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SRPS EN ISO 5360:2013

Anaesthetic vaporizers - Agent-specific filling systems (ISO 5360:2012)

Sep 23, 2013
95.99   Withdrawal of Standard   Sep 25, 2017

General information

95.99     Sep 25, 2017

ISS

Z076

European Norm

11.040.10  

English  

from plan 2013

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Scope

ISO 5360:2012 specifies requirements, including dimensions, for agent-specific filling systems for agent-specific anaesthetic vaporizers.
ISO 5360:2012 does not specify construction materials. Because of the unique properties of desflurane, dimensions for this agent have not been specified in ISO 5360:2012.

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

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WITHDRAWN
SRPS EN ISO 5360:2011

NOW

WITHDRAWN
SRPS EN ISO 5360:2013
95.99 Withdrawal of Standard
Sep 25, 2017

REVISED BY

PUBLISHED
SRPS EN ISO 5360:2017

Related project

Adopted from EN ISO 5360:2012

Adopted from ISO 5360:2012 IDENTICAL