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EN ISO 5359:2014/A1:2017

(Amendment)

Anaesthetic and respiratory equipment - Low-pressure hose assemblies for use with medical gases - Amendment 1 (ISO 5359:2014/Amd 1:2017)

Anaesthetic and respiratory equipment - Low-pressure hose assemblies for use with medical gases - Amendment 1 (ISO 5359:2014/Amd 1:2017)

2017-08-31 - BTC 110/2017 - BT approve publication of EN ISO with modified Annex ZA & Foreword
2017-08-08 - Cannot allocate for publication due to negative assessment from Consultant.
CEN/BT C082/2011:  DOW = DAV + 36 months

Anästhesie- und Beatmungsgeräte - Niederdruck-Schlauchleitungssysteme zur Verwendung mit medizinischen Gasen - Änderung 1 (ISO 5359:2014/Amd 1:2017)

Matériel d'anesthésie et de réanimation respiratoire - Flexibles de raccordement à basse pression pour utilisation avec les gaz médicaux - Amendement 1 (ISO 5359:2014/Amd 1:2017)

Anestezijska in dihalna oprema - Nizkotlačne povezovalne cevi za delo z medicinskimi plini - Dopolnilo A1 (ISO 5359:2014/Amd 1:2017)

General Information

Status
Published
Publication Date
28-Nov-2017
Withdrawal Date
29-Nov-2020
ICS
11.040.10 - Anaesthetic, respiratory and reanimation equipment
83.140.40 - Hoses
Technical Committee
CEN/TC 215 - Respiratory and anaesthetic equipment
Drafting Committee
CEN/TC 215/WG 1 - Anaesthetic machines, medical breathing systems and anaesthetic gas scavenging systems
Current Stage
6060 - Definitive text made available (DAV) - Publishing
Start Date
29-Nov-2017
Completion Date
29-Nov-2017
Directive
93/42/EEC - Council Directive 93/42/EEC of 14 June 1993 concerning medical devices
Mandate
M/023 - Standardization mandate to CEN/CENELEC concerning the development of European standards relating to medical devices
Ref Project
SIST EN ISO 5359:2015/A1:2018 - Anaesthetic and respiratory equipment - Low-pressure hose assemblies for use with medical gases - Amendment 1 (ISO 5359:2014/Amd 1:2017)

Relations

Amends
EN ISO 5359:2014 - Anaesthetic and respiratory equipment - Low-pressure hose assemblies for use with medical gases (ISO 5359:2014)
Effective Date
25-Mar-2015

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EN ISO 5359:2015/A1:2018
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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 5359:2015/A1:2018
01-februar-2018
$QHVWH]LMVNDLQGLKDOQDRSUHPD1L]NRWODþQHSRYH]RYDOQHFHYL]DGHOR]
PHGLFLQVNLPLSOLQL'RSROQLOR$ ,62$PG
Anaesthetic and respiratory equipment - Low-pressure hose assemblies for use with
medical gases - Amendment 1 (ISO 5359:2014/Amd 1:2017)
Anästhesie- und Beatmungsgeräte - Niederdruck-Schlauchleitungssysteme zur
Verwendung mit medizinischen Gasen (ISO 5359:2014/Amd 1:2017)
Matériel d'anésthésie et de réanimation respiratoire - Flexibles de raccordement à basse
pression pour utilisation avec les gaz médicaux (ISO 5359:2014/Amd 1:2017)
Ta slovenski standard je istoveten z: EN ISO 5359:2014/A1:2017
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
83.140.40 Gumene cevi Hoses
SIST EN ISO 5359:2015/A1:2018 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

---------------------- Page: 1 ----------------------

SIST EN ISO 5359:2015/A1:2018

---------------------- Page: 2 ----------------------

SIST EN ISO 5359:2015/A1:2018


EN ISO 5359:2014/A1
EUROPEAN STANDARD

NORME EUROPÉENNE

November 2017
EUROPÄISCHE NORM
ICS 83.140.40; 11.040.10
English Version

Anaesthetic and respiratory equipment - Low-pressure
hose assemblies for use with medical gases - Amendment
1 (ISO 5359:2014/Amd 1:2017)
Matériel d'anesthésie et de réanimation respiratoire - Anästhesie- und Beatmungsgeräte - Niederdruck-
Flexibles de raccordement à basse pression pour Schlauchleitungssysteme zur Verwendung mit
utilisation avec les gaz médicaux - Amendement 1 (ISO medizinischen Gasen - Änderung 1 (ISO
5359:2014/Amd 1:2017) 5359:2014/Amd 1:2017)
This amendment A1 modifies the European Standard EN ISO 5359:2014; it was approved by CEN on 16 August 2017.

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, Former Yugoslav Republic of Macedonia, France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Latvia, Lithuania,
Luxembourg, Malta, Netherlands, Norway, Poland, Portugal, Romania, Serbia, Slovakia, Slovenia, Spain, Sweden, Switzerland,
Turkey and United Kingdom.





EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION

EUROPÄISCHES KOMITEE FÜR NORMUNG

CEN-CENELEC Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2017 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 5359:2014/A1:2017 E
worldwide for CEN national Members.

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SIST EN ISO 5359:2015/A1:2018
EN ISO 5359:2014/A1:2017 (E)
Contents Page
European foreword . 3
Annex ZA (informative) Relationship between this European Standard and the essential
requirements of Directive 93/42/EEC [OJ L 169] aimed to be covered . 5

2

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SIST EN ISO 5359:2015/A1:2018
EN ISO 5359:2014/A1:2017 (E)
European foreword
The text of this Amendment EN ISO 5359:2014/A1:2017 to the EN ISO 5359:2014 from Technical
Committee ISO/TC 121 “Anaesthetic and respiratory equipment” of the International Organization for
Standardization (ISO) has been taken over as an amendment to the European Standard by Technical
Committee CEN/TC 215 “Respiratory and anaesthetic equipment” the secretariat of which is held by
BSI.
This Amendment to the European Standard EN ISO 5359:2014 shall be given the status of a national
standard, either by publication of an identical text or by endorsement, at the latest by May 2018, and
conflicting national standards shall be withdrawn at the latest by November 2020.
Attention is drawn to the possibility that some of the elements of this document may be the subject of
patent rights. CEN 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 re
...

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