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Total records found: 286
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prEN ISO 22523 Public enquiry
Comment end date 2026-05-05
External limb prostheses and external orthoses - Requirements and test methods (ISO/DIS 22523:2026)

This document specifies requirements and test methods for external limb prostheses and external orthoses, including the following classifications from ISO 9999: 06 03 - 06 15 Orthoses 06 18 - 06 27 Limb prostheses It covers strength, materials, restrictions on use, risk and the provision of information associated with the normal conditions of use of both components and assemblies of components. This document is also applicable as a guide in the design and test of custom build orthosis and prosthesis. NOTE The application of Quality Systems as described or referred to in ISO 13485 and ISO 13488 can be appropriate.

ISO/DIS 18981 Public enquiry
Comment end date 2026-03-30
Tourism and related services — Restaurants – Guidelines for buffet design and services
prEN ISO 3826-2 Public enquiry
Comment end date 2026-04-16
Plastics collapsible containers for human blood and blood components - Part 2: Graphical symbols for use on labels and instruction leaflets (ISO/DIS 3826‑2:2026)

This document addresses symbols that may be used to convey certain items of information related to medical devices dedicated to blood collection processes and storage. The information may be required on the device itself, as part of the label, or provided with the device. Many countries require that their own language be used to display textual information with medical devices. This raises problems to device manufacturers and users. The symbols specified in this document do not replace current national regulatory requirements. Manufacturers seek to take costs out of labelling by reducing or rationalizing variants. This results in a major problem of translation, design and logistics when multiple languages are included on a single label or piece of documentation.  As other medical devices, blood medical devices, labelled in a number of different languages, can experience confusion and delay in locating the appropriate language. This document proposes solutions to these problems through the use of internationally recognized symbols with precisely defined meanings. This document is primarily intended to be used by manufacturers of medical devices dedicated to the blood collection, process storage and distribution, who market identical products in countries having different language requirements for medical device labelling. This document may also be of assistance to different stages of the blood supply chain, e.g.: distributors of blood collection devices (manual or automated) or other representatives of manufacturers; blood centres and distribution centres to simplify and secure the operating procedures. The use of these symbols is primarily intended for the medical device rather than the therapeutic product. This document does not specify requirements relating to the size and colour of symbols although the symbols specified have been specially designed so as to be clearly legible when reproduced in the space typically available on the labels of blood treatment and transfusion devices, and also so as to be suitable for on-line printing. Several of the symbols specified in this document may be suitable for application in other areas of medical technology.

prEN ISO 7817-3 Public enquiry
Comment end date 2026-04-21
Building information modelling - Level of information need - Part 3: Data model and schema (ISO/DIS 7817-3:2026)

The standard specifies a data model in UML and a derived XML schema (XSD) for defining the Level of Information Need in software applications based on concepts and principles given in Part 1, and guidance given in Part 2, in compliance with the principles and data exchange standards of data templates (ISO 23387). The standard defines the exchange format schema in XSD according to the UML schema and it gives guidelines for the usage and application of the schema. In addition, the integration with Linked Data principles and paradigms will be demonstrated.

prEN ISO 27789 Public enquiry
Comment end date 2026-05-14
Health informatics - Audit trails for electronic health records (ISO/DIS 27789:2026)

This document specifies a common framework for audit trails for electronic health records (EHR), in terms of audit trigger events and audit data, to keep the complete set of personal health information auditable across information systems and domains. It is applicable to systems processing personal health information that create a secure audit record each time a user reads, creates, updates, or archives personal health information via the system. NOTE       Such audit records at a minimum uniquely identify the user, uniquely identify the subject of care, identify the function performed by the user (record creation, read, update, etc.), and record the date and time at which the function was performed. This document covers only actions performed on the EHR, which are governed by the access policy for the domain where the electronic health record resides. It does not deal with any personal health information from the electronic health record, other than identifiers, the audit record only containing links to EHR segments as defined by the governing access policy. It does not cover the specification and use of audit logs for system management and system security purposes, such as the detection of performance problems, application flaw, or support for a reconstruction of data, which are dealt with by general computer security standards such as ISO/IEC 15408 (all parts)[9]. Annex A gives examples of audit scenarios. Annex B gives an overview of audit log services.

prEN IEC 62822-2:2026 Public enquiry
Comment end date 2026-05-15
Electric welding equipment - Assessment of restrictions related to human exposure to electromagnetic fields (0 Hz to 300 GHz) - Part 2: Arc welding equipment
prEN IEC 63418:2026 Public enquiry
Comment end date 2026-05-20
Fixed accessories intended for household and similar purposes that supply power through an interface
prEN 13075-2 Archived
Comment end date 2026-03-27
Bitumens and bituminous binders - Determination of breaking behaviour - Part 2: Determination of fines mixing time of cationic bituminous emulsions

This document specifies a method for the determination of the fines mixing time of diluted cationic bituminous emulsions, under standardized conditions. WARNING - Use of this document can involve hazardous materials, operations and equipment. This document does not purport to address all of the safety problems associated with its use. It is the responsibility of the user of this document to identify the hazards and assess the risks involved in performing this test method and to implement sufficient control measures to protect individual operators (and the environment). This includes appropriate safety and health practices and determination of the applicability of regulatory limitations prior to use.

EN 50110-1:2023/prA1:2026 Public enquiry
Comment end date 2026-04-22
Operation of electrical installations - Part 1: General requirements

This standard is applicable to all operation of and work activity on, with, or near electrical installations. These are electrical installations operating at voltage levels from and including extra-low voltage up to and including high voltage. This latter term includes those levels commonly referred to as medium and extra-high voltage

prEN IEC 61850-7-400:2026 Public enquiry
Comment end date 2026-04-22
Communication networks and systems for power utility automation - Part 7-400: Basic communication structure - Compatible logical node classes and data object classes - Substation automation
prEN IEC 60071-14:2026 Public enquiry
Comment end date 2026-05-13
Insulation co-ordination - Part 14: Application procedures for AC/DC filters
prEN 149 Public enquiry
Comment end date 2026-05-21
Respiratory protective devices - Filtering half masks to protect against particles - Requirements, testing and marking

This document specifies minimum requirements for particle filtering half masks as respiratory protective devices intended to protect the wearer in occupational settings, where there is a health risk(s) from inhaling any type of particles during working activities except for escape purposes. Laboratory and practical performance tests or references to test method standards are included for the assessment of compliance with the requirements.

prEN 301 406-1 V3.2.0 (2026-01) Archived
Comment end date 2026-03-22
Digital Enhanced Cordless Telecommunications (DECT); Harmonised Standard for access to radio spectrum; Part 1: DECT, DECT Evolution and DECT ULE
prEN 301 545-2 V1.5.1 (2026-01) Public enquiry
Comment end date 2026-04-12
Digital Video Broadcasting (DVB); Second Generation DVB Interactive Satellite System (DVB-RCS2); Part 2: Lower Layers for Satellite standard
prEN IEC 63533:2026 Public enquiry
Comment end date 2026-04-15
Germicidal equipment - Airborne microorganisms inactivation by Germicidal Ultraviolet (GUV) luminaires
prEN IEC 61850-7-4:2026 Public enquiry
Comment end date 2026-04-22
Communication networks and systems for power utility automation - Part 7-4: Basic communication structure - Compatible logical node classes and data object classes
ISO/DIS 13228 Public enquiry
Comment end date 2026-05-18
Road vehicles — Test method for automotive LiDAR
prEN IEC 61202-1:2026 Public enquiry
Comment end date 2026-05-15
Fibre optic interconnecting devices and passive components - Fibre optic isolators - Part 1: Generic specification
prEN ISO 13760 Archived
Comment end date 2026-03-24
Plastics pipes for the conveyance of fluids under pressure - Miner's rule - Calculation method for cumulative damage (ISO/DIS 13760:2026)

In general terms, Miner’s rule is a common approach to calculate how the accumulation of a specific load that varies over time effects the time until failure. This international standard specifies the application of Miner’s rule for calculating the design time until failure of plastics pipes and piping systems of plastics materials under varying, but known, load conditions. Miner’s rule can also be applied reciprocally to calculate the tolerable load levels along a desired design time. This international standard specifies particularly the application of Miner’s rule to calculate stress or pressure regimes, respectively, that are tolerable during a targeted design time for plastics or composite pipes. Further, the application of Miner’s rule on the effect of accumulated damage on polyolefins caused by oxidative attack under varying temperatures and times on the design life is specified. It is necessary to apply Miner's rule to each failure mechanism separately. Thus, for mechanical failure due to internal pressure, other failure mechanisms, such as oxidative or dehydrochlorinative degradative failure mechanisms, are to be neglected (assuming, of course, no interaction). A material may be used only when it is proven to conform to all failure mechanism criteria. NOTE Miner's rule is an empirically based procedure and is only a first approximation to reality.

prEN IEC 61951-1:2026 Public enquiry
Comment end date 2026-04-03
Secondary cells and batteries containing alkaline or other non-acid electrolytes - Secondary sealed cells and batteries for portable applications - Part 1: Nickel-Cadmium
ISO/IEC 29192-8:2022/DAmd 1 Public enquiry
Comment end date 2026-04-12
Information security — Lightweight cryptography — Part 8: Authenticated encryption — Amendment 1
prEN ISO 25935 Public enquiry
Comment end date 2026-04-21
Geometrical product specifications (GPS) - Restrained states (ISO/DIS 25935:2026)

This document specifies rules for restrained states.

EN 1396:2023/prA1 Public enquiry
Comment end date 2026-05-24
Aluminium and aluminium alloys - Coil coated sheet and strip for general applications - Specifications

This document specifies the particular requirements for wrought aluminium and wrought aluminium alloys in the form of coil coated sheet and strip for general applications. This product is generally supplied in thicknesses up to 3,0 mm. It is applicable to cold-rolled aluminium and aluminium alloy strip coated by the coil coating process both with liquid as well as with powder paints, either in the final width or slit afterwards, and to sheet obtained from such strip. It does not apply to coil coated sheet and strip used for special applications such as cans, closures and lids which are dealt with in separate EN 541.

prEN IEC 61010-2-034:2026 Public enquiry
Comment end date 2026-05-20
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-034: Particular requirements for measurement equipment for insulation resistance and test equipment for electric strength
prEN ISO 18730 Archived
Comment end date 2026-03-24
Anaesthetic and respiratory equipment - Waste volatile anaesthetic agent capture systems (ISO/DIS 18730:2026)

This document specifies requirements for waste volatile anaesthetic agent capture systems that may or may not include the recycling of the collected volatile anaesthetic agent for reuse. NOTE 1: Waste volatile agent capture systems, that are part of a medical gas pipeline system as specified in ISO 7396-1 [4], are outside the scope of this document. NOTE 2: Nitrous oxide is not considered to be a volatile anaesthetic agent.

Total records found: 286
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