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1. Scope This standard addresses the construction and use of test suites for verifying conformance of SGML systems. Its provisions assist those who build test suites, those who build SGML systems to be evaluated by such...

1.1 This method of test is applicable to firestop systems with or without penetrating items such as cables, cable trays, conduits, ducts and pipes. These firestop systems are intended for use in openings in fire resistive...

This International Standard applies to the reduction of adverse ENVIRONMENTAL IMPACTS of MEDICAL ELECTRICAL EQUIPMENT, hereafter referred to as ME EQUIPMENT. MEDICAL ELECTRICAL SYSTEMS are excluded from the scope of this...

These requirements apply to single and multiple jacketed lined fire hose of the following nominal inside diameter trade sizes: 38, 45, 50, 65, 77, 89, 100, 125 and 150 mm (1-1/2, 1-3/4, 2, 2-1/2, 3, 3-1/2, 4, 5, and 6 inch)...

ASME A17.8/CSA B44.8 applies to elevators permanently installed in a wind turbine tower to provide vertical transportation of authorized personnel and their tools and equipment only. Such elevators are typically subjected to...

This Standard addresses the construction and use of test suites for verifying conformance of SGML systems. Its provisions assist those who build test suites, those who build SGML systems to be evaluated by such suites, and...

.1 This part of ISO/IEC 18000 defines the generic architecture concepts in which item identification may commonly be required within the logistics and supply chain and defines the parameters that need to be determined in any...

1.1 This part of ISO/IEC 18000 defines the generic architecture concepts in which item identification may commonly be required within the logistics and supply chain and defines the parameters that need to be determined in any...

This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, design, VERIFY and VALIDATE USABILITY, as it relates to BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT, hereafter...

These requirements cover air filter units of both washable and throw-away types for removal of dust and other airborne particles from air circulated mechanically in equipment and systems.

This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, design, VERIFY and VALIDATE USABILITY, as it relates to BASIC SAFETY and ESSENTIAL PERFORMANCE of MEDICAL ELECTRICAL EQUIPMENT, hereafter...

These requirements cover air filter units of both washable and throw-away types for removal of dust and other airborne particles from air circulated mechanically in equipment and systems.