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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...

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

1.1 These requirements cover exhaust hoods for commercial and institutional kitchens and are intended for placement over restaurant type cooking equipment, such as ranges, broilers, deep fat fryers, grills, etc., during...

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 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...

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...

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...

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.

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...

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