EN ISO 10079-2:2014

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

Publication date:   Jul 17, 2014

General information

99.60 Withdrawal effective   May 25, 2022

CEN

CEN/TC 215 Respiratory and anaesthetic equipment

European Norm

11.040.10   Anaesthetic, respiratory and reanimation equipment

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Scope

ISO 10079-2:2014 specifies safety and performance requirements for medical, manually powered suction equipment intended for oro-pharyngeal suction. It covers equipment operated by foot or by hand or both. Annex C illustrates the three parts of ISO 10079 by providing a schematic for typical systems.
ISO 10079-2:2014 has additional requirements for suction equipment intended for field use or transport use.

Related legislation

Legislation related to this standard

93/42/EEC

Medical devices

2007/47/EC

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

Life cycle

PREVIOUSLY

WITHDRAWN
EN ISO 10079-2:2009

NOW

WITHDRAWN
EN ISO 10079-2:2014
99.60 Withdrawal effective
May 25, 2022

REVISED BY

PUBLISHED
EN ISO 10079-2:2022