Information technology - Data communication - 15-pole DTE/DCE interface
connector and contact number...
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…
Safety of household and similar electrical appliances - Part 2: Particular
requirements for toaster...
This National Standard of Canada is based on International Standard CEI/IEC 335-2-9:1993.
1. Scope
This clause of part 1 is replaced by:
This standard deals with the safety of portable electric appliances having a
cooking function such as baking, roasting and grilling, intended for household
purposes, their rated voltage being not more that 250 V.
Note 1 - Examples of appliances…
Safety of household and similar electrical appliances - Part 2: Particular requirements for commerci...
1. Scope
This clause of Part 1 is applicable except as follows:
1.1 Replacement:
This standard applies to the following electrically operated commercial appliances, not intended for household use:
- grillers, including rotary or continuous types;
- toasters, including rotary or continuous types;
- similar appliances for grilling by…
Safety requirements for electrical equipment for measurement, control, and laboratory use - Part 2-0...
This National Standard of Canada is based on International Standard IEC 1010-2-020:1992.
1. Scope and Object
This clause of Part 1 is applicable except as follows:
1.1 Scope
This Particular Standard specifies requirements for the safety of electrically powered laboratory centrifuges designed to be installed and used in accordance with the Rules of the Canadian Electr ical Code,…
Anaesthetic vaporizers - Agent-specific filling systems
This National Standard of Canada is based on International Standard ISO 5360:1993.
1 Scope
This International Standard specifies the dimensions of agent-specific filling
systems for agent-specific anaesthetic vaporizers.
This International Standard does not specify construction materials. Materials
used for the parts of filling systems which come into contact with liquid
anaesthetic…
This is a searchable PDF.
Scope
1.1 Applicability This standard applies to the installation of a conversion burner with an input of 400,000 Btu per hour (117 228 W) or less and design certified as complying with the Standard for Domestic Gas Conversion Burners, ANSI Z21.17. This standard, in conjunction with local codes or, in the absence of local codes, with the National Fuel Gas Code,…
This National Standard of Canada is equivalent to American National Standards
Institute standard ANSI T1.408-1990.
1.1 General
It establishes performance and technical criteria for interfacing and
interconnecting the various functional groups shown in figure 1. Compliance
with this standard is intended to ensure compatibility at the interface points
/a and /b (figure 1) and should not…
This Guide establishes basic safety principles for technical bodies preparing national and international standards for products which are intended specifically for use by children; these principles should also apply to products with which children are likely to come into contact. The following aspects are considered: ergonomic considerations, toxicity, flammability and thermal injuries, ingestion…
This Guide establishes basic safety principles for technical bodies preparing national and international standards for products which are intended specifically for use by children; these principles should also apply to products with which children are likely to come into contact. The following aspects are considered: ergonomic considerations, toxicity, flammability and thermal injuries, ingestion…
Clinical investigation of medical devices for human subjects — Good clinical practice
This document addresses good clinical practice for the design, conduct, recording and reporting of clinical investigations carried out in human subjects to assess the clinical performance or effectiveness and safety of medical devices.
For post-market clinical investigations, the principles set forth in this document are intended to be followed as far as relevant, considering the nature of the…