EN ISO 9170-1:2008

Terminal units for medical gas pipeline systems - Part 1: Terminal units for use with compressed medical gases and vacuum (ISO 9170-1:2008)

ISO 9170-1:2008 applies to:
terminal units intended for use in medical gas pipeline systems in accordance with ISO 7396-1, for use with the following medical gases:
oxygen,
nitrous oxide;
medical air;
carbon dioxide;
oxygen/nitrous oxide mixture [50 %/50 % (by volume)];
terminal units intended for use in medical gas pipeline systems in accordance with ISO 7396-1, for use with the following gases and services:
oxygen-enriched air;
air for driving surgical tools;
nitrogen for driving surgical tools;
vacuum.
It is intended especially to ensure the gas-specific assembly of terminal units and to prevent their interchange between different gases and services.
ISO 9170-1:2008 specifies requirements for terminal units for supply and disposal of nitrogen or air for driving surgical tools and requirements for probes intended to be connected to the gas-specific connection point which is part of the terminal unit.

Entnahmestellen für Rohrleitungssysteme für medizinische Gase - Teil 1: Entnahmestellen für medizinische Druckgase und Vakuum (ISO 9170-1:2008)

1.1   Dieser Teil von ISO 9170 gilt für
a)   Entnahmestellen, die in Rohrleitungssystemen für medizinische Gase nach ISO 7396 1 zur Verwendung mit den folgenden medizinischen Gasen vorgesehen sind:
   Sauerstoff;
   Distickstoffoxid (Lachgas);
   medizinische Luft;
   Kohlendioxid;
   Sauerstoff /Lachgasgemische [50 %/50 % (Volumenanteil)];
b)   Entnahmestellen, die in Rohrleitungssystemen für medizinische Gase nach ISO 7396 1 zur Verwendung mit den folgenden Gasen und Versorgungen vorgesehen sind:
   mit Sauerstoff angereicherte Luft;
   Luft zum Betreiben chirurgischer Werkzeuge;
   Stickstoff zum Betreiben chirurgischer Werkzeuge;
   Vakuum.
ANMERKUNG 1   Für Luft zum Betreiben chirurgischer Werkzeuge werden verschiedene Bezeichnungen und Symbole verwendet, wie zum Beispiel Luft für Instrumente, chirurgische Luft, Luftmotor, Air-700 und Air-800.
ANMERKUNG 2   Die Anforderungen in diesem Teil von ISO 9170 können als Anleitung für Entnahmestellen für sonstige Gase verwendet werden. Diese sonstigen Gase werden zur Aufnahme in diesen Teil von ISO 9170 berücksichtigt, wenn sie allgemein gebräuchlich werden.
Es ist vor allem beabsichtigt, die gasartspezifische Montage von Entnahmestellen sicherzustellen und zu verhindern, dass diese zwischen unterschiedlichen Gasen und Versorgungen vertauscht werden.
1.2   Dieser Teil von ISO 9170 legt Anforderungen an Entnahmestellen für die Bereitstellung und Entsorgung von Stickstoff oder Luft zum Betreiben chirurgischer Werkzeuge fest.
1.3   Dieser Teil von ISO 9170 legt Anforderungen an Stecker zum Anschluss an die gasartspezifische Verbindungsstelle fest, die Teil der Entnahmestelle ist.
1.4   Dieser Teil von ISO 9170 legt nicht die Maße von Steckern und von gasartspezifischen Verbindungs¬stellen der Entnahmestellen fest.
ANMERKUNG   Bestimmte regionale oder nationale Normen, die Maße von Steckern und gasartspezifischen Verbindungsstellen festlegen, sind in den Literaturhinweisen enthalten.

Prises murales pour systèmes de distribution de gaz médicaux - Partie 1: Prises murales pour les gaz médicaux comprimés et le vide (ISO 9170-1:2008)

L'ISO 9170-1:2008 est applicable aux
prises murales destinées à être utilisées dans les systèmes de distribution de gaz médicaux conformément à l'ISO 7396-1, conçus pour être utilisés avec les gaz médicaux suivants:
oxygène;
protoxyde d'azote;
air médical;
dioxyde de carbone;
mélanges d'oxygène et de protoxyde d'azote [50 %/50 % (fraction volumique)];
prises murales destinées à être utilisées dans les systèmes de distribution de gaz médicaux conformément à l'ISO 7396-1, conçus pour être utilisés avec les gaz et services suivants:
air enrichi en oxygène;
air moteur pour les instruments chirurgicaux;
azote moteur pour les instruments chirurgicaux;
vide.
Elle est notamment destinée à garantir le montage spécifique au gaz des prises murales et à en empêcher l'interchangeabilité entre les différents gaz.
L'ISO 9170-1:2008 spécifie les exigences relatives aux prises murales d'arrivée et d'évacuation d'azote ou d'air pour les instruments chirurgicaux, ainsi que les exigences relatives aux embouts destinés à être branchés au raccord spécifique au gaz faisant partie d'une prise murale.

Končni deli napeljav za medicinske pline - 1. del: Končni deli za stisnjene medicinske pline in podtlak (ISO 9170-1:2008)

General Information

• Status: Withdrawn
• Publication Date: 30-Jun-2008
• Withdrawal Date: 16-Jun-2020
• ICS: 11.040.10 - Anaesthetic, respiratory and reanimation equipment
• Technical Committee: CEN/TC 215 - Respiratory and anaesthetic equipment
• Drafting Committee: CEN/TC 215/WG 3 - Medical gas supply systems
• Current Stage: 9960 - Withdrawal effective - Withdrawal
• Completion Date: 17-Jun-2020
• 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 9170-1:2008 - Terminal units for medical gas pipeline systems - Part 1: Terminal units for use with compressed medical gases and vacuum (ISO 9170-1:2008)

Relations

• Replaces: EN 737-1:1998 - Medical gas pipeline systems - Part 1: Terminal units for compressed medical gases and vacuum
• Effective Date: 22-Dec-2008
• Replaced By: EN ISO 9170-1:2020 - Terminal units for medical gas pipeline systems - Part 1: Terminal units for use with compressed medical gases and vacuum (ISO 9170-1:2017)
• Effective Date: 17-Sep-2014

Standards Content (Sample)

SLOVENSKI STANDARD
01-september-2008
1DGRPHãþD
SIST EN 737-1:2000
.RQþQLGHOLQDSHOMDY]DPHGLFLQVNHSOLQHGHO.RQþQLGHOL]DVWLVQMHQH
PHGLFLQVNHSOLQHLQSRGWODN,62
Terminal units for medical gas pipeline systems - Part 1: Terminal units for use with
compressed medical gases and vacuum (ISO 9170-1:2008)
Entnahmestellen für Rohrleitungssysteme für medizinische Gase - Teil 1:
Entnahmestellen für medizinische Druckgase und Vakuum (ISO 9170-1:2008)
Prises murales pour systèmes de distribution de gaz médicaux - Partie 1: Prises murales
pour les gaz médicaux comprimés et le vide (ISO 9170-1:2008)
Ta slovenski standard je istoveten z: EN ISO 9170-1:2008
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

EUROPEAN STANDARD
EN ISO 9170-1
NORME EUROPÉENNE
EUROPÄISCHE NORM
July 2008
ICS 11.040.10 Supersedes EN 737-1:1998
English Version
Terminal units for medical gas pipeline systems - Part 1:
Terminal units for use with compressed medical gases and
vacuum (ISO 9170-1:2008)
Prises murales pour systèmes de distribution de gaz Entnahmestellen für Rohrleitungssysteme für medizinische
médicaux - Partie 1: Prises murales pour les gaz médicaux Gase - Teil 1: Entnahmestellen für medizinische Druckgase
comprimés et le vide (ISO 9170-1:2008) und Vakuum (ISO 9170-1:2008)
This European Standard was approved by CEN on 21 June 2008.
CEN members are bound to comply with the CEN/CENELEC Internal Regulations which stipulate the conditions for giving this European
Standard the status of a national standard without any alteration. Up-to-date lists and bibliographical references concerning such national
standards may be obtained on application to the CEN Management Centre or to any CEN member.
This European Standard 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 Management Centre has the same status as the
official versions.
CEN members are the national standards bodies of Austria, Belgium, Bulgaria, 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: rue de Stassart, 36  B-1050 Brussels
© 2008 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 9170-1:2008: E
worldwide for CEN national Members.

Contents Page
Foreword.3
Annex ZA (informative) Correspondence between this International Standard and Directive
93/42/EEC.4

Foreword
This document (EN ISO 9170-1:2008) 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 January 2009, and conflicting national standards shall be withdrawn at
the latest by July 2010.
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 supersedes EN 737-1:1998.
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 EC Directive.
For relationship with EC Directives, 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, 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 9170-1:2008 has been approved by CEN as a EN ISO 9170-1:2008 without any modification.
Annex ZA
(informative)
Correspondence between this International Standard and
Directive 93/42/EEC
This International Standard has been prepared under a mandate given to CEN by the European Commission
and the European Free Trade Association to provide one means of conforming to Essential Requirements of
the New Approach Directive 93/42/EEC Medical devices.

Once this standard is cited in the Official Journal of the European Communities under that Directive and has
been implemented as a national standard in at least one Member State, compliance with the normative
clauses of this standard given in Table ZA.1 confers, within the limits of the scope of this standard, a
presumption of conformity with the corresponding Essential Requirements of that Directive and associated
EFTA regulations.
Table ZA.1 — Correspondence between this International Standard and Directive 93/42/EEC
Clause(s)/Sub-clause(s) of Corresponding essential requirements Qualifying remarks/Notes
this International Standard of EU Directive 93/42/EEC
4 1
4.1 2, 6
4.2 2
4.3 2
4.3.1 7.1, 7.3, 9.3
4.3.2 4, 7.1, 9.2
4.3.3 3, 5
4.3.4 7.1, 7.2
4.3.5 7.3, 9.3
4.4 2, 3, 4
4.4.1 9.1, 9.2
4.4.1.2 12.7.1
4.4.1.5 12.7.1
4.4.1.8 12.7.1
4.4.2 9.1, 12.7.4
4.4.3 12.7.4
4.4.4 9.1, 12.7.4
4.4.5 12.8.2
4.4.6 12.8.2
4.4.7 9.1, 12.7.4
4.4.8 12.7.4
4.4.10 12.7.4
Table ZA.1 (continued)
Clause(s)/Sub-clause(s) of Corresponding essential requirements Qualifying remarks/Notes
this International Standard of EU Directive 93/42/EEC
4.4.11 9.1
4.4.12 9.2, 12.7.4
4.4.13 9.2, 12.7.4
4.4.14 9.2, 12.7.1, 12.7.4
4.4.15 7.5
4.4.16 9.1, 12.7.4
4.4.17 9.1, 12.7.4
4.4.18 12.6
4.5.1 7.2, 9.3
4.5.2 7.3, 9.3
5.2 12.7.4
5.3 9.1
5.4 9.2, 12.7.4
5.5 9.2, 12.7.4
5.6 9.2, 12.7.1, 12.7.4
5.7 7.5
5.8 9.1, 12.7.4
5.9 9.1, 12.7.4
5.10 13.2
6.1 13.2
6.1.3 13.1, 13.3 a), 13.3 d), 13.5
6.2 13.2
6.3 3, 5
6.3.1 5, 7.2, 7.6
6.3.2 13.1, 13.3 b)
7.1 13.1, 13.3 a), 13.4, 13.6 a)
7.2 7.6, 9.1, 12.7.4, 13.6 c), 13.6 d)
7.3 2, 13.1
7.4 1st dash 9.3
7.4 2nd dash 9.2
7.4 3rd dash 9.1, 12.7.4, 13.6 c)
WARNING: Other requirements and other EU Directives may be applicable to the products falling within the
scope of this standard.
INTERNATIONAL ISO
STANDARD 9170-1
Second edition
2008-07-01
Terminal units for medical gas pipeline
systems —
Part 1:
Terminal units for use with compressed
medical gases and vacuum
Prises murales pour systèmes de distribution de gaz médicaux —
Partie 1: Prises murales pour les gaz médicaux comprimés et le vide

Reference number
ISO 9170-1:2008(E)
©
ISO 2008
ISO 9170-1:2008(E)
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ISO 9170-1:2008(E)
Contents Page
Foreword .iv
Introduction.v
1 Scope.1
2 * Normative references .2
3 Terms and definitions .2
4 General requirements .6
4.1 Safety.6
4.2 * Alternative construction.6
4.3 Materials .6
4.4 Design requirements.7
4.5 Constructional requirements .10
5 Test methods .11
5.1 General .11
5.2 Test for endurance .11
5.3 Test for pressure drop .12
5.4 Test for connection force and torque.13
5.5 Test for disconnection force and torque .14
5.6 Test for mechanical strength .14
5.7 Test for leakage .14
5.8 Test for gas specificity.15
5.9 Test for effective connection of probes.15
5.10 Test for durability of markings and colour coding .15
6 Marking, colour coding and packaging.15
6.1 Marking.15
6.2 Colour coding .16
6.3 Packaging.16
7 Information to be supplied by the manufacturer .16
Annex A (informative) Rationale.17
Annex B (informative) Environmental aspects .18
Annex C (informative) Special national and regional conditions for electrical installations.19
Bibliography.20

ISO 9170-1:2008(E)
Foreword
ISO (the Interna
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