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1.1 This procedure defines the long-term thermal resistance (LTTR) of a foam product as the value measured after 5-year storage in a laboratory environment and provides means for its prediction based on an accelerated...

This method of test for flammability characteristics is applicable to certain low density insulating materials that do not melt or drip during exposure to fire (see Appendix A). It is used in establishing the Flame Spread...

1.1 This Standard provides minimum requirements for primary containment leak detection that uses quantitative assessment of physical characteristics to detect leaks in the primary containment. 1.2 These requirements do not...

1.201 Scope This Collateral Standard applies to the SAFETY of MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS incorporating PROGRAMMABLE ELECTRONIC SUBSYSTEMS (PESS), hereinafter referred to as PROGRAMMABLE...

The goal of the guideline is to provide methods for modellers that result in an accurate as possible energy model. This goal can best be achieved if the guideline is a ‘living document,’ changing and growing as increasing...

1.1 This Standard is intended to be read together with Annex A, Ref. No. 1. The requirements of Annex A, Ref. No. 1 apply unless modified by this Standard

This Standard specifies the requirements and test methods for low pressure applied two component medium density spray polyurethane thermal insulation foam used as a thermal insulation for both building and non-building...

These requirements cover the construction and operation of water-based automatic extinguisher units intended for total flooding applications when installed, inspected, tested, and maintained in accordance with the...

These requirements cover components intended for use in the manufacturer of personal flotation devices. Compliance with these requirements does not indicate that the product is intended for use as a component of an end...

This security evaluation standard applies to the testing of network connected components of healthcare systems. It applies to, but is not limited to, the following key components: a) Medical devices; b) Accessories to medical...

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...

1.1 This Standard is intended to be read together with Annex A, Ref. No. 1. The requirements of Annex A, Ref. No. 1 apply unless modified by this Standard.