ISO 16571:2014
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by
Systems for evacuation of plume generated by medical devices
Hardcopy , PDF
English
11-03-2014
09-04-2025
ISO 16571:2014 specifies requirements and guidelines for the design, manufacture, installation, function, performance, maintenance, servicing, documentation, testing, and commissioning of equipment for evacuation of plume generated by medical devices.
ISO 16571:2014 is applicable to
a) portable and mobile plume evacuation systems,
b) local stationary plume evacuation systems,
c) dedicated central pipeline systems for plume evacuation systems, and
d) plume evacuation systems integrated into other equipment (e.g. laser equipment).
| Committee |
ISO/TC 121/SC 6
|
| DevelopmentNote |
Supersedes ISO/DIS 16571. (03/2014)
|
| DocumentType |
Standard
|
| Pages |
36
|
| ProductNote |
THIS STANDARD ALSO REFERS TO IEC 60601-6-08
|
| PublisherName |
International Organization for Standardization
|
| Status |
Withdrawn
|
| SupersededBy | |
| UnderRevision |
| Standards | Relationship |
| NEN ISO 16571 : 2014 | Identical |
| BS ISO 16571:2014 | Identical |
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| NF EN ISO 11197 : 2016 | MEDICAL SUPPLY UNITS |
| EN ISO 11197:2016 | Medical supply units (ISO 11197:2016) |
| BS ISO 11197 : 2016 | MEDICAL SUPPLY UNITS |
| I.S. EN ISO 11197:2016 | MEDICAL SUPPLY UNITS (ISO 11197:2016) |
| UNE-EN ISO 11197:2016 | Medical supply units (ISO 11197:2016) |
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| IEC 60601-1:2005+AMD1:2012 CSV | Medical electrical equipment - Part 1: General requirements for basic safety and essential performance |
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| EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
| ISO 11197:2016 | Medical supply units |
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| 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 |
| C22.1HB-15 | Canadian Electrical Code Handbook - An Explanation of the Rules of the Canadian Electrical Code, Part I |
| 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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