Scope
1.1
This Standard specifies technical requirements for the design, construction, testing, inspection, and performance of relocatable above-ground collapsible fabric storage tanks (bladders) intended for the storage of petroleum products and allied petroleum products with a relative density not greater than 1.
1.2
This Standard applies to bladders that are shop-fabricated from reinforced…
Asphalt shingle application on roof slopes 1:6 and steeper
Scope
1.1
This Standard provides minimum requirements for the application of asphalt shingles on roofs with a slope of 1:6 and steeper.
Portions of this Standard may not apply to laminated and/or dimensional shingles. The manufacturers of these shingles should be consulted for specific installation instructions.
Note: Annex A is included to provide recommendations for acceptable…
Scope
1.1
This Standard specifies the energy performance test method for room air conditioners and specifies minimum efficiency levels.
1.2
This Standard covers room air conditioners powered by a single-phase electric current and rated at 10.55 kW (36 000 Btu/h) cooling capacity and below at standard rating conditions.
1.3
This Standard does not apply to the rating and testing of individual…
Household and similar electrical appliances - Safety - Part 2-44: Particular requirements for ironer...
Scope
This clause of Part 1 is replaced by the following.
This International Standard deals with the safety of electric ironers for household and similar purposes, their rated voltage being not more than 250 V for single-phase appliances and 480 V for other appliances.
Appliances not intended for normal household use but which nevertheless may be a source of danger to the public, such as…
Scope
1.1
This Standard specifies the requirements for all self-retracting devices (SRDs) used as connecting components in fall protection systems. SRDs are further classified in this Standard according to method of use.
1.2
The equipment specified in this Standard is intended for users at risk of falls from height while at work.
1.3
This Standard outlines requirements for labeling products…
Plumbing fixtures with pumped waste and macerating toilet systems
Scope
1.1
This Standard establishes physical, performance, and testing requirements applicable to plumbing fixtures with pumped waste, macerating toilet systems, and related components. Such systems are intended to collect waste from a single fixture such as a water closet, lavatory, shower, or bathtub and pump these wastes to some point in the sanitary drainage system.
1.2
The purpose of…
Scope
1.1
This Standard specifies the requirements for cord sets and power-supply cords employing molded-on or assembled-on fittings, rated 600 V maximum, and intended for use in non-hazardous locations in accordance with the Canadian Electrical Code, Part I, CSA C22.1-12 and General Requirements-Canadian Electrical Code, Part II, CSA C22.2 No. 0-10.
1.2
This Standard also specifies the…
Automatic electrical controls for household and similar use - Part 2-5: Particular requirements for ...
1 Scope and normative references
This clause of part 1 is applicable except as follows:
1.1 Replacement:
This part of IEC 60730 applies to automatic electrical burner control systems for the automatic control of burners for oil, gas, coal or other combustibles for household and similar use including heating, air conditioning and similar use.
This part 2-5 is applicable to a complete…
Medical device software - Software life cycle processes (Adopted CEI/IEC 62304:2006, first edition, ...
Scope
1.1 * Purpose
This standard defines the life cycle requirements for MEDICAL DEVICE SOFTWARE. The set of PROCESSES, ACTIVITIES, and TASKS described in this standard establishes a common framework for MEDICAL DEVICE SOFTWARE life cycle PROCESSES.
1.2 * Field of application
This standard applies to the development and maintenance of MEDICAL DEVICE SOFTWARE.
This standard applies to the…
Medical devices - Application of usability engineering to medical devices (Adopted IEC 62366:2007, f...
1 * Scope
This International Standard specifies a PROCESS for a MANUFACTURER to analyse, specify, design, VERIFY and VALIDATE USABILITY, as it relates to SAFETY of a MEDICAL DEVICE. This USABILITY ENGINEERING PROCESS assesses and mitigates RISKS caused by USABILITY problems associated with CORRECT USE and USE ERRORS, i.e. NORMAL USE. It can be used to identify but does not assess or mitigate…