Ämnesområden

This document defines the requirements for the design, manufacturing, quality control, assembly, testing, and documentation of ball, check, gate, plug, and axial on–off valves for application in subsea pipeline systems for the petroleum and natural gas industries. This document applies to ASME Class 150, 300, 600, 900, 1500, and 2500 valves intended for use in subsea pipelines. Use of these valves for any other purpose is outside the scope of this document. This document is a supplement to API 6DSS, 3rd edition (2022), the requirements of which are applicable with the additions specified in this document.

This document specifies requirements for the design, fabrication, inspection and testing of static vacuum-insulated cryogenic vessels designed for a maximum allowable pressure of more than 0,5 bar. This document applies to static vacuum-insulated cryogenic vessels for fluids and does not apply to vessels designed for toxic fluids. This document also gives guidance for static vacuum-insulated cryogenic vessels designed for a maximum allowable pressure of not more than 0,5 bar.

This International Standard specifies the minimum requirements for the design, manufacture and testing of centrifugal pumps for cryogenic service. This International Standard does not apply to reciprocating pumps. This International Standard also gives guidance on the design of installations (see Annex A). It does not specify requirements for operation or maintenance. NOTE For general requirements for materials used in cryogenic fluid service, see ISO 21029-1, ISO 20421-1 and/or ISO 21009-1.

ISO 12236:2006 specifies a method for the determination of the puncture resistance by measuring the force required to push a flat-ended plunger through geosynthetics. The test is normally carried out on dry specimens conditioned in the specified atmosphere. The test is applicable to most types of products, but not to materials with apertures greater than 10 mm.

Denna standard ersätter VIS 21 och skiljer sig därifrån genom att hål i plåt för ytterdörrar ändrats i konsekvens med ändrade höjder för dörrar, att hål i plåt för branddörrar, klass A, införts och att hål i plåt för innerdörrar av trä samt för kylrumsdörrar utgått.

Angivna tröskelhöjder på sidan 3 är godkända av Sjöfartsverket, Sjöfartsdirektoratet (Norge), Det norske Veritas och Lloyds Register of Shipping.

I händelse av tvist om tolkningen av denna standard skall den svenska versionen gälla före den engelska översättningen.

Denna standard omfattar metoder för hållfasthetsprovning av dörrar.

Standarden omfattar två metoder.

Metod 1, vakuummetod, för belastningar t o m 0,06 N/mm2

Metod 2, tryckmetod, for belastningar t o m 0,25 N/mm2.

Provningsmetoderna gäller som rekommendation i avvaktan på närmare erfarenheter från tillämpningen.

Överenskommelse om tillämpning får träffas mellan tillverkare, köpare och berörd myndighet i varje enskilt fall.

Standarden överensstämmer med motsvarande standarder i de övriga nordiska länderna

1 N/mm2 = 1 MPa

I händelse av tvist om tolkningen av denna standard skall den svenska versionen gälla före den engelska översättningen.

This document specifies an extensible markup language (XML) format to facilitate the transfer of dental case data and CAD/CAM data between software systems.

This document specifies polymers commonly used in manufacturing dental instruments. It is applicaple to polymers materials used to manufacture either an entire instrument or a part of the instrument. It is applicable to single-use and reusable dental instruments, connected to a power-driven system or not. This document is not applicable to devices and instruments used long-term in the mouth of the patient (e.g. crown, bridges, implants) or to devices and instruments not made of polymers. It contains a current selection of polymers suitable for use in the manufacture of dental instruments.

This standard provides guidelines for the selection and implementation of pipeline geohazards monitoring methods and strategies. It provides processes and principles applicable to various practical monitoring measures. Moreover, it describes the methods and procedures to be implemented and provides guidance for determining the: —type, significance grade and frequency of monitoring; —recommended monitoring objects and appropriate monitoring systems and methods; —components of the monitoring system; —threshold alarms, early warning level, criteria and response measures; —requirements of the early warning information system. This standard applies to onshore gathering and transmission pipelines used in the petroleum and natural gas industries.

This standard specifies the base set of Participant Key Purposes (PKPs) for the Service-oriented Device Connectivity (SDC) series of standards. PKPs are role-based sets of requirements for products in order to support safe, effective, and secure interoperability in medical IT networks at point-of-care environments such as the intensive care unit (ICU), operating room (OR) or other acute care settings. This standard specifies both product development process and technical requirements.

ISO/IEEE 11073-10471:2010 establishes a normative definition of the communication between independent living activity hubs and managers (e.g., cell phones, personal computers, personal health appliances and set top boxes) in a manner that enables plug-and-play (PnP) interoperability. It leverages appropriate portions of existing standards including ISO/IEEE 11073 terminology and information models. It specifies the use of specific term codes, formats, and behaviors in telehealth environments restricting ambiguity in base frameworks in favour of interoperability. ISO/IEEE 11073-10471:2010 defines a common core of communication functionality for independent living activity hubs. In this context, independent living activity hubs are defined as devices that communicate with simple situation monitors (binary sensors), normalize information received from the simple environmental monitors, and provide this normalized information to one or more managers. This information can be examined (for example) to determine when a person's activities/behaviour have deviated significantly from what is normal for them such that relevant parties can be notified. Independent living activity hubs will normalize information from the following simple situation monitors (binary sensors) for the initial release of the proposed standard: fall sensor, motion sensor, door sensor, bed/chair occupancy sensor, light switch sensor, smoke sensor, (ambient) temperature threshold sensor, personal emergency response system (PERS), and enuresis sensor (bed-wetting). ISO/IEEE 11073-10471:2010 addresses a need for an openly defined, independent standard for controlling information exchange to and from personal health devices and managers

Within the context of the ISO/IEEE 11073 family of standards for device communication, ISO/IEEE 11073-10472:2012 establishes a normative definition of communication between personal telehealth medication monitor devices and compute engines (e.g. cell phones, personal computers, personal health appliances, set top boxes) in a manner that enables plug-and-play interoperability. It leverages appropriate portions of existing standards including ISO/IEEE 11073 terminology, information models, application profile standards, and transport standards. It specifies the use of specific term codes, formats, and behaviors in telehealth environments restricting optionality in base frameworks in favor of interoperability. ISO/IEEE 11073-10472:2012 defines a common core of communication functionality for personal telehealth medication monitor devices.

This standard specifies a set of Participant Key Purposes (PKPs) pertaining to metric data exchange for the Service-oriented Device Connectivity (SDC) series of standards. PKPs are role-based sets of requirements for products in order to support safe, effective, and secure interoperability in medical IT networks at point-of-care environments such as the intensive care unit (ICU), operating room (OR) or other acute care settings. This standard specifies both product development process and technical requirements.

This standard establishes a normative definition of communication between personal health continuous glucose monitor (CGM) devices (agents) and managers (e.g., cell phones, personal computers, personal health appliances, set top boxes) in a manner that enables plug-and-play interoperability. It leverages work done in other ISO/IEEE 11073 standards including existing terminology, information profiles, application profile standards, and transport standards. It specifies the use of specific term codes, formats, and behaviors in telehealth environments, restricting optionality in base frameworks in favor of interoperability. This standard defines a common core of communication functionality of CGM devices. In this context, CGM refers to the measurement of the level of glucose in the body on a regular (typically 5 minute) basis through a sensor continuously attached to the person.

and cereal products. This document applies to: wheat, rice (paddy, husked and milled), barley, millet (Panicum miliaceum), rye, oats, triticale, sorghum in the form of grains, milled grains, semolina or flour. The method is not applicable to maize and pulses. NOTE For moisture content determination in maize, see ISO 6540[5]; and for pulses, see ISO 24557[7].

This document specifies a test method and the minimum requirements for the microbicidal activity of a specified disinfection process for the treatment of contaminated textile. This procedure is carried out by using a washing machine as specified in 5.3.2.18 and refers to the disinfection step without prewash. This procedure is not limited to certain types of textile. The suppliers' instructions are expected to be sufficient if they content the process parameters identified in the test (e.g. dosing disinfectant in whatever washing phase e.g. main wash, rinsing, disinfecting at 40 °C). This document applies to areas and situations where disinfection is medically indicated. Such indications occur in patient care, for example: - in hospitals, in community medical facilities, and in dental institutions; - in clinics of schools, of kindergartens, and of nursing homes; and could occur in the workplace and in the home. It could also include services such as laundries and kitchens supplying products directly for the patients. The method described is intended to determine the activity of a product or product combination under the conditions in which they are used. This is a phase 2, step 2 laboratory test that simulates the conditions of application of the product. EN 14885 specifies in detail the relationship of the various tests to one another and to “use recommendations”.

This document covers hinged and pivoted steel (any kind) and aluminium based framed, glazed doorsets or openable windows. Throughout this document, the term "doorset" will be used to cover both doorsets and door assemblies. It prescribes the methodology for extending the application of test results obtained from fire resistance test(s) conducted in accordance with EN 1634-1. Subject to the completion of the appropriate test or tests selected from those identified in Clause 4, the extended application can cover all or some of the following examples: - integrity (E), integrity & radiation (EW) or integrity & insulation (EI1 or EI2) classification, - glazed elements including vision panels and framed glazed doorsets, - air transfer grilles (louvres and/or vents), - side, transom or over panels, - items of building hardware, - decorative and protective finishes, - intumescent seals and non-intumescent (smoke, draught or acoustic) seals, - alternative supporting construction(s). This document does not cover horizontal doorsets. The effect on the Classification ‘C’ for the doorsets following an extended application process is not addressed in this document.

 This document specifies a method for the photometric determination of dissolved chromium(VI) using manual, e.g., hand photometry, or automated static, e.g., discrete analyser system, or automated dynamic techniques, e.g., flow injection analysis (FIA), continuous flow analysis (CFA), or ion chromatography with post-column derivatization (IC-PCR). The choice of the analytical technique to be used and needs-based sample preparation (e.g., matrix elimination) enables the determination of chromium(VI) in concentrations ≥0,02 µg/l in raw water, drinking water, surface water, aqueous eluates, cooling water and treated wastewater, provided that the Matrix does not contain any reducing substances. Typical areas of application for the static techniques as well as FIA and CFA are samples with chromium(VI) concentrations ≥2 µg/l. When using cuvettes with large optical path lengths, e.g. >100 mm, the range of application can be extended to concentrations <2 µg/l chromium(VI) (Annex A; Annex B; Annex C, Clauses C.1 and C.2). When using coupled techniques (e.g. IC PCR), chromium(VI) concentrations ≥0,02 µg/l can be determined (Annex C, Clause C.3). In some waters with reducing ingredients, chromium(VI) losses can occur just a few hours after sampling. Therefore, the method was not validated for leachate from landfills and raw sewage.

This document provides definitions, guidelines and supportive information for characterization methods and key performance parameters of absorption liquids used in post-combustion CO2 capture

This document considers atmospheric precipitation and defines the procedures and equipment to perform laboratory and field tests, in steady-state conditions, for the calibration, check and metrological confirmation of non-catching precipitation measurement instruments. It provides a classification of non-catching measurement instruments based on their laboratory performance. The classification does not relate to the physical principle used for the measurement, nor does it refer to the technical characteristics of the instrument assembly but is solely based on the instrument calibration. Attribution of a given class to an instrument is not intended as a high/low ranking of its quality but rather as a quantitative standardized method to declare the achievable measurement accuracy to provide guidance on the suitability for a particular purpose, while meeting the user’s requirements.