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SRPS EN ISO 10079-2:2017

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

Dec 25, 2017
95.99   Withdrawal of Standard   Oct 31, 2022

General information

95.99     Oct 31, 2022

ISS

Z076

European Norm

11.040.10  

English  

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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 directives

NOTE: If the word "harmonized" (marked in green) is not found in the field with the name of the directive, it means that the European standard is not cited in the OJEU.

93/42/EEC

Medical devices

Directive 93/42/EEC
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

Directive 2007/47/EC

Life cycle

PREVIOUSLY

WITHDRAWN
SRPS EN ISO 10079-2:2011

NOW

WITHDRAWN
SRPS EN ISO 10079-2:2017
95.99 Withdrawal of Standard
Oct 31, 2022

REVISED BY

PUBLISHED
SRPS EN ISO 10079-2:2022

Related project

Adopted from EN ISO 10079-2:2014

Adopted from ISO 10079-2:2014 IDENTICAL