SIS-EN-ISO-10079-3 › Medical suction equipment - Part 3: Suction equipment powered from a vacuum or positive pressure gas source (ISO 10079-3:2014)
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This part of ISO 10079 specifies safety and performance requirements for medical suction equipment powered from a vacuum or pressure source (see Figure 1). In particular it applies to connections for pipelines and Venturi attachments. Suction equipment with components controlled by electrical means, e.g. electronic timing, may also need to comply with IEC 60601-1.
To find similar documents by classification:
11.040.10 (Anaesthetic, respiratory and reanimation equipment Including medical gas installations)
Medical devices. Directive 2007/47/EC of the European Parliament and of the council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market
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Designation Name
SS-EN ISO 10079-3:2014
Revision Level
2014 EDITION
Status
Current
Publication Date
May 22, 2014
Language(s)
English
Page Count
48
International Equivalent
EN ISO 10079-3:2014(IDT); ISO 10079-3:2014(IDT)