Rescue systems - Transportation of incubators - Part 1: Interface conditions

This standard specifies the requirements for the interface between the vehicle and the incubator and the associated equipment, needed for care and treatment of neonates, used in emergency or planned transport. The standard also specifies that the equipment or systems used do not interfere with the functions of the vehicle or craft providing transportation.

Rettungssysteme - Inkubatortransport - Teil 1: Anforderungen an Schnittstellen

Diese Europäische Norm legt die Anforderungen an die Schnittstellen zwischen dem Fahrzeug und dem Inkubator sowie der dazugehörigen Ausrüstung fest, die bei Notfall- oder geplanten Transporten für die Pflege und Behandlung von Säuglingen erforderlich ist.
Die Norm legt auch Anforderungen an den sicheren Transport unter Anwendung von Ausrüstungen oder Systemen fest, die nicht störend in die Funktionen des Fahrzeugs eingreifen.
In dieser Norm sind keine Anforderungen an die Fahrzeuge, Geräte oder Inkubatoren selbst festgelegt, diese Anforderungen finden sich in anderen Normen. Transportinkubatoren sind jedoch normalerweise mit anderen Geräten verbunden und bilden ein "Inkubatortransportsystem".

Systemes de sauvetage - Transport d'incubateurs - Partie 1: Conditions d'interface

La présente Norme européenne spécifie les exigences relatives a l'interface entre le véhicule ou l'engin a moteur, l'incubateur et les équipements associés, utilisés pour les soins aux nourrissons dans le cadre d'un transport, d'urgence ou non.
La présente Norme européenne spécifie également les exigences relatives a la sécurité du transport au moyen d'équipements ou de systemes qui n'interferent pas avec les fonctions du moyen de transport.
La présente Norme européenne ne prescrit pas d'exigences relatives aux véhicules, dispositifs ou incubateurs en tant que tels ; ces exigences sont formulées dans d'autres normes. Cependant, les incubateurs de transport sont normalement combinés avec d'autres équipements, pour former un «systeme d'incubateur de transport».

Reševalni sistemi – Prevoz inkubatorjev – 1. del: Vmesni pogoji

General Information

Status
Withdrawn
Publication Date
31-Jan-2004
Withdrawal Date
31-May-2011
Technical Committee
Current Stage
9900 - Withdrawal (Adopted Project)
Start Date
01-Jun-2011
Due Date
24-Jun-2011
Completion Date
01-Jun-2011

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SLOVENSKI STANDARD
SIST EN 13976-1:2004
01-februar-2004
Reševalni sistemi – Prevoz inkubatorjev – 1. del: Vmesni pogoji
Rescue systems - Transportation of incubators - Part 1: Interface conditions
Rettungssysteme - Inkubatortransport - Teil 1: Anforderungen an Schnittstellen
Systemes de sauvetage - Transport d'incubateurs - Partie 1: Conditions d'interface
Ta slovenski standard je istoveten z: EN 13976-1:2003
ICS:
11.040.10 Anestezijska, respiratorna in Anaesthetic, respiratory and
reanimacijska oprema reanimation equipment
11.160 3UYDSRPRþ First aid
SIST EN 13976-1:2004 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN 13976-1:2004

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SIST EN 13976-1:2004
EUROPEAN STANDARD
EN 13976-1
NORME EUROPÉENNE
EUROPÄISCHE NORM
December 2003
ICS 11.040.10; 11.160
English version
Rescue systems - Transportation of incubators - Part 1:
Interface conditions
Systèmes de sauvetage - Transport d'incubateurs - Partie Rettungssysteme - Inkubatortransport - Teil 1:
1: Conditions d'interface Anforderungen an Schnittstellen
This European Standard was approved by CEN on 3 November 2003.
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 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 Management Centre has the same status as the official
versions.
CEN members are the national standards bodies of Austria, Belgium, Czech Republic, Denmark, Finland, France, Germany, Greece,
Hungary, Iceland, Ireland, Italy, Luxembourg, Malta, Netherlands, Norway, Portugal, Slovakia, 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
© 2003 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN 13976-1:2003 E
worldwide for CEN national Members.

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SIST EN 13976-1:2004
EN 13976-1:2003 (E)
Contents
page
Foreword.3
Introduction .4
1 Scope .5
2 Normative references .5
3 Terms and definitions.6
4 Requirements .6
4.1 General requirements for transport incubator systems .6
4.1.1 Vehicles.6
4.1.2 Loading .6
4.1.3 Placement .7
4.2 Interface between transport incubator, medical devices and vehicle.7
4.2.1 Fixation .7
4.2.2 Electricity.7
4.2.3 Gas supply.8
4.2.4 General requirements – gases (transportation).9
Annex ZA (informative) Clauses of this European Standard addressing essential requirements or other
provisions of EU Directives. .10
Table ZA.1 – Correspondence between this European Standard and EU Directives.10
Bibliography .11
2

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SIST EN 13976-1:2004
EN 13976-1:2003 (E)
Foreword
This document (EN 13976-1:2003) has been prepared by Technical Committee CEN /TC 239, "Rescue systems",
the secretariat of which is held by DIN.
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 2004, and conflicting national standards shall be withdrawn at the latest by
June 2004.
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(s).
For relationship with EU Directive(s), 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, Czech Republic, Denmark, Finland,
France, Germany, Greece, Hungary, Iceland, Ireland, Italy, Luxembourg, Malta, Netherlands, Norway, Portugal,
Slovakia, Spain, Sweden, Switzerland and the United Kingdom.
3

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SIST EN 13976-1:2004
EN 13976-1:2003 (E)
Introduction
This European Standard gives the requirements for the interfaces required in the transport of an incubator. These
include those between the incubator and the vehicle or craft as well as those between the various items of
equipment used to make up the transport incubator system. They are essential in order to ensure interchangeability
and a safe and effective function in different vehicles, allowing the uninterrupted care of patients. Requirements for
the system are given in part 2 (EN 13976-2).
Fixation, monitoring, supply of gas and electricity shall be maintained through the use of the same standard
interfaces as defined in this document.
4

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SIST EN 13976-1:2004
EN 13976-1:2003 (E)
1 Scope
This European Standard specifies the requirements for the interface between the vehicle or craft and the incubator
and the associated equipment, needed for care and treatment of infants, used in emergency or planned transport.
The standard also specifies requirements for the safe transportation using equipment or systems that do not
interfere with the functions of the vehicle or craft providing transportation.
This standard does not give requirements for the vehicles, crafts, devices or incubators as such, these
requirements are found in other standards. However, transport incubators are normally combined with other
equipment to form a “transport incubator system”.
2 Normative references
This European Standard incorporates by dated or undated reference, provisions from other publications. These
normative references are cited at the appropriate places in the text and the publications are listed hereafter. For
dated references, subsequent amendments to or revisions of any of these publications apply to this European
Standard only when incorporated in it by amendment or revision. For undated references the latest edition of the
publication referred to applies (including amendments).
EN 737-1, Medical gas pipeline systems — Part 1: Terminal units for compressed medical gases and vacuum.
EN 737-2, Medical gas pipeline systems — Part 2: Anaesthetic gas scavenging disposal systems - Basic
requirements.
EN 737-3, Medical gas pipeline systems — Part 3: Pipelines for compressed medical gases and vacuum
EN 737-4, Medical gas pipeline systems — Part 4: Terminal units for anaesthetic gas scavenging systems.
ENV 737-6 Medical gas pipeline systems — Part 6: Dimensions and allocation of probes for terminal units for
compressed medical gases and vacuum.
EN 740 Anaesthetic workstations and their modules — Particular requirements.
EN 850, Transportable gas cylinders — Pin-index, yoke-type valve outlet connections for medical use.
EN 1789:1999, Medical vehicles and their equipment — Road ambulances.
EN 1865, Specifications for stretchers and other patient handling equipment used in road ambulances.
EN 13718-1, Air, water and difficult terrain ambulances — Part 1: Medical device interface requirements for the
continuity of patient care.
EN 13718-2, Air, water and difficult terrain ambulances — Part 2: Operational and technical requirements for the
continuity of patient care.
EN 13976-2, Rescue systems — Transportation of incubators — Part 2: System requirements.
EN 60309-1, Plugs, socket-outlets and couplers for industrial purposes - Part 1: General requirements (IEC 60309-
1:1999).
EN 60309-2, Plugs, socket-outlets and couplers for industrial purposes - Part 2: Dimensional interchangeability
requirements for pin and contact-tube accessories (IEC 60309-2:1999).
EN 60601-1-1, Medical electrical equipment — Part 1-1: General requirements for safety; Collateral standard:
Safety requirements for medical electrical systems (IEC 60601-1-1:2000).
EN 60601-2-20:1996, Medical electrical equipment — Part 2: Particular requir
...

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