Toimialayhteisöt

 

Tämä standardi kattaa vaatimukset ja ohjeet uudelleenkäytettävien ontelolaattojen tarkastamiselle, irrottamiselle, kunnostukselle, testaukselle, suunnittelulle ja dokumentoinnille uudelleenkäyttöä varten. Uudelleenkäytettyjä ontelolaattoja käytetään vastaavissa rakenteissa ja käyttökohteissa kuin standardin SFS-EN 1168:2005 + A3:2012 mukaisia uusia ontelolaattoja. Tämän standardin piiriin kuuluvat ekstruuderi- tai liukuvalutekniikalla kertavalulla valmistetut enintään 1200 mm levyiset tai siitä sahaamalla kavennetut ontelolaatat. Standardin piiristä rajataan pois kololaatat. Tämä asiakirja ei määrittele projektikohtaisia yksityiskohtaisia suunnitteluvaatimuksia. Uudelleenkäytettävien ontelolaattojen suunnittelu toteutetaan eurokoodin SFS-EN 1992-1-1:2005 + A1:2015 + AC:2010 ja sen kansallisen liitteen mukaan. Tässä standardissa esitetään, miten saavutetaan eurokoodissa tarvittavat laskentaparametrit ja standardissa SFS-EN 1168:2005 + A3:2012 esitetyt ontelolaattojen oleelliset vaatimukset.

 

Tämä standardi sisältää nestekaasun ja maakaasun käyttölaitteiden ja niihin liitettyjen putkistojen kaavioissa ja piirustuksissa käytettäviksi soveltuvat piirrosmerkit.

 

Standardi esitetään kumottavaksi vanhentuneena  

SFS:n tehtävänä on ylläpitää ajantasaista suomalaista SFS-standardikokoelmaa. 

Tällä lausuntopyynnöllä pyritään selvittämään, tulisiko tämä SFS-standardi kumota vanhentuneena. 

Vastaa kohdassa "Ota kantaa", tulisiko tämä SFS-standardi kumota.  

(Hyväksyn = hyväksyn tämän standardin kumoamisen vanhentuneena.)

 

This document specifies the general requirements for unmanned aircraft docking systems, including the requirements for basic characteristics, functional capabilities, performance criteria, environmental adaptability, electromagnetic compatibility, safety, reliability, maintainability, and testability, as well as the guidelines for marking and packaging. This document applies to the docking systems of civil small multi-copter unmanned aircraft with a maximum take-off mass (MTOM) of level II through level IV as defined in ISO 21895. Docking system supporting other types of unmanned aircraft may also refer to this document. This document does not specify the requirements for vertiports, which are operated under the responsibility of vertiport operators as defined in ISO 5015-2.

 

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 WD 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 conforming 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 conforming 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 15883-1:2024, 4.1.5). NOTE 3 The specified performance requirements of this document cannot ensure the inactivation or removal of the causative agent(s) (prion protein) of transmissible spongiform encephalopathies. NOTE 4 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 or other protein in a manner that can inhibit its removal or inactivation from the load or WD. NOTE 5 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.

 

This document defines several subsets of the syntax specified in ISO/IEC 21122-1 as profiles. It also defines lower bounds on the throughput in the decoded domain via levels and the encoded domain via sublevels that a conforming decoder implementation shall support. Furthermore, it defines a buffer model to ensure interoperability between implementations in the presence of a latency constraint.

 

This specification defines the Trusted Platform Module (TPM) a device that enables trust in computing platforms in general. It is broken into parts to make the role of each part clear. All parts are required in order to constitute a complete standard.

 

For a complete definition of all requirements necessary to build a TPM, the designer will need to use the appropriate platform-specific specification to understand all of the requirements for a TPM in a specific application or make appropriate choices as an implementer.

 

Those wishing to create a TPM need to be aware that this specification does not provide a complete picture of the options and commands necessary to implement a TPM. To implement a TPM the designer needs to refer to the relevant platform-specific specification to understand the options and settings required for a TPM in a specific type of platform or make appropriate choices as an implementer.

 

The number of platform configuration registers and their attributes are not defined in this specification. Those values would be specified by a platform specific specification or alternatively determined by an implementer. 

 

This part of the Trusted Platform Module Library specification contains the definitions of the constants, flags, structure, and union definitions used to communicate with the TPM. Values defined in this document are used by the TPM commands defined in ISO/IEC 11889 Part 3: Commands and by the functions in the Reference Code.

 

NOTE The structures in this document are the canonical form of the structures on the interface. All structures are “packed” with no octets of padding between structure elements. The TPM-internal form of the structures is dependent on the processor and compiler for the TPM implementation.

 

This ISO/IEC 11889 Part 3 of the Trusted Platform Module Library specification contains the definitions of the TPM commands. These commands make use of the constants, flags, structures, and union definitions defined in ISO/IEC 11889 Part 2.

 

The combination of this ISO/IEC 11889 Part 3 and the Reference Code is sufficient to fully describe the required behavior of a TPM. The Reference Code is written to define the behavior of a compliant TPM. In some cases (e.g., firmware update), it is not practical to require a single compliant implementation. In those cases, any implementation provided by the vendor that meets the general description of the function provided in ISO/IEC 11889 Part 3 would be compliant.

 

The Reference Code is not written to meet any particular level of conformance nor does this specification require that a TPM meet any particular level of conformance.

 

This document defines terms and expressions used in the field of underwater bioacoustics and biotremology, including sound production by aquatic life (including all life forms that use aquatic habitats), reception of sound by aquatic life, effects of sound on aquatic life, scattering of sound from aquatic life, passive and active acoustic monitoring of aquatic life, and sound mapping.

 

This document defines technical concepts for unmanned stores and classifies them according to the degree of autonomy in their operations and/or services. It includes a definition, relevant actors, and a classification of unmanned stores. It also outlines the detailed operations and services by autonomy level, including those at unmanned stores.

 

This document specifies the complete specification operator for surface texture (scale-limited surfaces) by areal methods.

 

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.

 

 

This document describes a gas chromatographic method for determination of 5 chlorophenols (2-chlorophenol; 2,4-dichlorophenol; 2,4,6-trichlorophenol; 2,3,4,6-tetrachlorophenol; pentachlorophenol) in water samples. This method uses a liquid/solid extraction method using immersive solid phase extraction equipment. After sampling, retained organic compounds are released by thermal desorption (TD) and automatically transferred to a gas chromatography-mass spectrometry (GC-MS) system for analysis. NOTE 1 Other chlorophenols not specified in the scope can also be analysed if the performance specifications of this method can be met and the user validates the changes of the procedure accordingly. NOTE 2 The method detection limits (MDLs) of each chlorophenol measured by this method are shown in Annex B. This method is applicable to the determination of chlorophenols in surface water, ground water and drinking water. The applicability of the method to other types of water can be validated by the user separately for each individual case.

 

This document specifies requirements for blackplate product in the form of coils intended for direct use and mostly for the production of electrolytically zinc coated plate, or coils electrolytically coated with either tin (tinplate) or chromium/chromium oxide (ECCS or ECCS-RC). Blackplate can be a single or double reduced product and is specified in nominal thicknesses that are multiples of 0,005 mm from typical 0,10 mm up to 0,60 mm. This document applies to coils in nominal minimum widths of 600 mm. In addition to this document, the general technical delivery conditions of EN 10021 apply. NOTE Standard width coils for specific uses, e.g. tab stock, can be slit into narrow strip for supply in coil form.

 

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.

 

This document provides guidance on organizational purpose and governance of purpose-driven organizations - organizations that seek to align their decision-making and actions with the long-term wellbeing of all people and the planet. This document provides guidance to governing bodies on consciously directing, overseeing and accounting for how they govern their organizations so that it is purpose-driven. It is also intended to be relevant to stakeholders who provide services and support to organizations, or who invest in them, support them and help hold them to account for their purpose-driven commitments. It covers the worldviews, practices and behaviours of purpose-driven organizations and those that govern and influence them. This document is applicable to organizations of all types and sizes. This document does not provide guidance on organizational transformation processes.

 

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.

 

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.

 

This part of ISO 25178 specifies the complete specification operator for surface texture (scale limited surfaces) by areal methods.