METALLIC UNDERGROUND PIPING FOR FLAMMABLE AND COMBUSTIBLE LIQUIDS
1.1 This Standard sets forth the minimum requirements for metallic and composite primary carrier,
secondary containment, normal vent and vapour recovery and integral primary/secondary pipe systems
(pipe and fittings) intended for underground use in distribution and venting applications of
petroleum-based flammable liquids and combustible liquids, alcohols, and alcohol-blended fuels as…
Safety of Household and Similar Appliances — Part 1: General Requirements
1 Scope
This International Standard deals with the safety of electrical appliances for household and similar
purposes, their RATED VOLTAGE being not more than 250 V for single-phase appliances and 480 V for other
appliances.
Appliances not intended for normal household use but which nevertheless may be a source of danger to
the public, such as appliances intended to be used by laymen in shops,…
Fibre-cement corrugated sheets and fittings for roofing and cladding
ISO 10904:2011 specifies technical requirements and methods for the inspection and testing of straight short and long fibre-cement profiled sheets and their fibre-cement fittings designed to provide the weather-exposed surfaces on roofs and internal and external walls of buildings.
Products covered by ISO 10904:2011 can be used for other purposes, provided they comply with the appropriate…
Medical electrical equipment — Part 2-54: Particular requirements for the basic safety and essential...
This National Standard of Canada is equivalent to International Standard IEC 60601-2-54:2009.
201.1.1 Scope
Replacement:
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of
ME EQUIPMENT and ME SYSTEMS intended to be used for projection RADIOGRAPHY and
RADIOSCOPY. IEC 60601-2-43 applies to ME EQUIPMENT and ME SYSTEMS intended to be used
for…
Medical electrical equipment — Part 2-5: Particular requirements for the basic safety and essential ...
This National Standard of Canada is equivalent to International Standard IEC 60601-2-5:2009.
201.1.1 Scope
Replacement:
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of
ULTRASONIC PHYSIOTHERAPY EQUIPMENT as defined in 201.3.216, hereafter referred to as
ME EQUIPMENT.
This standard only relates to ULTRASONIC PHYSIOTHERAPY EQUIPMENT employing a…
Medical electrical equipment — Part 2-41: Particular requirements for the basic safety and essential...
This National Standard of Canada is equivalent to International Standard IEC 60601-2-41:2009.
201.1.1 *Scope
Replacement:
This particular standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of SURGICAL
LUMINAIRES AND LUMINAIRES FOR DIAGNOSIS, hereafter referred to as ME EQUIPMENT.
This particular standard does not apply to
– headlights;
– endoscopes, laparoscopes and…
Medical electrical equipment — Part 2-18: Particular requirements for the basic safety and essential...
This National Standard of Canada is equivalent to International Standard IEC 60601-2-18:2009.
Clause 1 of the general standard1) applies, except as follows:
201.1.1 * Scope
Replacement:
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of
ENDOSCOPIC EQUIPMENT together with its INTERCONNECTION CONDITIONS and INTERFACE
CONDITIONS.
The general…
Medical electrical equipment — Part 1-11: General requirements for basic safety and essential perfor...
This National Standard of Canada is equivalent to International Standard IEC 60601-1-11:2010.
1.1 * Scope
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of
MEDICAL ELECTRICAL EQUIPMENT and MEDICAL ELECTRICAL SYSTEMS, hereafter referred to as
ME EQUIPMENT and ME SYSTEMS, which are intended by their MANUFACTURER for use in the
HOME HEALTHCARE ENVIRONMENT, as…
Medical electrical equipment — Part 2-52: Particular requirements for the basic safety and essential...
This National Standard of Canada is equivalent to International Standard IEC 60601-2-52:2009.
201.1.1 * Scope
Replacement:
This International Standard applies to the BASIC SAFETY and ESSENTIAL PERFORMANCE of
MEDICAL BEDS intended for adults, hereafter referred to as MEDICAL BED as defined in
201.3.212.
If a clause or subclause is specifically intended to be applicable to a MEDICAL BED only,…
Cardiovascular implants and extracorporeal systems — Vascular device-drug combination products
ISO/TS 12417:2011 specifies requirements for vascular device-drug combination products (VDDCPs) based upon current technical and medical knowledge. VDDCPs are medical devices with various clinical indications for use in the human vascular blood system. A VDDCP incorporates, as an integral part, substance(s) which, if used separately, can be considered to be a medicinal product (drug product) but…
