets only. The test method does not include the determination of the performance of the fixing element and the mechanical fastener in combination with the structural deck.

prEN IEC 60335-2-50:2026/prA1:2026 Public enquiry
Comment end date 2026-09-09
Household and similar electrical appliances - Safety - Part 2-50: Particular requirements for commercial electric bains-marie

This European Standard deals with the safety of electrically operated commercial bainsmarie not intended for household and similar use, their rated voltage being not more than 250 V for single-phase appliances connected between one phase and neutral, and 480 V for other appliances

prEN 304 618 V0.2.2 (2026-06) Public enquiry
Comment end date 2026-09-14
Cyber Security (CYBER); CRA; Cybersecurity requirements for password managers
ISO/DIS 13682-1 Public enquiry
Comment end date 2026-08-15
Laser and laser related equipment — Determination of the properties of ultrashort laser pulses — Part 1: Vocabulary and symbols
prEN 16256 Public enquiry
Comment end date 2026-08-18
Pyrotechnic articles - Theatrical pyrotechnic articles

This document defines various terms relating to the design, construction, primary packaging and testing of theatrical pyrotechnic articles and specifies their generic types. It defines the procedures for placing generic types, subtypes or individual items of theatrical pyrotechnic articles into the appropriate Categories, T1 or T2 and lists them. It specifies minimum labelling requirements for the article and primary packaging and for the instructions for use. Specific test methods for theatrical pyrotechnic articles of the generic types are defined.

ISO 20109:2025/DAmd 1 Public enquiry
Comment end date 2026-09-12
Simultaneous interpreting — Equipment — Requirements — Amendment 1
prEN 301 721 V2.2.0 (2026-07) Public enquiry
Comment end date 2026-09-20
Satellite Earth Stations and Systems (SES); Mobile Earth Stations (MES) providing Low Bit Rate Data Communications (LBRDC) using Low Earth Orbiting (LEO) satellites operating below 1 GHz frequency band; Harmonised Standard for access to radio spectrum
prEN ISO 25178-70 Public enquiry
Comment end date 2026-08-20
Geometrical product specification (GPS) - Surface texture: Areal - Part 70: Material measures (ISO/DIS 25178-70:2026)

ISO 25178-70:2014 specifies the characteristics of material measures used for the periodic verification and adjustment of areal surface texture measurement instruments.

prEN ISO 22882 Public enquiry
Comment end date 2026-08-25
Castors and wheels - Requirements for swivel castors for hospital beds (ISO/DIS 22882:2026)

ISO 22882:2016 specifies the technical requirements, the appropriate dimensions and the requirements for the testing of swivel castors for hospital beds with a wheel diameter of 100 mm or more and which have a central locking device. Swivel castors may be used with the main principal dimensions.

prEN 300 019-1-2 V3.1.0 (2026-06) Public enquiry
Comment end date 2026-09-14
Environmental Engineering (EE); Environmental conditions and environmental tests for telecommunications equipment; Part 1: Classification of environmental conditions; Subpart 2: Transportation
prEN ISO 10993-4 Public enquiry
Comment end date 2026-09-03
Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO/DIS 10993-4:2026)

ISO 10993-4:2017 specifies general requirements for evaluating the interactions of medical devices with blood. It describes a) a classification of medical devices that are intended for use in contact with blood, based on the intended use and duration of contact as defined in ISO 10993‑1, b) the fundamental principles governing the evaluation of the interaction of devices with blood, c) the rationale for structured selection of tests according to specific categories, together with the principles and scientific basis of these tests. Detailed requirements for testing cannot be specified because of limitations in the knowledge and precision of tests for evaluating interactions of devices with blood. This document describes biological evaluation in general terms and may not necessarily provide sufficient guidance for test methods for a specific device. The changes in this document do not indicate that testing conducted according to prior versions of this document is invalid. For marketed devices with a history of safe clinical use, additional testing according to this revision is not recommended.

prEN ISO 1628-2 Public enquiry
Comment end date 2026-08-25
Plastics - Determination of the viscosity of polymers in dilute solution using capillary viscometers - Part 2: Poly(vinyl chloride) resins (ISO/DIS 1628-2:2026)

1.1 This document specifies conditions for the determination of the reduced viscosity (also known as viscosity number) and K-value of PVC resins. It is applicable to resins in powder form which consist of homopolymers of the monomer vinyl chloride and copolymers, terpolymers, etc., of vinyl chloride with one or more other monomers, but where vinyl chloride is the main constituent. The resins can contain small amounts of unpolymerized substances (e.g. emulsifying or suspending agents, catalyst residues, etc.) and other substances added during the course of the polymerization. This document is not applicable, however, to resins having a volatile-matter content in excess of 0,5 % ± 0,1 %, when determined in accordance with ISO 1269:2006. In addition to this, it is not applicable to resins which are not entirely soluble in cyclohexanone. 1.2 The reduced viscosity and K-value of a particular resin are related to its molecular mass, but the relationship varies depending on the concentration and type(s) of other monomer(s) present. Hence, homopolymers and copolymers having the same reduced viscosity or K-value can have different molecular masses. 1.3 The values determined for reduced viscosity and K-value, for a particular sample of PVC resin, are influenced differently by the concentration of the solution chosen for the determination. Hence the use of the procedures specified in this document only gives values for reduced viscosity and K-value that are comparable when the concentrations of the solutions used are identical. 1.4 The experimental procedures specified in this document can also be used to characterize the polymeric fraction obtained during the chemical analysis of a PVC composition. However, the values calculated for the reduced viscosity and K-value in these circumstances can deviate form the correct values for the resin used to produce the composition because of the impure nature of the recovered polymer fraction.

prEN 14972-18 Public enquiry
Comment end date 2026-08-25
Fixed firefighting systems - Water mist systems - Part 18: Test protocol for local application involving flammable liquid fires for open nozzle systems

This document specifies the evaluation of the fire performance of water mist systems used for local application involving flammable liquid fires. The tests specified in this document are applicable to the following: a) flammable liquid pool fires where the liquid release can be confined to a bunded area, where the entire surface of the bunded area is protected by the water mist system; b) flammable liquid channel fires in channels not exceeding the maximum specified width of the water mist system and with no limited channel length; c) partially obstructed flammable liquid pool fires where the percentage of obstructed surface is limited to that tested; d) spray fires up to 6 MW fuelled by flammable liquids; e) spray and pool fire combinations where confined to a bunded area; f) flammable liquid residues (ink and paper dust) on printing presses.

prEN IEC 61788-29:2026 Public enquiry
Comment end date 2026-09-16
Electromechanical properties measurement - Electromechanical test of practical rebco and bscco composite superconductors at liquid nitrogen temperature
prEN IEC 60335-2-38:2026 Public enquiry
Comment end date 2026-08-05
Household and similar electrical appliances - Safety - Part 2-38: Particular requirements for commercial electric griddles and griddle grills

This standard deals with the safety of electrically operated commercial griddles and griddle grills, their rated voltage being not more than 250 V for single-phase appliances connected between one phase and neutral and 480 V for other appliances

prEN 304 623 V0.1.3 (2026-06) Public enquiry
Comment end date 2026-08-31
Cyber Security (CYBER); CRA; Cybersecurity requirements for boot managers
prEN 3645-002 Public enquiry
Comment end date 2026-09-01
Aerospace series - Connectors, electrical, circular, scoop-proof, triple start threaded coupling, operating temperature 175 °C or 200 °C continuous - Part 002: Specification of performance and contact arrangements

This document specifies the performances and contact arrangements for threaded ring coupling circular connectors, fire resistant or non-fire resistant, intended for use in a temperature range from −65 °C to 175 °C or 200 °C continuous.

prEN ISO 13366-1 Public enquiry
Comment end date 2026-08-25
Milk - Enumeration of somatic cells - Part 1: Microscopic method (Reference method) (ISO/DIS 13366-1:2026)

This document specifies a microscopic method (reference method) for the counting of somatic cells in both raw and chemically preserved milk. This document is applicable for the counting of somatic cells in cows' milk, provided that the eventually mentioned prerequisites are met. This method is suitable for preparing standard test samples and determining reference method values that are required for calibrating mechanized and automated cell-counting methods.

prEN ISO 21813 Public enquiry
Comment end date 2026-09-24
Fine ceramics (advanced ceramics, advanced technical ceramics) - Methods for chemical analysis of high purity barium titanate powders (ISO/DIS 21813:2026)

ISO 21813 specifies methods for the chemical analysis of fine high purity barium titanate powders used as the raw material for fine ceramics. ISO 21813 stipulates the determination methods of the barium, titanium, aluminium, cadmium, calcium, cobalt, dysprosium, iron, lead, magnesium, manganese, nickel, niobium, potassium, silicon, sodium, strontium, vanadium, zirconium, carbon, oxygen and nitrogen contents in high purity barium titanate powders. The barium and titanium contents, the major elements, are determined by using an acid decomposition-gravimetric method or an acid decomposition-inductively coupled plasma-optical emission spectrometry (ICP-OES) method. The aluminium, cadmium, calcium, chromium, cobalt, dysprosium, iron, lead, magnesium, manganese, nickel, niobium, potassium, silicon, strontium, vanadium and zirconium contents are simultaneously determined via an acid digestion-ICP-OES method. The nitrogen content is determined by using an inert gas fusion-thermal conductivity method, while that of oxygen is determined via an inert gas fusion-IR absorption spectrometry method. Finally, the carbon content is determined using a combustion-IR absorption spectrometry method or a combustion-conductometry method.

ISO/DIS 5565-1.2 New
Comment end date 2026-08-04
Vanilla (Vanilla planifolia Andrews, syn. Vanilla fragrans Ames, and Vanilla x tahitensis JW Moore) — Part 1: Specification
prEN ISO 7198 Archived
Comment end date 2026-07-30
Cardiovascular implants and extracorporeal systems - Vascular prostheses - Tubular vascular grafts and vascular patches (ISO/DIS 7198:2026)

ISO 7198:2016 specifies requirements for the evaluation of vascular prostheses and requirements with respect to nomenclature, design attributes and information supplied by the manufacturer, based upon current medical knowledge. Guidance for the development of in vitro test methods is included in an informative annex to ISO 7198:2016. It can be considered as a supplement to ISO 14630:2012, which specifies general requirements for the performance of non-active surgical implants. NOTE Due to the variations in the design of implants covered by ISO 7198 :2016 and, in some cases, due to the relatively recent development of some of these implants (e.g. bioabsorbable vascular prostheses, cell based tissue engineered vascular prostheses), acceptable standardized in vitro tests and clinical results are not always available. As further scientific and clinical data become available, appropriate revision of ISO 7198 :2016 will be necessary. It is applicable to sterile tubular vascular grafts implanted by direct visualization surgical techniques as opposed to fluoroscopic or other non-direct imaging (e.g. computerized tomography or magnetic resonance imaging), intended to replace, bypass, or form shunts between segments of the vascular system in humans and vascular patches intended for repair and reconstruction of the vascular system. Vascular prostheses that are made of synthetic textile materials and synthetic non-textile materials are within the scope of ISO 7198:2016. While vascular prostheses that are made wholly or partly of materials of non-viable biological origin, including tissue engineered vascular prostheses are within the scope, ISO 7198:2016 does not address sourcing, harvesting, manufacturing and all testing requirements for biological materials. It is further noted that different regulatory requirements might exist for tissues from human and animal sources. Compound, coated, composite, and externally reinforced vascular prostheses are within the scope of ISO 7198:2016. Endovascular prostheses implanted using catheter delivery and non-direct visualization are excluded from the scope of ISO 7198:2016. It includes information on the development of appropriate test methods for graft materials, referenced in ISO 25539‑1 for materials used in the construction of endovascular prostheses (i.e. stent-grafts). NOTE Requirements for endovascular prostheses are specified in ISO 25539‑1. The valve component of valved conduits constructed with a tubular vascular graft component, and the combination of the valved component and the tubular vascular graft component, are excluded from the scope of ISO 7198:2016. It can be helpful in identifying the appropriate evaluation of the tubular vascular graft component of a valved conduit but specific requirements and testing are not described for these devices. Cardiac and pericardial patches, vascular stents, accessory devices such as anastomotic devices, staplers, tunnelers and sutures, and pledgets are excluded from the scope of ISO 7198:2016. NOTE Requirements for vascular stents are specified in ISO 25539‑2. Requirements regarding cell seeding are excluded from the scope of ISO 7198:2016. Tissue engineered vascular prostheses that contain or are manufactured using cells present many distinct manufacturing (e.g. aseptic processing, cell seeding, etc.) and testing issues than those produced with synthetic or non-viable biological materials. The in vitro testing requirements that are outlined in ISO 7198:201

prEN ISO 81060-2 Public enquiry
Comment end date 2026-08-27
Non-invasive sphygmomanometers - Part 2: Clinical performance verification of intermittent automated measurement type (ISO/DIS 81060-2:2026)

This document specifies the requirements and methods for the clinical investigation of me equipment used for the intermittent non-invasive automated estimation of the arterial blood pressure by utilizing a cuff. This document is applicable to all sphygmomanometers that sense or display pulsations, flow or sounds for the estimation, display or recording of blood pressure. These sphygmomanometers need not have automatic cuff inflation. This document covers sphygmomanometers intended for use in all patient populations (e.g. all age and weight ranges), and all conditions of use (e.g. ambulatory blood pressure monitoring, stress testing blood pressure monitoring and blood pressure monitors for the home healthcare environment for self-measurement as well as use in a professional healthcare facility). EXAMPLE Automated sphygmomanometer as given in IEC 80601-2-30 undergoing clinical investigation according to this document. This document specifies additional disclosure requirements for the accompanying documents of sphygmomanometers that have passed a clinical investigation according to this document. This document is not applicable to clinical investigations of non-automated sphygmomanometers as given in ISO 81060-1 or invasive blood pressure monitoring equipment as given in IEC 60601-2-34. This document is not applicable to clinical investigations of a set of cuffs that are not of same materials and construction. Each type of cuff set is required to be evaluated separately according to this document.

prEN 50174-3:2026 Public enquiry
Comment end date 2026-09-04
Information technology - Cabling installation - Part 3: Installation planning and practices outside buildings

This document specifies requirements and provides recommendations for the following aspects of information technology cabling: a) planning; b) installation practice. This document is applicable to all types of information technology cabling outside buildings including generic cabling systems designed in accordance with EN 50173 series. The requirements and recommendations of this document can be applied to cabling that is defined as part of the building. The requirements and recommendations of Clauses 5, 6 and 7 of this document are subject to any site-specific requirements and recommendations of Clause 8. The planning of the pathway systems, spaces and structures within the core and access network cabling as described in Figure 2 that are owned by access providers is excluded except for requirements and recommendations that provide basic safety, function and environmental objectives for mechanical, ingress and climatic characteristics (i.e. excluding pathway dimensions, distribution of spaces and similar constraints based on specific transmission methods). The installation practices applicable to all cabling installation methods are included by the provision of the necessary planning requirements and recommendations associated with each one with the exception of information technology cabling installed: – around or within aerial power supply or associated earth conductors; – on infrastructures carrying power supplies in excess of AC/DC 25 kV. This document: 1) details the considerations for satisfactory installation and operation of information technology cabling; 2) excludes specific requirements applicable to other cabling systems (e.g. power supply cabling); however, it takes account of the effects other cabling systems may have on the installation of information technology cabling (and vice versa) and gives general advice; 3) excludes those aspects of installation associated with the transmission of signals in free space between transmitters, receivers or their associated antenna systems (e.g. wireless, radio, microwave or satellite). This document is applicable to certain hazardous environments. It does not exclude additional requirements which are applicable in particular circumstances, defined by e.g. electricity supply and electrified railways. The requirements within this document cover any additional requirements for the information technology cables installed in hazardous or stressful environments e.g. electricity supply and electric railway locations (see Clause 8). Safety (electrical safety and protection, optical power, fire protection, etc.) and electromagnetic compatibility (EMC) requirements are outside the scope of this document and are covered by other standards and regulations. However, information given in this document can be of assistance in meeting these standards and regulations. Examples of areas covered by this document are shown in Figure 2.

ISO/DIS 6575 Public enquiry
Comment end date 2026-09-19
Fenugreek, whole or ground (powdered) — Specification
Total records found: 262
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