SFS Suomen Standardit

 

This document specifies the common conditions for plug and receptacle, rack to panel with interchangeable insulators and continuous temperature rating 150 °C.

 

This document specifies the general characteristics, the conditions for qualification, acceptance and quality assurance, as well as the test programs and groups for connectors intended for use in a temperature range from - 65 °C to 150 °C continuous.

 

This document specifies the minimum common safety and performance requirements of hand-held branchpipes used by fire and rescue service equipment. This document defines: - test methods; - classification and designation; - instructions for use and maintenance; marking. NOTE The additional specific requirements applicable to hand-held branchpipes are defined in EN 15182-2:— (combination branchpipes PN 16), EN 15182-3:— (Smooth bore and/or one fixed spray jet angle branchpipes PN 16) and EN 15182-4:— (High pressure branchpipes PN 40). This document is not applicable to: - branchpipes covered by the EN 671 series; - foam branchpipes covered by EN 16712-3; - CAFS branchpipes; - powder branchpipes; - branchpipes with a maximum working pressure above 40 bar.

 

In addition to common the requirements given in EN 15182 1, this document specifies the specific safety and performance requirements and the corresponding test methods, applicable to hand-held high pressure branchpipes (nozzles) with a nominal pressure of 40 bar (4,0 MPa) PN 40, with a maximum flow rate up to 250 l/min at a reference pressure of 6 bar (0,6 MPa). These branchpipes are used for example for quick attack lines, building fires, forest fires, etc.

 

In addition to the common requirements given in EN 15182 1, this document specifies the specific safety and performance requirements and the corresponding test methods, applicable to hand-held combination branchpipes (nozzles), with a nominal pressure of 16 bar (1,6 MPa) PN 16, with a maximum flow rate up to 1 000 l/min at a reference pressure of 6 bar (0,6 MPa).

 

In addition to the common requirements given in EN 15182-1, this document specifies the specific safety and performance requirements and the corresponding test methods, applicale to hand-held branchpipes with smooth bore and/or one fixed spray jet angle with a nominal pressure of 16 bar (1,6 MPa) PN 16, with a maximum flow rate up to 1 000 l/min at a reference pressure of 6 bar (0,6 MPa). NOTE 1 These branchpipes offer no or inadequate protection for firefighters when the spray jet angle is less than 30 ° and therefore are not adapted in high risk firefighting situations such as internal attack. NOTE 2 These branchpipes are not adapted when fighting fires in or near electrical installations when the spray jet angle is less than 30° without written authorization in the manual (safety distances included).

 

This document describes a test method for the determination of snagging resistance of a fabric using pins fitted in a rotating chamber.

 

ISO 10416:2008 provides procedures for the laboratory testing of both drilling-fluid materials and drilling-fluid physical, chemical and performance properties. It is applicable to both water-based and oil-based drilling fluids, as well as the base or “make-up” fluid. ISO 10416:2008 is not applicable as a detailed manual on drilling fluid control procedures. Recommendations regarding agitation and testing temperature are presented because the agitation history and temperature have a profound effect on drilling fluid properties.

 

This document defines subsets of the syntax specified in Recommendation ITU-T T.841.1 | ISO/IEC 26112-1 as profiles. It also defines lower bounds on the throughput in both the decoded and encoded domains via levels that a conforming decoder implementation shall support.

 

This document contains the reference software of the ITU-T T.841 | ISO/IEC 26112 series. It provides guidance for implementation of JPEG XE and as a reference for conformance testing.

 

This document specifies the information architecture required for interoperable communications between systems and services that need or provide EHR data. This document is not intended to specify the internal architecture or database design of such systems.

 

The subject of the record or record extract to be communicated is an individual person, and the scope of the communication is predominantly with respect to that person’s care.

 

Uses of healthcare records for other purposes such as administration, management, research and epidemiology, which require aggregations of individual people’s records, are not the focus of this document but such secondary uses could also find the document useful.

 

This document defines a set of interfaces to request and provide:

- an EHR_EXTRACT for a given subject of care as defined in ISO/DIS 13606-1 [1] ;

- one or more ARCHETYPE(s) as defined in ISO 13606-2 [2] ;

- an EHR_AUDIT_LOG_EXTRACT for a given subject of care as defined in ISO 13606-4 [3] .

 

This document defines the set of interactions to request each of these artefacts, and to provide the data to the requesting party or to decline the request. An interface to query an EHR or populations of EHRs, for example for clinical audit or research, are beyond its scope, although provision is made for certain selection criteria to be specified when requesting an EHR_EXTRACT which may also serve for population queries.

 

This document defines the Computational Viewpoint for each interface, without specifying or restricting particular engineering approaches to implementing these as messages or as service interfaces.

 

This document effectively defines the payload to be communicated at each interface. It does not specify the particular information that different transport protocols will additionally require, nor the security or authentication procedures that may be agreed between the communicating parties or required by different jurisdictions.

 

This document provides the principles, concepts, terms and definitions for health software and health IT systems, key properties of safety, effectiveness and security, across the full life cycle, from concept to decommissioning, as represented in Figure 1. It also identifies the transition points in the life cycle where transfers of responsibility occur, and the types of multi-lateral communication at these transition points. This document also establishes coherent concepts and terminology for other standards that address specific aspects of the safety, effectiveness, and security (including privacy) of health software and health IT systems.

 

This document is applicable to all parties involved in the health software and health IT systems life cycle including the following:

a) Organizations, health informatics professionals and clinical leaders designing, developing, integrating, implementing and operating health software and health IT systems – for example health software developers and medical device manufacturers, system integrators, system administrators (including cloud and other IT service providers);

b) Healthcare service delivery organizations, healthcare practitioners, subjects of care et al. who use health software and health IT systems for wellness, prevention, care, treatment or other health-related purposes;

c) Governments, healthcare system funders, monitoring agencies, professional organizations and customers seeking confidence in an organization’s ability to consistently provide safe, effective and secure health software, health IT systems and services;

d) Organizations and interested parties seeking to improve communication in managing safety, effectiveness and security through a common understanding of the concepts and terminology used in safety, effectiveness and security management;

e) Providers of training, assessment or advice in safety, effectiveness and security management for health software and health IT systems;

f) Developers of related safety, effectiveness and security standards.

 

This document specifies the technical delivery conditions for bends made by the cold bending process for bend with radii 5xOD or higher for use in pipeline transportation systems for the petroleum and natural gas industries as defined in ISO 13623. This document also specifies the requirements for the manufacture of two product specification levels (PSLs) of cold bends corresponding to product specification levels given for pipe in ISO 3183. This document is applicable to cold bends made from seamless and welded pipe of unalloyed or low-alloy steels. NOTE These are typically C-Mn steels or low-alloy steels that are appropriate for the corresponding level and grade of line pipe in accordance with ISO 3183. This document is not applicable to the selection of the cold bend product specification level. It is the responsibility of the purchaser to specify the PSL, based upon the intended use and design requirements. This document is not applicable to field cold bends and pipeline bends made by other manufacturing processes.

 

This document specifies the categorial structure within the field of traditional Chinese medicine clinical decision support system by defining a set of domain constraints of sanctioned characteristics, each composed of a relationship and an applicable information model. This document is not applicable to Western medicine and Japanese Kampo medicine. It is not applicable to the design and management of artificial intelligence diagnosis and treatment.

 

This document specifies requirements for the forensic process focusing on recognition, recording, collection, transport and storage of items of potential forensic value. It includes requirements for the assessment and examination of scenes but is also applicable to activities that occur within the facility. This document also includes quality requirements. This document is not applicable to procedures for the recovery of data from digital storage media which is covered by ISO/IEC 27037. However, the storage medium itself can yield additional items of forensic value (e.g. fingerprints or DNA). Annex D shows the applicability of this document to the forensic process.

 

This document specifies general requirements and recommendations for the operation of the forensic service provider. These apply throughout the forensic process, both at a scene and within a facility. This document also contains requirements and provides recommendations for the recovery and management of items. These requirements and recommendations are designed to ensure that: — items are preserved; — personnel are competent; — equipment and consumables are suitable; — health and safety risks are mitigated. This document is applicable to all areas of expertise of forensic science; however, it is not applicable to the recovery of digital data, which is covered by ISO/IEC 27037.[1] The storage medium itself can yield additional items (e.g. fingermarks or DNA) which would be covered by this document.

 

This document specifies the construction characteristics, performances and marking related to safety and the rational use of energy of portable, flat gas appliances directly supplied at the LPG vapour pressure, incorporating a gas cartridge complying with EN 417:2012, inserted horizontally in the chassis. NOTE 1 These appliances are referred to in the body of the text as “appliances”. This document covers appliances for outdoor or in well ventilated areas uses only. This document does not cover appliances supplied by an external gas source. For example, the following types of appliances are covered: a) cooking appliances (stoves, barbecues); b) heating appliances. This document specifies the requirements applicable to these appliances or their functional sections whether or not the latter are independent or incorporated into an assembly. Appliances covered by this document are not connected to a flue for the discharge of products of combustion and are not connected to the mains electricity supply. This document covers neither appliances supplied with LPG in the liquid phase nor appliance with fixed integral container which could be refilled by the user. This document does not cover appliances of direct pressure propane category. Requirements for rational use of energy have been considered for stove burners. NOTE 2 However, such requirements have not been considered for the other types of appliances because: - for barbecues, this type of cooking varies according to the type of food and region where the appliance is used; - for heating appliances, all the heat produced is discharged into the environment.

 

This document establishes a systematic description of the concepts in the field of biometrics pertaining to recognition of human beings. This document also reconciles variant terms in use in pre-existing International Standards on biometrics against the preferred terms, thereby clarifying the use of terms in this field. This document does not cover concepts (represented by terms) from information technology, pattern recognition, biology, mathematics, etc. Biometrics uses such fields of knowledge as a basis. In principle, mode-specific terms are outside of scope of this document.

 

This document specifies requirements, guidance and metrics for environmental impact evaluation of artificial intelligence systems and services and gives guidance on impact reduction throughout its Life cycle. This document establishes requirements and guidance on reporting and communicating about the environmental impact of AI. This document also provides techniques to evaluate potential indirect negative or positive consequences of AI systems and services, for stakeholders to anticipate or mitigate them. This document is applicable to the entire Life cycle of AI systems and services, from inception to end-of-life. This document is applicable to LCA practitioners conducting life-cycle analyses for AI systems or AI services, organizations developing and using AI systems or AI services (AI providers and deployers), and all actors in the value chain.

 

This document specifies the information architecture required for interoperable communications between systems and services that need or provide EHR data. This document is not intended to specify the internal architecture or database design of such systems.

 

The subject of the record or record extract to be communicated is an individual person, and the scope of the communication is predominantly with respect to that person's care.

 

Uses of healthcare records for other purposes such as administration, management, research and epidemiology, which require aggregations of individual people's records, are not the focus of this document but such secondary uses could also find the document useful.

 

This document defines a set of interfaces to request and provide:

— an EHR_EXTRACT for a given subject of care as defined in ISO 13606-1;

— one or more ARCHETYPE(s) as defined in ISO 13606-2;

— an EHR_AUDIT_LOG_EXTRACT for a given subject of care as defined in ISO 13606-4.

 

This document defines the set of interactions to request each of these artefacts, and to provide the data to the requesting party or to decline the request. An interface to query an EHR or populations of EHRs, for example for clinical audit or research, are beyond its scope, although provision is made for certain selection criteria to be specified when requesting an EHR_EXTRACT which might also serve for population queries.

 

This document defines the Computational Viewpoint for each interface, without specifying or restricting particular engineering approaches to implementing these as messages or as service interfaces.

 

This document effectively defines the payload to be communicated at each interface. It does not specify the particular information that different transport protocols will additionally require, nor the security or authentication procedures that might be agreed between the communicating parties or required by different jurisdictions.