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IEC 61010-2-202:2016 specifies the safety requirements for electric ACTUATORs and SOLENOIDs, as applied to valves, intended to be installed in an industrial process or discrete control environment. This publication is to be read in conjunction with IEC 61010-1:2010.

ISO 18642:2016 specifies the general requirements regarding testing methods, sampling and preparation of test sample, marking and labelling, package, transport, and storage of fertilizer grade urea. It is applicable to urea in solid form, e.g. granular, prilled, or pastilled, which is made by the reaction of ammonia with carbon dioxide. Urea can be classified by its intended use, industrial and/…

IEC TR 63039:2016(E) provides guidance on probabilistic risk analysis (hereafter referred to as risk analysis) for the systems composed of electrotechnical items and is applicable (but not limited) to all electrotechnical industries where risk analyses are performed. This document deals with the following topics from the perspective of risk analysis: - defining the essential terms and concepts…

This is the first edition of CAN/CSA-C22.2 No. 62109-1, Safety of power converters for use in photovoltaic power systems — Part 1: General requirements, which is an adoption, with Canadian deviations, of the identically titled IEC (International Electrotechnical Commission) Standard 62109-1 (first edition, 2010-04). It is one in a series of Standards issued by CSA Group under Part II of the…

This is the first edition of CAN/CSA-C22.2 No. 62109-2, Safety of power converters for use in photovoltaic power systems — Part 2: Particular requirements for inverters, which is an adoption, with Canadian deviations, of the identically titled IEC (International Electrotechnical Commission) Standard 62109-2 (first edition, 2011-06). It is one in a series of Standards issued by CSA Group under…

La présente partie de l’ISO 11607 spécifie les exigences et les méthodes d'essai pour les matériaux, les systèmes de barrière stérile préformés, les systèmes de barrière stérile et les systèmes d'emballage destinés à maintenir l'état de stérilité des dispositifs médicaux stérilisés au stade terminal jusqu'au point d'utilisation. La présente partie de l’ISO 11607 s…

1.1 This Standard specifies criteria to develop emission reduction practices and programs. 1.2 This Standard addresses fugitive and vented emissions from point sources in the following sectors (see Figure 1) of the upstream oil and gas industry from wells, pipelines, and facilities associated with a) crude oil production and shale oil; b) oil sands – in situ bitumen production, including…

1 Scope This part of ISO 11607 specifies the requirements for development and validation of processes for packaging medical devices that are terminally sterilized. These processes include forming, sealing, and assembly of preformed sterile barrier systems, sterile barrier systems and packaging systems. This part of ISO 11607 is applicable to industry, to health care facilities, and wherever…

1 Domaine d'application La présente partie de l'ISO 11607 spécifie les exigences pour la mise au point et la validation des procédés d’emballage de dispositifs médicaux qui sont stérilisés au stade terminal. Ces procédés comprennent le formage, le scellage et l’assemblage de systèmes de barrière stérile préformés, de systèmes de barrière stérile et de systèmes d’emballage. La…

L'ISO 16170 :2016 spécifie les méthodes d'essai in situ des filtres à très haute efficacité des particules contenues dans l'air utilisés afin de limiter les rejets dans l'environnement (par exemple, installations nucléaires ou installations rejetant des aérosols toxiques ou biologiques). Ceci s'applique lorsque des installations comprenant ces filtres sont utilisées, dans…