EVS-EN ISO 10079-1:2009

Medical suction equipment - Part 1: Electrically powered suction equipment - Safety requirements

General information
Withdrawn from 05.01.2016
Base Documents
ISO 10079-1:1999; EN ISO 10079-1:2009
Directives or regulations
93/42/EEC Medical devices (MDD)

Although the standard’s status is withdrawn, it still has the presumption of conformity in the meaning of regulation 93/42/EEC and conformance with the regulation ’s requirements can be guaranteed by using the withdrawn version of the standard. The presumption of conformity is valid until a corresponding amendment is published in the Official Journal of the European Union.
To view the latest lists of harmonised standards published in the Official Journal of the European Union, visit:

Standard history
EVS-EN ISO 10079-1:1999
This part of ISO 10079 specifies minimum safety and performance requirements for medical and surgical suctionequipment (see Figure 1) for health care facilities such as hospitals, for domiciliary care of patients and for field andtransport use.Although such equipment may be driven by centrally powered piped vacuum systems, compressed gases andelectricity, or be manually powered for a variety of applications, this part of ISO 10079 addresses only mainselectricity- and battery-powered suction equipment.
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Standard monitoring
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