Terminal units for medical gas pipeline systems - Part 2: Terminal units for anaesthetic gas scavenging systems (ISO 9170-2:2008)

ISO 9170-2:2008 specifies the requirements and dimensions for terminal units intended for use in anaesthetic gas scavenging disposal systems in accordance with ISO 7396-2.
ISO 9170-2:2008 specifies two types of terminal unit according to whether the power device is upstream or downstream of the terminal unit.
ISO 9170-2:2008 also specifies requirements and dimensions for the mating counterpart (probe) of the type-specific connection point which is part of the terminal unit.

Entnahmestellen für Rohrleitungssysteme für medizinische Gase - Teil 2: Entnahmestellen für Anästhesiegas-Fortleitungssysteme (ISO 9170-2:2008)

1.1 Dieser Teil von ISO 9170 legt die Anforderungen und Maße für Entnahmestellen fest, die zur Verwendung in Anästhesiegas-Fortleitungssystemen zur Entsorgung nach ISO 7396-2 vorgesehen sind.
1.2 In diesem Teil von ISO 9170 werden zwei Typen von Entnahmestellen spezifiziert, je nachdem, ob sich die Antriebseinrichtung in Strömungsrichtung vor oder hinter der Entnahmestelle befindet.
1.3 Dieser Teil von ISO 9170 legt auch Anforderungen und Maße für das passende Gegenstück (Stecker) der typspezifischen Verbindungsstelle fest, die Teil einer Entnahmestelle ist.
1.4 Dieser Teil von ISO 9170 legt nicht die Bereiche für Nenn-Betriebsdrücke für Entnahmestellen fest, die in ISO 7396-2 festgelegt sind.
1.5 Dieser Teil der ISO 9170 legt nicht die Anforderungen an Entnahmestellen für medizinische Druckgase und Vakuum fest, die in ISO 9170-1 behandelt werden.

Prises murales pour systèmes de distribution de gaz médicaux - Partie 2: Prises murales pour systèmes d'évacuation des gaz d'anesthésie (ISO 9170-2:2008)

L'ISO 9170-2:2008 spécifie les exigences et les dimensions des prises murales destinées à être utilisées dans les systèmes d'évacuation des gaz d'anesthésie conformément à l'ISO 7396-2.
L'ISO 9170-2:2008 spécifie deux types de prises murales pour une utilisation où le dispositif moteur se trouve soit en amont soit en aval de la prise murale.
L'ISO 9170-2:2008 spécifie également les exigences et les dimensions des contreparties s'y emboîtant (embout) du raccord de type spécifique qui fait partie de la prise murale.

Končni deli napeljav za medicinske pline - 2. del: Končni deli sistemov za odstranjevanje anestezijskih plinov in hlapov (ISO 9170-2:2008)

General Information

Status
Published
Publication Date
30-Jun-2008
Withdrawal Date
30-Jul-2010
Current Stage
6060 - Definitive text made available (DAV) - Publishing
Start Date
01-Jul-2008
Due Date
06-Jan-2008
Completion Date
01-Jul-2008

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Standards Content (Sample)


SLOVENSKI STANDARD
01-september-2008
1DGRPHãþD
SIST EN 737-4:2000
.RQþQLGHOLQDSHOMDY]DPHGLFLQVNHSOLQHGHO.RQþQLGHOLVLVWHPRY]D
RGVWUDQMHYDQMHDQHVWH]LMVNLKSOLQRYLQKODSRY ,62
Terminal units for medical gas pipeline systems - Part 2: Terminal units for anaesthetic
gas scavenging systems (ISO 9170-2:2008)
Entnahmestellen für Rohrleitungssysteme für medizinische Gase - Teil 2:
Entnahmestellen für Anästhesiegas-Fortleitungssysteme (ISO 9170-2:2008)
Prises murales pour réseaux de distribution de gaz médicaux - Partie 2: Prises murales
pour systemes d'évacuation des gaz d'anesthésie (ISO 9170-2:2008)
Ta slovenski standard je istoveten z: EN ISO 9170-2:2008
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 9170-2
NORME EUROPÉENNE
EUROPÄISCHE NORM
July 2008
ICS 11.040.10 Supersedes EN 737-4:1998
English Version
Terminal units for medical gas pipeline systems - Part 2:
Terminal units for anaesthetic gas scavenging systems (ISO
9170-2:2008)
Prises murales pour systèmes de distribution de gaz Entnahmestellen für Rohrleitungssysteme für medizinische
médicaux - Partie 2: Prises murales pour systèmes Gase - Teil 2: Entnahmestellen für Anästhesiegas-
d'évacuation des gaz d'anesthésie (ISO 9170-2:2008) Fortleitungssysteme (ISO 9170-2:2008)
This European Standard was approved by CEN on 15 May 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 9170-2:2008: 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 9170-2:2008) 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 737-4:1998.
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 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, 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 9170-2:2008 has been approved by CEN as a EN ISO 9170-2:2008 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, 9.2
4.3.3 3, 5
4.4 2, 3, 4
4.4.1 12.7.4
4.4.2 9.1, 12.7.4
4.4.3 12.8.2
4.4.4 9.1, 12.7.4
4.4.5 9.1, 12.7.4
4.4.6 12.7.4
4.4.8 9.1
4.4.9 9.2, 12.7.4
4.4.10 9.2, 12.7.4
4.4.11 9.2, 12.7.1, 12.7.4
4.4.12 7.5
4.4.13 9.1, 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
4.4.14 9.1, 12.7.4
4.4.15 12.7.4
4.4.16 9.1, 12.7.4
4.4.17 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 9.2, 12.7.1, 12.7.4
5.11 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, 13.6 d), 13.6 h)
7.4 1st dash 9.3
7.4 2nd dash 9.2, 13.6 I)
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 9170-2
Second edition
2008-07-01
Terminal units for medical gas pipeline
systems —
Part 2:
Terminal units for anaesthetic gas
scavenging systems
Prises murales pour systèmes de distribution de gaz médicaux —
Partie 2: Prises murales pour systèmes d'évacuation des gaz
d'anesthésie
Reference number
ISO 9170-2:2008(E)
©
ISO 2008
ISO 9170-2:2008(E)
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ISO 9170-2:2008(E)
Contents Page
Foreword .iv
Introduction.v
1 Scope.1
2 * Normative references .1
3 Terms and definitions .3
4 General requirements .7
4.1 Safety.7
4.2 * Alternative construction.7
4.3 Materials .7
4.4 Design requirements.7
4.5 Construction requirements .14
5 Test methods .14
5.1 General .14
5.2 Endurance test.14
5.3 Test method for pressure drop .15
5.4 Test method for connection force .15
5.5 Test method for disconnection force .15
5.6 Tests for mechanical strength .16
5.7 Tests for leakage .16
5.8 Test for type specificity .16
5.9 Test for effective connection of probes to sockets .16
5.10 Test for connection of receiving or disposal hoses to hose inserts .16
5.11 Test for durability of markings and colour coding .16
6 Marking, colour coding and packaging.16
6.1 Marking.16
6.2 Colour coding .17
6.3 Packaging.17
7 Information to be supplied by the manufacturer .17
Annex A (informative) Rationale.18
Annex B (informative) Environmental aspects .19
Annex C (informative) Special national and regional conditions for electrical installations.21
Bibliography.22
...

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