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1 Scope This part of ISO 10993 specifies methodologies for the evaluation of the systemic toxicity potential of medical devices which release constituents into the body. In addition, it includes pyrogenicity testing. The test methods cited in this p

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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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This standard includes General Instruction #2. Scope This section of Part 2 of IEC Publication 60598 specifies requirements for luminaires for road and street lighting, for use with tungsten filament, tubular fluorescent, and other discharge lamps o

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1.1 Scope This section of Part 2 of IEC Publication 60598 specifies requirements for portable general purpose luminaires, other than handlamps, for use with tungsten filament, tubular fluorescent and other discharge lamps on supply voltages not exceedi

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1 Scope This part of ISO 10993 specifies allowable limits for residual ethylene oxide (EO) and ethylene chlorohydrin (ECH) in individual EO-sterilized medical devices, procedures for the measurement of EO and ECH, and methods for determining complian

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1 Scope This technical report contains guidelines regarding the safe and effective operation and maintenance on CARDIAC DEFIBRILLATORS, as defined in clause 3 below, to be performed by medical and nursing personnel. This report does not apply to autom

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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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1 Scope This technical report contains guidelines regarding the safe and effective operation and maintenance on HIGH FREQUENCY SURGICAL EQUIPMENT, as defined in clause 3, to be performed by medical and nursing personnel. The application guidelines i

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1 Scope This technical report contains guidelines regarding the maintenance on HIGH FREQUENCY SURGICAL EQUIPMENT, as defined in clause 3 below, to be performed by clinical engineering personnel. The application guidelines of this report deal with th

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CAN/CSA-Z259.2.1-98 (R2004) Fall Arresters, Vertical Lifelines and Rails 现行 发布日期 :  1970-01-01 实施日期 : 

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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