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.
This Standard was reviewed for Canadian adoption by the CSA Technical Committee on Perioperative Safety, under the jurisdiction of the CSA Strategic Steering Committee on Health Care Technology & Systems, and has been formally approved by the Technical Committee.
This Standard has been developed in compliance with Standards Council of Canada requirements for National Standards of Canada. It has been published as a National Standard of Canada by CSA Group.
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.