Standartų projektų sąrašas

prEN 302 448 V2.1.18 (2026-09) Naujas

Komentavimo iki data 2026-11-28

Palydovinės Žemės stotys ir sistemos (PŽSS). Traukiniuose įrengtos Žemės stotys, veikiančios 11/12/14 GHz dažnių juostose. Prieigos prie radijo ryšio spektro darnusis standartas

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prEN ISO 3821 Viešoji apklausa

Komentavimo iki data 2026-11-26

Dujinio suvirinimo įranga. Suvirinimo, pjaustymo ir panašių procesų guminės žarnos (ISO/DIS 3821:2026)

This document specifies requirements for rubber hoses (including twin hoses) for welding, cutting and allied processes. This document specifies requirements for rubber hoses for normal duty of 2 MPa (20 bar) and light duty [limited to hoses for maximum working pressure of 1 MPa (10 bar) and with bore up to and including 6,3 mm]. This document applies to hoses operated at temperatures −20 °C to +60 °C and used in: — gas welding and cutting; — arc welding under the protection of an inert or active gas; — processes allied to welding and cutting, in particular, heating, brazing, and metallization. This document does not specify requirements for hose assemblies; these are detailed in ISO 8207. This document applies neither to thermoplastics hoses nor to hoses used for high pressure [>0,15 MPa (>1,5 bar)] acetylene.

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prEN ISO 5359 Viešoji apklausa

Komentavimo iki data 2026-11-26

Anestezijos ir kvėpavimo įranga. Mažaslėgių žarnų sąrankos, skirtos medicininėms dujoms (ISO/DIS 5359:2026)

ISO 5359:2014 specifies requirements for low-pressure hose assemblies intended for use with the following medical gases: oxygen, nitrous oxide, medical air, helium, carbon dioxide, xenon, specified mixtures of the gases listed above, oxygen-enriched air, air for driving surgical tools, nitrogen for driving surgical tools, and for use with vacuum. It applies to hose assemblies operating at pressures up to 1 400 kPa and for vacuum systems at pressures not greater than 60 kPa absolute. It does not specify the dimensions and allocation of the gas-specific inlet and outlet connectors for the hose assemblies.It does not specify requirements for coaxial hoses used for the supply and removal of air for driving surgical tools.Nor does it specify the intended uses of hose assemblies.

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prEN ISO 18082 Viešoji apklausa

Komentavimo iki data 2026-11-26

Anaesthetic and respiratory equipment - Dimensions of non-interchangeable screw-threaded (NIST) low-pressure connectors for medical gases (ISO/DIS 18082:2026)

ISO 18082:2014 specifies the dimensions, the allocation and marking of non-interchangeable screw-threaded (NIST) connectors intended to be used at operating pressures up to 1 400 kPa, and for vacuum systems at pressures not greater than 60 kPa absolute. ISO 18082:2014 specifies NIST connectors intended for use with the following medical gases: oxygen; nitrous oxide; medical air; helium; carbon dioxide; xenon; specified mixtures of the gases listed above; oxygen-enriched air; air for driving surgical tools; nitrogen for driving surgical tools; use with vacuum.

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prEN ISO 15883-4 Viešoji apklausa

Komentavimo iki data 2026-11-26

Dezinfekavimo plautuvai. 4 dalis. Dezinfekavimo plautuvų, skirtų termolabiliesiems endoskopams chemiškai dezinfekuoti, reikalavimai ir bandymai (ISO/DIS 15883-4:2026)

This document specifies the particular requirements, including performance criteria for washer-disinfectors (WD) that are intended to be used for cleaning and chemical disinfection of thermolabile endoscopes. This document also specifies the performance requirements for the cleaning and disinfection of the washer-disinfector and its components and accessories which can be required to achieve the necessary performance criteria. The methods, instrumentation and instructions required for type testing, works testing, validation (installation, operational and performance qualification on first installation), routine control and monitoring, and requalification of WD periodically and after essential repairs, are also specified. NOTE 1 In addition, Annex A gives guidance on an appropriate division of responsibility for the range of activities covered by this document. NOTE 2 WD complying with this document can also be used for cleaning and chemical disinfection of other thermolabile re-usable medical devices for which the device manufacturer has recommended and validated this method of disinfection. WD complying with the requirements of this document are not intended for cleaning and disinfection of medical devices, including endoscopic accessories, which are heat stable and can be disinfected or sterilized by thermal methods (see ISO 15883-1:2006+Amd 1:2014, 4.1.5). The specified performance requirements of this document do not ensure the inactivation or removal of the causative agent(s) (prion protein) of transmissible spongiform encephalopathies. NOTE 3 If it is considered that prion protein might be present, particular care is needed in the choice of cleaning agents and disinfectants to ensure that the chemicals used do not react with the prion protein and/or other protein in a manner that can inhibit its removal or inactivation from the load or washer-disinfector. NOTE 4 This document can be used by prospective purchasers and manufacturers as the basis of agreement on the specification of the WD, manufacturers of endoscopes, cleaning products, and disinfecting products.

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prEN ISO 5667-3 Viešoji apklausa

Komentavimo iki data 2026-11-24

Vandens kokybė. Mėginių ėmimas. 3 dalis. Vandens mėginių konservavimas ir tvarkymas (ISO/DIS 5667-3:2026)

This document specifies the general requirements for sampling, preservation, handling, transport and storage of all water samples for physicochemical, chemical, hydrobiological and microbiological analyses and determination of radiochemical analytes and activities. Guidance on the validation of storage times of water samples is provided in ISO/TS 5667-25 [2]. This document is not applicable to water samples intended for ecotoxicological assays, biological assays (which is specified in ISO 5667-16 [4]), passive sampling (which is specified in ISO 5667-23 [5]) and microplastics (which is specified in ISO 5667-27 [6]). This document is particularly appropriate when samples cannot be analysed on site and have to be transported to a laboratory for analysis.

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prEN IEC 63758-5-1:2026 Viešoji apklausa