1 Scope This part of ISO 11140 specifies performance requirements for indicators that show exposure to sterilization processes by means of physical and/or chemical change of substances. NOTE 1 These indicators are used to monitor the presence or at

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This PDF includes GI #2. 1. Scope This Specification is intended to apply to power-operated radio transmitting equipment designed to be used on standard supply circuits in accordance with the rules of Part I of this Code. This will include all typ

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1. Scope and Objectives 1.1 Scope This Standard applies to suspension and dead-end composite insulators used on ac overhead transmission lines with a nominal voltage 69 kV or greater and a frequency not greater than 100 Hz. 1.2 Objectives The

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1. Scope This International Standard applies to residual current operated circuit-breakers functionally independent of, or functionally dependent on, line voltage, for household and similar uses, not incorporating overcurrent protection (hereafter refe

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1.1 Scope This Standard applies to the safety of tungsten filament lamps intended for use in lighting equipment, designed to be installed on branch circuits not exceeding 750 V and used in accordance with the rules of the Canadian Electrical Code (CEC

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1 Scope This International Standard specifies requirements for the use of moist heat in sterilization process development, validation of the sterilization process and control of routine sterilization. It covers all moist heat processes, including sa

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1 Scope 1.1 This International Standard establishes requirements and guidance for validation and routine control of ethylene oxide sterilization processes for medical devices. Particular attention is drawn to the need for specific testing for safe

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1 Scope This International Standard specifies requirements for validation, process control and routine monitoring in the r adiation sterilization of health care products. It applies to continuous and batch type gamma irradiators using the radionuclide

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1 Scope 1.1 This International Standard specifies tests to be performed and requirements for test apparatus to be used in determining the physical, biological and mechanical properties of heart valve substitutes of all types, and of the materials and

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1. Scope 1.1 The purpose of this Standard is to facilitate identification, by class, of drugs in syringes filled by the user that are used in anaesthesia and critical care. 1.2 This Standard specifies design requirements for the size, shape, patte

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1. Scope This section of Part 2 of IEC Publication 598 specifies requirements for portable child-appealing luminaires for use with tungsten filament lamps on supply voltages not exceeding 24 V (SELV). It is to be read in conjunction with those sections

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1. Scope This section of IEC 598-2 specifies requirements for recessed luminares for use with tungsten filament, tubular fluorescent and other discharge lamps on supply voltage not exceeding 1000 V. This section does not cover air-handling luminaires.

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