CAN/CSA-ISO 10079-1:16
Current
The latest, up-to-date edition.
Medical suction equipment - Part 1: Electrically powered suction equipment (Adopted ISO 10079-1:2015, third edition, 2015-11-01)
Hardcopy , PDF
01-01-2016
Foreword
1 Scope
2 Normative references
3 Terms and definitions
4 General requirements
5 Cleaning, disinfection and sterilization
6 Design requirements
7 Operational requirements
8 Physical requirements for suction equipment for
field use
9 Performance requirements for vacuum level and
flowrate
10 Resistance to environment of suction equipment
for field and/or transport use
11 Information to be supplied by the manufacturer
(labelling and instructions for use)
Annex A (normative) - Test methods
Annex B (informative) - Rationale statement
Annex C (informative) - Lumen size and its effect
on flowrate
Annex D (informative) - Schematic of suction
equipment
Bibliography
Defines safety and performance requirements for electrically powered medical and surgical suction equipment.
DevelopmentNote |
Supersedes CSA Z10079.1. (07/2016)
|
DocumentType |
Standard
|
ISBN |
978-1-4883-0640-2
|
Pages |
64
|
ProductNote |
NEW CHILD AMD 1 2019 IS NOW ADDED
|
PublisherName |
Canadian Standards Association
|
Status |
Current
|
Supersedes |
CSA Preface This is the second edition of CAN/CSA-ISO 10079-1, Medical suction equipment Part 1: Electrically powered suction equipment, which is an adoption without modification of the identically titled ISO (International Organization for Standardization) Standard 10079-1 (third edition, 2015-11-01). It supersedes the previous edition published in 2003 as CAN/CSA-Z10079-1 (adopted ISO 10079-1:1999). For brevity, this Standard will be referred to as "CAN/CSA-ISO 10079-1" throughout. Scope This part of ISO 10079 specifies safety and performance requirements for electrically powered medical and surgical suction equipment. It applies to equipment used in health care facilities such as hospitals, for domiciliary care of patients and for field and transport use. This part of ISO 10079 does not apply to the following: a) central power supply (by vacuum/compressed air generation), piping systems of vehicles and buildings, and wall connectors; b) end-pieces such as suction catheters, drains, curettes, Yankauer suckers and suction tips; c) syringes; d) dental suction equipment; e) anaesthetic gas scavenging systems; f) laboratory suction; g) autotransfusion systems; h) mucus extractors including neonatal mucus extractors; i) suction equipment where the collection container is downstream of the vacuum pump; j) ventouse (obstetric) equipment; k) suction equipment marked for endoscopic use only; l) plume evacuation systems.
Standards | Relationship |
ISO 10079-1:2015 | Identical |
ISO 8836:2014 | Suction catheters for use in the respiratory tract |
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 |
IEC 60601-1-6:2010+AMD1:2013 CSV | Medical electrical equipment - Part 1-6: General requirements for basic safety and essential performance - Collateral standard: Usability |
ISO 5356-1:2015 | Anaesthetic and respiratory equipment Conical connectors Part 1: Cones and sockets |
ISO 10651-4:2002 | Lung ventilators — Part 4: Particular requirements for operator-powered resuscitators |
IEC 62366:2007+AMD1:2014 CSV | Medical devices - Application of usability engineering to medical devices |
EN 1041:2008+A1:2013 | Information supplied by the manufacturer of medical devices |
IEC TR 60878:2015 | Graphical symbols for electrical equipment in medical practice |
ISO 10079-2:2014 | Medical suction equipment Part 2: Manually powered suction equipment |
IEC 60529:1989+AMD1:1999+AMD2:2013 CSV | Degrees of protection provided by enclosures (IP Code) |
ISO 10079-3:2014 | Medical suction equipment Part 3: Suction equipment powered from a vacuum or positive pressure gas source |
ISO 14155:2011 | Clinical investigation of medical devices for human subjects Good clinical practice |
ISO 14971:2007 | Medical devices Application of risk management to medical devices |
ISO 7000:2014 | Graphical symbols for use on equipment Registered symbols |
ISO 15223-1:2016 | Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements |
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