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This clause of Part 1 is replaced by the following. This International Standard deals with the safety of electric range hoods and other cooking fume extractors intended for installing above, beside, behind or under household...

1) The International Electrotechnical Commission (IEC) is a worldwide organization for standardization comprising all national electrotechnical committees (IEC National Committees). The object of IEC is to promote...

This Standard applies to movable, stationary, fixed or built-in UPS for use in low-voltage distribution systems and that are intended to be installed in an area accessible by an ordinary person or in a restricted access area...

This clause of Part 1 is replaced by the following. This International Standard deals with the safety of electric range hoods and other cooking fume extractors intended for installing above, beside, behind or under household...

This clause of Part 1 is replaced by the following. This International Standard deals with the safety of electric range hoods and other cooking fume extractors intended for installing above, beside, behind or under household...

CSA intends to publish a national standard that will provide the foundation for a comprehensive Canadian Paramedic Information System (CPIS). This standard will be based on frameworks, common taxonomies and designs and...

This part of lEC 60320 sets the general requirements for appliance couplers for two poles and two poles with earth contact and for the connection of electrical devices for household and similar onto the mains supply. This...

CAN/ULC-S531 and ANSI/UL 217 are being merged into a single binational standard that can be used for Canada and the United States, Although the standards have mostly identical requirements, there are some that are unique to...

This clause of Part 1 is replaced by the following. This International Standard deals with the safety of electric tumble dryers intended for household and similar purposes, their rated voltage being not more than 250 V for...

This document specifies requirements for the information to be provided by the medical device manufacturer for the processing of critical or semi-critical medical devices (i.e. a medical device that enters normally sterile...