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Specifies the requirements for infusion pumps, infusion controllers, syringe pumps and pumps for ambulatory use. These devices are intended for use by medical staff and home patients as prescribed and medically indicated. It is the responsibility of the manufacturer to ensure that the requirements of this standard are reliably implemented.

Specifies terminology and test methods for declaring the characteristics of positron emission tomographs. Positron emission tomographs detect the annihilation radiation of positron emitting radionuclides by coincidence detection. It is intended that the test methods be carried out by the manufacturers, thereby enabling them to declare the characteristics of positron emission tomographs. So, the…

States and defines the principal performance characteristics of vacuum cleaners which are of interest to the user and describes the standard methods for measuring these characteristics.

1. Scope 1.1 This Standard provides energy and lighting performance requirements for highmast luminaires using high-pressure sodium (HPS) lamps. 1.2 This Standard applies to highmast luminaires used along streets, roadways, highways, and expressways, at intersections, and at interchanges in standard layout arrangements. 1.3 The minimum requirements established by this Standard are based on…

1. Scope 1.1 This Standard describes in POSIX terms the minimal parameters needed to localize Canadian software. Any software application distributed in Canada should be designed to conform to the presentation rules in use in Canada whether or not the software uses interfaces that comply with a POSIx environment. Those rules are described in this Standard. 1.2 This Standard does not impose…

This National Standard of Canada is equivalent to International Standard ISo 5841/2-1986. 1 Scope and field of application This part of ISO 5841 specifies requirements for reports on the clinical performance in humans of population samples of pulse generators. It includes general requirements for all reports and supplementary requirements for reports on recent experience and…

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 ISP 10607-1:1995. 1 Scope 1.1 General This part of ISO/IEC ISP 10607 specifies how the Association Control Service Element…

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 9798-4:1995. 1 Scope This part of ISO/IEC 9798 specifies entity authentication mechanisms using a cryptographic check…

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…