Rechercher

1.1 General 1.1.1 This Standard provides guidelines for the commissioning of buildings and all energy and domestic water related building systems. It applies to new construction only for Part 3 buildings, as specified in the National Building Code of Canada (NBC). It does not apply to equipment and systems installed by the owner or others after building completion. 1.1.2 This Standard is intended…

1.1 This Standard, following the principles set out in CAN/CSA-Z1000, specifies requirements for a) establishing and maintaining an extreme conditions management system in accordance with occupational health and safety management system (OHSMS) principles; b) the roles and responsibilities of the management representative, the monitoring team, and the worker; c) management of external service…

This part of IEC 61000 specifies EMC immunity requirements which apply to electrical and electronic equipment intended for use in power stations and substations, as described below. Immunity requirements for electromagnetic phenomena with spectral contributions in the frequency range 0 Hz to 400 GHz are covered. No tests need to be performed at frequencies or for phenomena where no requirements…

This clause of Part 1 is applicable, except as follows. 1.1.1 Equipment included in scope Replacement: • This part of IEC 61010 specifies safety requirements and related verification tests for any product performing the function of control equipment and/or their associated peripherals. In addition, these products have as their intended use the command and control of machines, automated…

1.1 Inclusions This Standard is intended to be used for industrial refrigeration systems using refrigerants such as R22, R404A, R448a, R410a, and ammonia (R717) and with the following characteristics: a) facility types including storage warehouses, distribution facilities, and refrigerated processes; b) facility storage volume equal to or greater than 283 m3 (10,000 ft3); and c) process…

1.1 This Standard is intended to address the safe, effective, and reliable reprocessing of reusable medical devices at each phase of the reprocessing workflow, including a) establishing a QMS for the MDRD, including i) key performance indicators; ii) policies and procedures; iii) documentation; iv) roles and responsibilities; v) management review; vi) planning, resources and operations…

ISO 10524-2:2018 specifies design, construction, type testing, and marking requirements for manifold pressure regulators (as defined in 3.7) and line pressure regulators (as defined in 3.5) intended for use in medical gas pipeline systems. Examples of gases include oxygen, medical air and oxygen/nitrous oxide mixtures. ISO 10524-2:2018 applies to manifold pressure regulators and line pressure…

ISO 10524-1:2018 specifies the design, construction, type testing, and marking requirements for pressure regulators (as defined in 3.18) intended for the administration of medical gases and their mixtures in the treatment, management, diagnostic evaluation and care of patients or for gases used for driving surgical tools. Examples of gases include oxygen, medical air and oxygen/nitrous oxide…

ISO 12944-6:2018 specifies laboratory test methods and test conditions for the assessment of paint systems for the corrosion protection of carbon steel structures. The test results are intended to be considered as an aid in the selection of suitable paint systems and not as exact information for determining durability. ISO 12944-6:2018 covers protective paint systems designed for application to…

ISO 12944-9:2018 specifies the performance requirements for protective paint systems for offshore and related structures (i.e. those exposed to the marine atmosphere, as well as those immersed in sea or brackish water). Such structures are exposed to environments of corrosivity category CX (offshore) and immersion category Im4 as defined in ISO 12944‑2. ISO 12944-9:2018 describes paint systems…