1 Scope
1.1
This Standard specifies the chassis and body requirements and required safety equipment for school buses.
1.2
This Standard applies to Types A1, A2, B, C, and D school buses.
1.3
This Standard does not cover after-market and retrofit installations. These installations are covered by federal and provincial regulations, and it is the responsibility of the appropriate…
Part 1
1 Scope
1.1
Except as indicated in Clause 1.2, Part 1 of this Standard applies to all boilers, pressure vessels, pressure piping, and fittings, as provided for by the Act (as defined in Clause 3) and identified in Part 1 of this Standard.
Notes:
1) In certain provinces there may be variations in the size limitations specified in Part 1 of this Standard. The regulatory…
Miniature Fuses - Part 6: Fuse-Holders for Miniature Cartridge Fuse-Links
This National Standard of Canada is based on International Standard CEI/IEC 127-6:1994, first edition, 1994-04, including Amendment 1:1996.
1.Scope and Object
1.1
This part of IEC 127 is applicable to fuse-holders for miniature cartridge fuse-links according to IEC 127-2 and sub-miniature fuse-links according to IEC 127-3 for the protection of electric appliances, electronic equipment and…
METHOD OF TEST FOR SURFACE BURNING CHARACTERISTICS
OF BUILDING MATERIALS AND ASSEMBLIES
1. SCOPE
1.1 This method of test for surface burning characteristics of building materials is
applicable to any type of building material that, by its own structural qualities or the manner in
which it is applied, is capable of supporting itself in position or may be supported in the test
furnace to a thickness comparable to its recommended use.
NOTE: For materials which cannot be so…
Paints, varnishes and plastics — Determination of non-volatile-matter content
ISO 3251:2003 specifies a method for determining the non-volatile-matter content by mass of paints, varnishes, binders for paints and varnishes, polymer dispersions and condensation resins such as phenolic resins (resols, novolak solutions, etc.).
The method is also applicable to formulated dispersions containing fillers, pigments and other auxiliaries (e.g. thickeners and film-forming agents).…
Packaging for terminally sterilized medical devices
This International Standard specifies the requirements for single-use materials and reusable containers used for packaging of terminally sterilized medical devices, whether produced industrially or in health care facilities.
This International Standard outlines principal requirements for packaging process development and validation for the manufacturer of terminally sterilized medical devices.…
1. Scope
1.1
This Standard specifies
(a) general design requirements;
(b) product marking and labelling;
(c) test procedures; and
(d) performance requirements
for single-occupancy mobility aids that are intended to be transported in vehicles having a gross vehicle weight rating (GVWR) of less than 7000 kg (15 500 lb) and equipped to accommodate occupants who are seated in a mobility aid. See…
Industrial Robots and Robot Systems - General Safety Requirements
1 Scope
1.1 Scope
This safety Standard applies to the manufacture, remanufacture, rebuild, installation, safeguarding, maintenance and repair, testing and start-up, and personnel training requirements for industrial robots and robot systems.
1.2 Purpose
The purpose of this Standard is to provide requirements for industrial robot manufacture, remanufacture, and rebuild; robot system integration/…
1 Scope
1.1
This Standard addresses issues related to the safety of human tissues used for transplantation purposes. It includes aspects of safety for potential and actual donors and recipients, personnel, and others who may be exposed to, or affected by, the transplant of tissues.
1.2
This Standard applies to establishments (or facilities) and individuals involved in the donor suitability…
1 Scope
1.1
This Standard addresses issues related to the safety of human cells of lymphohematopoietic origin used for transplantation purposes. It includes aspects of safety for potential and actual donors and recipients, personnel, and others who may be exposed to or affected by the transplant of lymphohematopoietic cells.
1.2
This Standard applies to establishments (or facilities)…