General Information

Abstract

2019-02-19 - JO - TC decision 17/2018  (BT N 11332 - BT C160/2018)  to remove this work item from the harmonisation process linked with the MDD (93/42/EEC) thereby removing the need for annex ZA and allowing the standard to be publish without change as EN ISO.
2012-06-26 ST - Annex Z deemed as acceptable for the EC by the Consultant
MINOR AMENDMENT      MINOR AMENDMENT       MINOR AMENDMENT       MINOR AMENDMENT

Status
Withdrawn
Publication Date
14-Dec-2011
Withdrawal Date
22-Sep-2026
Current Stage
9960 - Withdrawal effective - Withdrawal
Start Date
15-Oct-2014
Completion Date
23-Sep-2026
Directive
Not Harmonized93/42/EEC - Medical devices
OJ Ref: C, C 262 OJ Date: 30-Aug-2012

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Amendment

EN ISO 5359:2008/A1:2012

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Effective Date
05-Sep-2012
Effective Date
28-Jan-2026
Effective Date
28-Jan-2026
Effective Date
12-Feb-2026
Effective Date
08-Jun-2022

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Amendment

EN ISO 5359:2008/A1:2012

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Frequently Asked Questions

EN ISO 5359:2008/A1:2011 is a amendment published by the European Committee for Standardization (CEN). Its full title is "Low-pressure hose assemblies for use with medical gases - Amendment 1 (ISO 5359:2008/Amd 1:2011)". This standard covers: 2019-02-19 - JO - TC decision 17/2018 (BT N 11332 - BT C160/2018) to remove this work item from the harmonisation process linked with the MDD (93/42/EEC) thereby removing the need for annex ZA and allowing the standard to be publish without change as EN ISO. 2012-06-26 ST - Annex Z deemed as acceptable for the EC by the Consultant MINOR AMENDMENT MINOR AMENDMENT MINOR AMENDMENT MINOR AMENDMENT

2019-02-19 - JO - TC decision 17/2018 (BT N 11332 - BT C160/2018) to remove this work item from the harmonisation process linked with the MDD (93/42/EEC) thereby removing the need for annex ZA and allowing the standard to be publish without change as EN ISO. 2012-06-26 ST - Annex Z deemed as acceptable for the EC by the Consultant MINOR AMENDMENT MINOR AMENDMENT MINOR AMENDMENT MINOR AMENDMENT

EN ISO 5359:2008/A1:2011 is classified under the following ICS (International Classification for Standards) categories: 11.040.10 - Anaesthetic, respiratory and reanimation equipment; 83.140.40 - Hoses. The ICS classification helps identify the subject area and facilitates finding related standards.

EN ISO 5359:2008/A1:2011 has the following relationships with other standards: It is inter standard links to EN ISO 5359:2014, EN 12514:2020, EN ISO 23553-1:2014, ISO 5359:2008/Amd 1:2011, EN ISO 5359:2008. Understanding these relationships helps ensure you are using the most current and applicable version of the standard.

EN ISO 5359:2008/A1:2011 is associated with the following European legislation: EU Directives/Regulations: 93/42/EEC; Standardization Mandates: M/023. When a standard is cited in the Official Journal of the European Union, products manufactured in conformity with it benefit from a presumption of conformity with the essential requirements of the corresponding EU directive or regulation.

EN ISO 5359:2008/A1:2011 is available in PDF format for immediate download after purchase. The document can be added to your cart and obtained through the secure checkout process. Digital delivery ensures instant access to the complete standard document.

Standards Content (Sample)


SLOVENSKI STANDARD
01-marec-2012
1L]NRWODþQHSRYH]RYDOQHFHYL]DGHOR]PHGLFLQVNLPLSOLQL'RSROQLOR$ ,62
$PG
Low-pressure hose assemblies for use with medical gases - Amendment 1 (ISO
5359:2008/Amd 1:2011)
Niederdruck-Schlauchleitungssysteme zur Verwendung mit medizinischen Gasen (ISO
5359:2008/Amd 1:2011)
Flexibles de raccordement à basse pression pour utilisation avec les gaz médicaux -
Amendement 1 (ISO 5359:2008/Amd 1:2011)
Ta slovenski standard je istoveten z: EN ISO 5359:2008/A1:2011
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
83.140.40 Gumene cevi Hoses
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

EUROPEAN STANDARD
EN ISO 5359:2008/A1
NORME EUROPÉENNE
EUROPÄISCHE NORM
December 2011
ICS 83.140.40; 11.040.10
English Version
Low-pressure hose assemblies for use with medical gases -
Amendment 1 (ISO 5359:2008/Amd 1:2011)
Flexibles de raccordement à basse pression pour utilisation Niederdruck-Schlauchleitungssysteme zur Verwendung mit
avec les gaz médicaux - Amendement 1 (ISO medizinischen Gasen - Änderung 1 (ISO 5359:2008/Amd
5359:2008/Amd 1:2011) 1:2011)
This amendment A1 modifies the European Standard EN ISO 5359:2008; it was approved by CEN on 14 December 2011.

CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for inclusion of this
amendment into the relevant national standard without any alteration. Up-to-date lists and bibliographical references concerning such
national standards may be obtained on application to the CEN-CENELEC Management Centre or to any CEN member.

This amendment exists in three official versions (English, French, German). A version in any other language made by translation under the
responsibility of a CEN member into its own language and notified to the CEN-CENELEC Management Centre has the same status as the
official versions.
CEN members are the national standards bodies of Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech Republic, Denmark, Estonia,
Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland,
Portugal, Romania, Slovakia, Slovenia, Spain, Sweden, Switzerland and United Kingdom.

EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2011 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 5359:2008/A1:2011: E
worldwide for CEN national Members.

Contents Page
Foreword .3
Annex ZA (informative) Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC .4

Foreword
This document (EN ISO 5359:2008/A1:2011) has been prepared by Technical Committee ISO/TC 121
"Anaesthetic and respiratory equipment" in collaboration with Technical Committee CEN/TC 215 “Respiratory
and anaesthetic equipment” the secretariat of which is held by BSI.
This European Standard shall be given the status of a national standard, either by publication of an identical
text or by endorsement, at the latest by June 2012, and conflicting national standards shall be withdrawn at
the latest by June 2012.
Attention is drawn to the possibility that some of the elements of this document may be the subject of patent
rights. CEN [and/or CENELEC] shall not be held responsible for identifying any or all such patent rights.
This document has been prepared under a mandate given to CEN by the European Commission and the
European Free Trade Association, and supports essential requirements of EU Directive.
For relationship with EU Directive, see informative Annex ZA, which is an integral part of this document.
According to the CEN/CENELEC Internal Regulations, the national standards organizations of the following
countries are bound to implement this European Standard: Austria, Belgium, Bulgaria, Croatia, Cyprus, Czech
Republic, Denmark, Estonia, Finland, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia,
Lithuania, Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Slovakia, Slovenia, Spain,
Sweden, Switzerland and the United Kingdom.
Endorsement notice
The text of ISO 5359:2008/Amd 1:2011 has been approved by CEN as a EN ISO 5359:2008/A1:2011 without
any modification.
EN ISO 5359:20
...