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EVS-EN ISO 10079-2:2014

Medical suction equipment - Part 2: Manually powered suction equipment (ISO 10079-2:2014)

General information

Withdrawn from 01.06.2022
Base Documents
ISO 10079-2:2014; EN ISO 10079-2:2014
Directives or regulations
None

Standard history

Status
Date
Type
Name
01.06.2022
Main
05.06.2014
Main
07.08.2009
Main
EVS-EN ISO 10079-2:2009
This part of ISO 10079 specifies safety and performance requirements for manually powered medical suction equipment intended for oro-pharyngeal suction. It covers equipment operated by foot or by hand or both (see Figure 1). The commonest use of manually powered suction is in situations outside of health care settings often described as field or transport use. Use in these situations may involve extreme conditions of weather or terrain and therefore this standard calls for additional requirements for suction equipment intended for field or transport use. Non-electrical suction equipment which may be integrated with electrical equipment is included in the scope of this part of ISO 10079. This part of ISO 10079 does not apply to electrically powered suction equipment, whether mains electricity- or battery-powered, which is dealt with in ISO 10079-1, nor to suction equipment powered from a vacuum or positive pressure source which is dealt with in ISO 10079-3, nor to the following: a) central power supply (by vacuum/compressed air generation), piping systems of vehicles and buildings, and wall connectors; b) cathether tubes, drains, curettes and suction tips; c) syringes; d) dental suction equipment; e) waste gas scavenging systems; f) laboratory suction; g) autotransfusion systems; h) passive urinary drainage; i) closed systems for wound drainage; j) gravity gastric drainage; k) orally operated mucous extractors; l) suction equipment where the collection container is downstream of the vacuum pump; m) equipment marked as suction unit for permanent tracheostomy; n) ventouse (obstetric) equipment;

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