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Total records found: 250
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prEN 17461 Public enquiry
Comment end date 2026-07-07
Gymnastic equipment - Individual and multifunctional vaulting boxes - Safety requirements and test methods

This document specifies functional requirements and specific safety requirements in addition to the general safety standard EN 913 for gymnastic and vaulting boxes for individual or multifunctional use. This document also specifies requirements when multifunctional boxes are used in combination with accessories.

ISO/DIS 23640 Public enquiry
Comment end date 2026-07-13
In vitro diagnostic medical devices — Evaluation of stability of in vitro diagnostic reagents
prEN ISO 7198 Public enquiry
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

EN 1997-1:2024/prA1 Public enquiry
Comment end date 2026-08-13
Eurocode 7 - Geotechnical design - Part 1: General rules

1.1 Scope of EN 1997 1 (1) This document provides general rules for the design and verification of geotechnical structures. (2) This document is applicable for the design and verification of geotechnical structures outside the scope of EN 1997 3. NOTE In this case, additional or amended provisions can be necessary. 1.2 Assumptions (1) In addition to the assumptions given in EN 1990, the provisions of EN 1997 (all parts) assume that: — ground investigations are planned by individuals or organisations with knowledge of potential ground and groundwater conditions; — ground investigations are executed by individuals with appropriate skills and experience; — the evaluation of test results and derivation of ground properties from the ground investigation are carried out by individuals with appropriate geotechnical experience and qualifications; — the data required for design are collected, recorded, and interpreted by appropriately qualified and experienced individuals; — geotechnical structures are designed and verified by individuals with appropriate qualifications and experience in geotechnical design; — adequate continuity and communication exist between the individuals involved in data collection, design, verification and execution. (2) This document is intended to be used in conjunction with EN 1990, which establishes principles and requirements for the safety, serviceability, robustness, and durability of structures, including geotechnical structures, and other construction works. NOTE Additional or amended provisions can be necessary for assessment of existing structures, see EN 1990 2. (3) This document is intended to be used in conjunction with EN 1997 2, which gives provisions for determining ground properties from ground investigations. (4) This document is intended to be used in conjunction with EN 1997 3, which gives specific rules for the design and verification of certain types of geotechnical structures. (5) This document is intended to be used in conjunction with other Eurocodes for the design of geotechnical structures, including temporary geotechnical structures.

EN 61754-4-100:2016/prA1:2026 Public enquiry
Comment end date 2026-08-28
Amendment 1 - Fibre optic interconnecting devices and passive components - Fibre optic connector interfaces - Part 4-100: Type SC connector family - Simplified receptacle SC-PC connector interfaces
prEN IEC 63409-7:2026 Public enquiry
Comment end date 2026-07-08
Photovoltaic power generating systems connection with the grid - Testing of power conversion equipment - Part 7: Remote configuration, control and monitoring
EN IEC 62083:2026/prA1:2026 Public enquiry
Comment end date 2026-07-22
Amendment 1 - Medical device software - Requirements for the safety of radiotherapy treatment planning systems
prEN ISO/IEC 19788-3 Public enquiry
Comment end date 2026-07-28
Information technology for learning, education and training - Metadata for learning resources - Part 3: Basic application profile (ISO/DIS 19788-3:2026)

The primary purpose of ISO/IEC 19788 is to specify metadata elements and their attributes for the description of learning resources. This includes the rules governing the identification of data elements and the specification of their attributes. ISO/IEC 19788 provides data elements for the description of learning resources and resources directly related to learning resources. ISO/IEC 19788-3:2011 is designed to help implementers with a starting point for adopting ISO/IEC 19788, defining an application profile that specifies, through adding constraints to the use of some data elements, how the ISO/IEC 19788-2 element set can be used.

prEN IEC 62052-11:2026 Public enquiry
Comment end date 2026-08-12
Electricity metering equipment - General requirements, tests and test conditions - Part 11: Metering equipment
prEN IEC/IEEE 62704-4:2026 Public enquiry
Comment end date 2026-08-19
Determining the peak spatial-average specific absorption rate (SAR) in the human body from wireless communication devices, 100 kHz to 10 GHz - Part 4: General requirements for using the finite element method for SAR calculations
prEN 9300-021 Public enquiry
Comment end date 2026-09-01
Aerospace series - LOTAR - LOng Term Archiving and Retrieval of digital technical product documentation such as 3D, CAD and PDM data - Part 021: Metadata for archival packages

This document specifies requirements for metadata of archive packages intended for the long-term archiving of digital product information.

ISO/DIS 11452-8.2 Public enquiry
Comment end date 2026-08-15
Road vehicles — Component test methods for electrical disturbances from narrowband radiated electromagnetic energy — Part 8: Immunity to magnetic fields
prEN 15430-3 Public enquiry
Comment end date 2026-07-05
Winter and road service area maintenance equipment - Data acquisition and transmission - Part 3: Protocol for data transfer between application servers

The function of EN 15430 is to combine any vehicle equipment with different board computers to any client application server. This document specifies the interface and protocol needed between the information supplier server and the client application server (flow 3 as illustrated in Figure 1) to allow distribution of data without any restrictions to the technology used to gather the data like manufacturer specific protocols, WLANS systems, memory cards, etc.

prEN 13209-2 Public enquiry
Comment end date 2026-07-21
Child care articles - Baby carriers - Safety requirements and test methods - Part 2: Soft carrier

This document specifies the safety requirements and test methods for soft carriers without a framed support designed to carry one or two children hands free when attached to the carer’s torso. If the soft carrier has functions not covered in this document, reference can be made to the relevant European Standard. This document does not apply to garment or apparel carriers or carriers in the scope of prEN 13209 3:2026. This document does not cover baby carriers designed for children with special needs.

prEN ISO 1924-2 Public enquiry
Comment end date 2026-07-30
Paper and board - Determination of tensile properties - Part 2: Constant rate of elongation method (20 mm/min) (ISO/DIS 1924-2:2026)

ISO 1924-2:2008 specifies a method for measuring the tensile strength, strain at break and tensile energy absorption of paper and board, using a testing machine operating at a constant rate of elongation (20 mm/min). ISO 1924-2:2008 also specifies equations for calculating the tensile index, the tensile energy absorption index and the modulus of elasticity. Testing in conformance with ISO 1924-2:2008 always includes the measurement of tensile strength. Measurement or calculation of other properties is subject to agreement between the parties concerned. ISO 1924-2:2008 is applicable to all papers and boards, including papers with a high strain at break if the results are within the capacity of the testing machine. It also applies to the components of corrugated board but not, however, to corrugated board itself.

prEN ISO 16371-1 Public enquiry
Comment end date 2026-08-20
Non-destructive testing — Industrial computed radiography with storage phosphor imaging plates — Part 1: Classification of systems

This document specifies fundamental parameters of computed radiography (CR) systems with the aim of enabling satisfactory and repeatable results to be obtained economically. The techniques are based both on fundamental theory and test measurements. This document specifies the performance of CR systems and the measurement of the corresponding parameters for the system scanner and storage phosphor imaging plate (IP). CR system classes are defined in combination with specified metal screens for industrial radiography. This document ensures that the quality of the images, as far as they are influenced by the scanner IP system, complies with the requirements of ISO 16371-2. This document considers the requirements for film radiography specified in ISO 11699-1. This document specifies system tests at different levels. More complex manufacturer tests are described, which allow the determination of precise system parameters to characterize the performance of  CR systems from different suppliers and make them comparable for users. Simpler tests are also described, which are designed for fast tests of the quality of CR systems and long-term stability monitoring by the user.

EN IEC 60721-3-4:2019/prA1:2026 Public enquiry
Comment end date 2026-08-21
Amendment 1 - Classification of environmental conditions - Part 3-4: Classification of groups of environmental parameters and their severities - Stationary use at non-weatherprotected loca-tions
prEN ISO 11138-6 Public enquiry
Comment end date 2026-07-21
Sterilization of health care products - Biological indicators - Part 6: Biological indicators for vaporized hydrogen peroxide sterilization processes (ISO/DIS 11138-6:2026)

This document specifies requirements for test organisms, inoculated carriers, biological indicators and test methods intended for use in assessing the performance of sterilizers and sterilization processes employing vaporized hydrogen peroxide as the sterilizing agent. NOTE 1 Requirements for validation and control of vaporized hydrogen peroxide sterilization processes are provided by ISO 22441 and ISO 14937. NOTE 2 National or regional regulations can provide requirements for workplace safety.

ISO/DIS 25608 Public enquiry
Comment end date 2026-07-25
Healthcare organization management — Smart hospitals — RTLS for portable devices
EN 17339:2024/prA1 Public enquiry
Comment end date 2026-08-06
Transportable gas cylinders - Hoop wrapped and fully wrapped carbon composite cylinders and tubes for hydrogen

This document specifies minimum requirements for the materials, design, construction, prototype testing and routine manufacturing inspections of composite gas cylinders and tubes for compressed hydrogen. NOTE 1 Unless specified in the text, for the purposes of this document, the word “cylinder” includes tubes. This document applies to - fully wrapped composite cylinders (Type 3 and Type 4) - hoop wrapped cylinders (Type 2) with carbon fibres intended to be permanently mounted in a frame (e.g. bundle or trailer) with a test pressure of not less than 300 bar, with: — non-metallic liners (for Type 4) or seamless metallic liners (for Type 2 and Type 3), — a maximum water capacity of 3 000 l — a maximum working pressure of 1 000 bar. — the product of working pressure times water capacity (p x V) not exceeding 1 000 000 bar.l. NOTE 2 A glass fibre protective layer is sometimes applied to the external surface of the cylinder

prEN IEC 60335-2-47:2026/prAA:2026 Public enquiry
Comment end date 2026-08-19
Household and similar electrical appliances - Safety - Part 2-47: Particular requirements for commercial electric boiling pans

This European Standard deals with the safety of electrically operated commercial boiling pans not intended for household use. The rated voltage being not more than 250 V for single-phase appliances connected between one phase and neutral, and 480 V for other appliances. Appliances which are within the scope of this standard are typically used in restaurants, canteens, hospitals and commercial enterprises such as bakeries, butcheries,etc.

prEN 50340:2026 Public enquiry
Comment end date 2026-07-22
Hydraulic cable cutting devices to be used on electrical installations with nominal voltage up to 60 kV AC

This document is applicable to cable cutting devices to be used to verify that a cable is dead in accordance with the rules given in EN 50110. NOTE It can also be used as an example when dismantling cable installations. The following limits apply to the cable cutting devices: - pressure less than 1 000 bar or pressure (bar) x volume (l) less than 10 000; - fluid outside the categories listed in Article 13 Group 1 (explosive, extremely flammable, highly flammable, flammable (where the maximum allowable temperature is above flashpoint), very toxic, toxic, oxidizing) of the Pressure Equipment Directive 2014/68/EU. Cable cutting devices specified in this document are for use on systems with nominal voltage up to 60 kV AC and nominal frequencies up to 60 Hz and are only suitable for operation by foot or by hand. This document does not cover motorised cable cutting devices. This document is intended to be used as a guide for devices to be used on systems with nominal voltages above 60 kV AC, but additional requirements and tests can be agreed between manufacturer and customer to provide an equivalent level of safety. Cable cutting devices are not designed to be used on cables with special armour, or with steel wires or steel tapes more than 1 mm in diameter or thickness. The products designed and manufactured according to this document contribute to the safety of the users provided they are used by skilled persons, in accordance with safe methods of work and the instructions for use.

prEN IEC 60335-2-39:2026 Public enquiry
Comment end date 2026-07-29
Household and similar electrical appliances - Safety - Part 2-39: Particular requirements for commercial electric multi-purpose cooking pans

This European Standard Deals with the safety of electrically operated commerical multi-purpose cooking pans not intended for household use. The rated voltage being not more than 250 V for single-phase appliances connected between one phase and neutral and 480 V for other appliances. Appliances within the scope of this standard are typically used in restaurants, canteens, hospitals, and commercial enterprises such as bakeries, butcheries, etc. The electrical part of appliances making use of other forms of energy is also within the scope of this standard.

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 ISO 13366-2 Public enquiry
Comment end date 2026-08-25
Milk - Enumeration of somatic cells - Part 2: Flow cytometry method (ISO/DIS 13366-2:2026)

ISO 13366-2|IDF 148-2:2006 gives guidance on the operating conditions for counting somatic cells, in both raw and chemically preserved milk, using fluoro-opto-electronic somatic cell counters in which either a rotating disc technique or flow cytometry is applied in the counting section. The guidance is applicable to the counting of somatic cells in raw cow milk. The guidance is also applicable to raw milk of other species, such as goat, sheep and buffalo, if the specified prerequisites are met.

Total records found: 250
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