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This National Standard of Canada is equivalent to International Standard ISO 10993-7:1995. 1 Scope This part of ISO 10993 specifies allowable limits for residual ethylene oxide (EO) and ethylene chlorohydrin (ECH) in individual EO-sterilized medical devices, procedures for the measurement of EO and ECH, and methods for determining compliance so that devices may be released. Additional…

This National Standard of Canada is equivalent to International Standard ISO 10993-10:1995. 1 Scope This part of ISO 10993 describes test methods: a) to evaluate the potential of devices and their constituent materials to produce irritation; and b) to evaluate the potential of devices and their constituent materials to produce sensitization. These test methods are…

This National Standard of Canada is based on International Standard CEI/IEC 598-2-18:1993 (second edition, 1993-04). 1. Scope This section of Part 2 of IEC 598 specifies requirements for fixed luminaires intended for use in water, or in contact with water, in, for example, the basins of swimming pools, fountains, paddling pools, and garden pools, and for use with tungsten filament lamps…

This National Standard of Canada is equivalent to International Standard ISo 10993-1:1992. 1 Scope This part of ISO 10993 gives guidance on a) the fundamental principles governing the biological evaluation of medical devices; b) the definition of categories of devices based on the nature and duration of contact with the body; c) the selection of appropriate tests. ISO 10993 does not cover…

This National Standard of Canada is equivalent to International Standard ISO 10993-4:1992. 1 Scope This part of ISO 10993 gives guidance to agencies, manufacturers, research laboratories and others for evaluating the interactions of medical devices with blood. It describes: a) a classification of medical and dental devices that are intended for use in contact with blood, based…

This National Standard of Canada is equivalent to International Standard ISO 10993-5:1992. 1 Scope This part of ISO 10993 describes test methods to assess the in vitro cytotoxicity of medical devices. NOTE 1 The term medical devices corresponds to the definition given in ISo 10993-1 and covers medical materials as well as dental material and devices. The definition is in accordance…

This National Standard of Canada is equivalent to International Standard ISO/IEC 7816-4:1995. 1 Scope This part of ISO/IEC 7816 specifies - the content of the messages, commands and reponses, transmitted by the interface device to the card and conversely, - the structure and content of the historical bytes sent by the card during the answer to…

The international community has decided to make this standard available only in the English language version. It has been adopted as a National Standard of Canada on this basis. This National Standard of Canada is equivalent to International Standard ISO/IEC 13575:1995. 1 Scope This International Standard specifies a 50-pole connector, including the necessary mateability…

1.1 SCOPE 1.1.1 This standard applies to newly produced Type 1 clothes dryers (see Part IV, Definitions), hereinafter referred to as dryers, constructed entirely of new, unused parts and materials: a. For use with natural gas, b. For use with manufactured gas, c. For use with mixed gas, d. For use with liquefied petroleum gases…

This National Standard of Canada is equivalent to International Standard ISo 4903:1989. 1 Scope This International Standard specifies the 15-pole connector and the assignment of contact numbers at the interface between data terminal equipment (DTE) and data circuit-terminating equipment (DCE) where CCITT 1) Recommendations X.24, X.26, and X.27 are applicable. International Standard ISO/IEC…