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1 Scope This document outlines a generic process for developing materials for education and training of operators of medical electrical equipment. It may be used by standards organizations, manufacturers, regulatory agencies, hospital managers, clinic

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This standard includes Update #2. 1.1 Scope This section of Part 2 of IEC Publication 598 specifies requirements for fixed general purpose luminaires for use with tungsten filament, tubular fluorescent and other discharge lamps on supply voltages n

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This PDF includes General Instruction #2. 1. Domaine d'application Cette section de la deuxième partie de la Publication 598 de la CEI détaille les prescriptions applicables aux luminaires pour l'éc lairage des scènes de théatre, des studios de télé

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1. Scope This section of Part 2 of IEC 598 specifies requirements for fixed luminaires intended for use in water, or in contact with water, in, for example, the basins of swimming pools, fountains, paddling pools, and garden pools, and for use with tun

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This PDF includes General Instruction No. 2 1. Scope This section of Part 2 of IEC Publication 598 specifies safety requirements for air-handling luminaires for use with a ventilation duct or ventilated space (plenum), for use with tubular fluoresce

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8.1 Scope This section of part 2 of IEC 598 specifies requirements for handlamps and similar portable luminaires which are held in the hand when used, for use with tungsten filament and tubular fluorescent lamps on supply voltages not exceeding 250 V. It

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1 Scope This part of ISO 10993 describes test methods: (a) to evaluate the potential of devices and their constituent materials to produce irritation; and (b) to evaluate the potential of devices and their constituent materials to produce sensitizat

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1 Scope This part of ISO 10993 specifies requirements and gives guidance on procedures to be followed in the preparation of samples of medical devices for testing in biological systems in accordance with one or more other parts of ISO 10993. These inc

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1. Scope 1.1 This Guide covers the consideration of environmental impacts in product standards. It is intended for standard w riters; its purpose is (a) to raise awareness that provisions in product standards can affect the environment in both nega

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This PDF includes Updates #2, #3 and #4. 1. Scope 1.1 This Standard provides design and performance requirements for manufactured fall-arresting devices, vertical lifelines, and rigid sections, including mounting components. 1.2 The equipment sp

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This PDF includes Updates #2 and #3 1. Scope 1.1 This Standard specifies the requirements for all self-retracting devices (SRDs) used as connecting components in personal fall-arrest systems. SRDs are further classified in this Standard according t

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CAN/CSA-Z364.1.3-98 (R2004) Reuse of Haemodialysers 现行 发布日期 :  实施日期 : 

Update #2 was published as notification that this is now a national standard of Canada. 1. Scope 1.1 This Standard details the essential elements of good pract ice for reprocessing haemodialysers. It is intended to provide the administrator with a

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1 Scope This technical report contains guidelines regarding maintenance to be performed on CARDIAC DEFIBRILLATORS, as defined in clause 3 below, by clinical engineering personnel. This report does not apply to automatic implantable DEFIBRILLATORS and

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