CSA Z10083 : 2008
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by
OXYGEN CONCENTRATOR SUPPLY SYSTEMS FOR USE WITH MEDICAL GAS PIPELINE SYSTEMS
Hardcopy , PDF
28-09-2017
English
01-01-2013
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
5 Sources of supply
6 Requirements for components
7 Monitoring and alarm systems
8 Marking
9 Installation
10 Testing, commissioning and certification
11 Information to be supplied by the manufacturer
12 Implementation of use of oxygen-enriched air
Annex A (informative) - Schematic representations of oxygen
concentrator supply systems
Annex B (informative) - General guidelines for location of
supply systems
Annex C (informative) - Guidelines for emergency procedures
Annex D (informative) - Procedure for testing and commissioning
Annex E (informative) - Typical forms for certification of
an oxygen concentrator supply system
Annex F (informative) - Recommended minimum requirements for
preventive maintenance
Annex G (informative) - Recommendations for installation
Annex H (informative) - Risk and risk management
Annex I (informative) - Recommendations for sizing and capacity
Annex J (informative) - Recommendations for filling cylinders
with oxygen-enriched air
Annex K (informative) - Rationale
Bibliography
Defines requirements for the design and installation of an oxygen concentrator supply system for use with a medical gas pipeline distribution system that complies with ISO 7396-1.
| DocumentType |
Standard
|
| Pages |
74
|
| ProductNote |
Reconfirmed EN
|
| PublisherName |
Canadian Standards Association
|
| Status |
Withdrawn
|
| SupersededBy |
| ISO/IEC 17025:2005 | General requirements for the competence of testing and calibration laboratories |
| Z7396.1-17 | Medical gas pipeline systems - Part 1: Pipelines for medical gases, medical vacuum, medical support gases, and anaesthetic gas scavenging systems |
| ISO 4126-1:2013 | Safety devices for protection against excessive pressure — Part 1: Safety valves |
| CSA B51 : 2014 | BOILER, PRESSURE VESSEL, AND PRESSURE PIPING CODE |
| CGA P 8.1 : 2016 | SAFE INSTALLATION AND OPERATION OF PSA AND MEMBRANE OXYGEN AND NITROGEN GENERATORS |
| ISO 8359:1996 | Oxygen concentrators for medical use Safety requirements |
| ISO 15001:2010 | Anaesthetic and respiratory equipment Compatibility with oxygen |
| ISO 21969:2009 | High-pressure flexible connections for use with medical gas systems |
| ISO 5145:2014 | Cylinder valve outlets for gases and gas mixtures Selection and dimensioning |
| ISO 32:1977 | Gas cylinders for medical use — Marking for identification of content |
| ISO 5359:2014 | Anaesthetic and respiratory equipment — Low-pressure hose assemblies for use with medical gases |
| ISO/TR 16142:2006 | Medical devices Guidance on the selection of standards in support of recognized essential principles of safety and performance of medical devices |
| ISO 3746:2010 | Acoustics Determination of sound power levels and sound energy levels of noise sources using sound pressure Survey method using an enveloping measurement surface over a reflecting plane |
| ISO 14644-1:2015 | Cleanrooms and associated controlled environments Part 1: Classification of air cleanliness by particle concentration |
| ISO 407:2004 | Small medical gas cylinders Pin-index yoke-type valve connections |
| ISO 14971:2007 | Medical devices Application of risk management to medical devices |
| ISO 4135:2001 | Anaesthetic and respiratory equipment Vocabulary |
| CSA Z305.6 : 1992 | MEDICAL OXYGEN CONCENTRATOR CENTRAL SUPPLY SYSTEM FOR USE WITH NONFLAMMABLE MEDICAL GAS PIPING SYSTEMS |
| ISO 10524-2:2005 | Pressure regulators for use with medical gases Part 2: Manifold and line pressure regulators |
| ISO 7396-1:2016 | Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases and vacuum |
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