13/30242951 DC : 0
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
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BS ISO 16571 - MEDICAL GAS SYSTEMS - SYSTEMS FOR EVACUATION OF PLUME GENERATED BY MEDICAL DEVICES
Hardcopy , PDF
English
31-05-2014
Foreword
Introduction
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
5 Design requirements
6 Indicating systems
7 Plume extraction system pipeline
8 System components
9 Terminal units
10 Marking and colour coding
11 Pipeline installation
12 Testing, commissioning and certification of the
PES
13 Information to be supplied by the manufacturer
Annex A (informative) - Types of plume evacuation
systems
Annex B (informative) - Healthcare facility policies
and procedures
Annex C (informative) - Typical plume capture devices
and transfer tubings
Annex D (informative) - Bibliography
Annex E (informative) - Risk management checklist
Annex F (informative) - Operational management
Annex G (informative) - Rationale
Annex H (informative) - Example of procedure for testing
and commissioning for central systems
Annex I (informative) - Guidelines for flow-generating
devices consisting of fans or blowers
BS ISO 16571
| Committee |
CH/121/6
|
| DocumentType |
Draft
|
| Pages |
47
|
| PublisherName |
British Standards Institution
|
| Status |
Superseded
|
| SupersededBy |
| ISO 3744:2010 | Acoustics — Determination of sound power levels and sound energy levels of noise sources using sound pressure — Engineering methods for an essentially free field over a reflecting plane |
| IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
| ISO 15001:2010 | Anaesthetic and respiratory equipment — Compatibility with oxygen |
| ISO 5356-1:2015 | Anaesthetic and respiratory equipment — Conical connectors — Part 1: Cones and sockets |
| 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 |
| IEC 62366:2007+AMD1:2014 CSV | Medical devices - Application of usability engineering to medical devices |
| ISO 5359:2014 | Anaesthetic and respiratory equipment — Low-pressure hose assemblies for use with medical gases |
| EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
| ISO 11197:2016 | Medical supply units |
| IEC 60529:1989+AMD1:1999+AMD2:2013 CSV | Degrees of protection provided by enclosures (IP Code) |
| ANSI Z136.3 : 2011 | SAFE USE OF LASERS IN HEALTH CARE |
| NFPA 115 : 2016 | LASER FIRE PROTECTION |
| ISO 80369-1:2010 | Small-bore connectors for liquids and gases in healthcare applications — Part 1: General requirements |
| EN 1822-1:2009 | High efficiency air filters (EPA, HEPA and ULPA) - Part 1: Classification, performance testing, marking |
| 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 7396-1:2016 | Medical gas pipeline systems — Part 1: Pipeline systems for compressed medical gases and vacuum |
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