UNE-EN ISO 7396-1:2016
Current
The latest, up-to-date edition.
Medical gas pipeline systems - Part 1: Pipeline systems for compressed medical gases and vacuum (ISO 7396-1:2016)
Hardcopy , PDF
02-11-2016
1.1 This part of ISO 7396 specifies requirements for design, installation, function, performance, testing,
commissioning and documentation of pipeline systems used in healthcare facilities for the following:
- oxygen;
- nitrous oxide;
- medical air;
- carbon dioxide;
- oxygen/nitrous oxide mixtures (see Note 1);
- helium/oxygen mixtures;
- (*) oxygen 93;
- gases and gas mixtures classified as medical device, gases delivered to medical devices
or intended for medical purposes or gases and gas mixtures for medicinal use not
specified above;
- air for driving surgical tools;
- nitrogen for driving surgical tools;
- vacuum.
NOTE 1: Regional or national regulations can prohibit the distribution of oxygen/nitrous oxide mixtures in
medical gas pipeline systems.
NOTE 2: Anesthetic gas scavenging disposal systems are covered in ISO 7396-2.
This part of ISO 7396 includes requirements for supply systems, pipeline distribution systems, control
systems, monitoring and alarm systems and non-interchangeability between components of different
gas/vacuum systems.
This part of ISO 7396 specifies safety requirements for pipeline systems used in health care facilities, both
public and private. It applies to all facilities providing health care services regardless of type, size, location, or
range of services, including, but not limited to:
(a) acute care healthcare facilities;
(b) internal patient continuing care healthcare facilities;
(c) long-term care facilities;
(d) community-based providers;
(e) ambulatory and external patient care clinics (e.g. day surgery, endoscopy clinics and doctors offices).
NOTE: This part of ISO 7396 can also be used as reference for pipeline systems for medical gases and
vacuum intended to be installed in places other than healthcare facilities.
1.2 This part of ISO 7396 applies to the following different types of oxygen supply systems:
- supply systems in which all sources of supply deliver oxygen; in this case the concentration of the gas will be
>99%;
- supply systems in which all sources of supply deliver oxygen 93; in this case the concentration of the gas
may vary between 90% and 96%;
NOTE: In some countries, a mixture of oxygen 93 and oxygen can be delivered by a medical gas supply
system. In this case the concentration of the gas can vary between 90% and >99%.
1.3 This part of ISO 7396 also applies to:
- extensions of existing pipeline distribution systems;
- modifications of existing pipeline distribution systems;
- modifications or replacement of supply systems or sources of supply.
1.4 Oxygen concentrators for domiciliary use are excluded from the scope of this standard.
NOTE Requirements for oxygen concentrators for domiciliary use are specified in ISO 80601-2-69.
1.5 (*) EN 14931 defines additional requirements for hyperbaric application, in particular for flows and
pressures of compressed air required to pressurize the hyperbaric chamber and to drive other connected
services. Also included are requirements for oxygen and other treatment gases administered to patients.
1.6 This part of ISO 7396 does not apply to vacuum systems intended to be used in dentistry.
1.7 This part of ISO 7396 does not apply to filling systems for transportable cylinders and transportable
cylinder bundle systems above 30 bar(g).
| Committee |
CTN 110
|
| DevelopmentNote |
Supersedes UNE EN 737-3. (05/2009) Supersedes UNE 110013. (12/2013) NEW CHILD AMD 1 2019 IS ADDED
|
| DocumentType |
Standard
|
| Pages |
194
|
| ProductNote |
NEW CHILD AMD 1 2019 IS ADDED.
|
| PublisherName |
Asociación Española de Normalización
|
| Status |
Current
|
| Standards | Relationship |
| NF EN ISO 7396-1 : 2016 | Identical |
| ISO 7396-1:2016 | Identical |
| NEN EN ISO 7396-1 : 2016 | Identical |
| NS EN ISO 7396-1 : 2016 | Identical |
| NBN EN ISO 7396-1 : 2016 | Identical |
| I.S. EN ISO 7396-1:2016 | Identical |
| EN ISO 7396-1:2016 | Identical |
| BS EN ISO 7396-1:2016 | Identical |
| DIN EN ISO 7396-1:2016-09 | Identical |
| ISO 7183:2007 | Compressed-air dryers — Specifications and testing |
| ISO 17672:2016 | Brazing — Filler metals |
| ISO 8573-5:2001 | Compressed air — Part 5: Test methods for oil vapour and organic solvent content |
| ISO 80601-2-69:2014 | Medical electrical equipment — Part 2-69: Particular requirements for basic safety and essential performance of oxygen concentrator equipment |
| ISO 11114-1:2012 | Gas cylinders — Compatibility of cylinder and valve materials with gas contents — Part 1: Metallic materials |
| EN 12021:2014 | Respiratory equipment - Compressed gases for breathing apparatus |
| ISO 4126-1:2013 | Safety devices for protection against excessive pressure — Part 1: Safety valves |
| CGA P 8.1 : 2016 | SAFE INSTALLATION AND OPERATION OF PSA AND MEMBRANE OXYGEN AND NITROGEN GENERATORS |
| ISO 10524-4:2008 | Pressure regulators for use with medical gases — Part 4: Low-pressure regulators |
| EN 1254-1:1998 | Copper and copper alloys - Plumbing fittings - Part 1: Fittings with ends for capillary soldering or capillary brazing to copper tubes |
| EN 475 : 1995 | MEDICAL DEVICES - ELECTRICALLY GENERATED ALARM SIGNALS |
| ISO 8359:1996 | Oxygen concentrators for medical use — Safety requirements |
| ISO 15001:2010 | Anaesthetic and respiratory equipment — Compatibility with oxygen |
| ISO 13485:2016 | Medical devices — Quality management systems — Requirements for regulatory purposes |
| ISO 8573-8:2004 | Compressed air — Part 8: Test methods for solid particle content by mass concentration |
| ISO 8573-2:2007 | Compressed air — Part 2: Test methods for oil aerosol content |
| ISO 10083:2006 | Oxygen concentrator supply systems for use with medical gas pipeline systems |
| IEC 60601-1-8:2006+AMD1:2012 CSV | Medical electrical equipment - Part 1-8: General requirements forbasic safety and essential performance - Collateral Standard: General requirements, tests and guidance for alarm systems inmedical electrical equipment and medical electrical systems |
| ISO 7396-2:2007 | Medical gas pipeline systems — Part 2: Anaesthetic gas scavenging disposal systems |
| 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 |
| IEC 60601-1-2:2014 | Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests |
| CGA E 10 : 2013 | MAINTENANCE OF MEDICAL GAS AND VACUUM SYSTEMS IN HEALTH CARE FACILITIES |
| ISO 8573-1:2010 | Compressed air — Part 1: Contaminants and purity classes |
| ISO 5359:2014 | Anaesthetic and respiratory equipment — Low-pressure hose assemblies for use with medical gases |
| ISO 8573-3:1999 | Compressed air — Part 3: Test methods for measurement of humidity |
| EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
| 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 11197:2016 | Medical supply units |
| ISO 11114-2:2013 | Gas cylinders — Compatibility of cylinder and valve materials with gas contents — Part 2: Non-metallic materials |
| EN 15908:2010 | Anaesthetic and respiratory equipment - Non-interchangeable screw-threaded (NIST) low-pressure connectors for medical gases |
| ISO 13585:2012 | Brazing — Qualification test of brazers and brazing operators |
| NFPA 99 : 2018 | HEALTH CARE FACILITIES CODE |
| FD S90 155 : 2016 FD | PIPELINE FOR COMPRESSED MEDICAL GASES AND VACUUM - ADDITIONAL ELEMENTS FOR DESIGN AND DELIVERY ACCEPTANCE |
| ISO 14644-1:2015 | Cleanrooms and associated controlled environments — Part 1: Classification of air cleanliness by particle concentration |
| ISO 9001:2015 | Quality management systems — Requirements |
| ISO 29463-1:2017 | High efficiency filters and filter media for removing particles from air — Part 1: Classification, performance, testing and marking |
| EN 14931:2006 | Pressure vessels for human occupancy (PVHO) - Multi-place pressure chamber systems for hyperbaric therapy - Performance, safety requirements and testing |
| ISO 407:2004 | Small medical gas cylinders — Pin-index yoke-type valve connections |
| EN 13134:2000 | Brazing - Procedure approval |
| ISO 8573-6:2003 | Compressed air — Part 6: Test methods for gaseous contaminant content |
| AS 2896-2011 | Medical gas systems - Installation and testing of non-flammable medical gas pipeline systems |
| ISO/TR 7470:1988 | Valve outlets for gas cylinders — List of provisions which are either standardized or in use |
| ISO 9170-1:2017 | Terminal units for medical gas pipeline systems — Part 1: Terminal units for use with compressed medical gases and vacuum |
| ISO 14971:2007 | Medical devices — Application of risk management to medical devices |
| EN 13348:2016 | Copper and copper alloys - Seamless, round copper tubes for medical gases or vacuum |
| ISO 4135:2001 | Anaesthetic and respiratory equipment — Vocabulary |
| ISO 8573-4:2001 | Compressed air — Part 4: Test methods for solid particle content |
| ISO 18082:2014 | Anaesthetic and respiratory equipment — Dimensions of non-interchangeable screw-threaded (NIST) low-pressure connectors for medical gases |
| 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 |
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