Rail systems for supporting medical equipment (ISO 19054:2005/Amd 1:2016)

DOW = DAV + 36 months

Schienensysteme zum Halten medizinischer Geräte (ISO 19054:2005/Amd 1:2016)

Systèmes de rails de support pour appareils médicaux (ISO 19054:2005/Amd 1:2016)

Tračni nosilci za pritrditev medicinske opreme (ISO 19054:2005/Amd 1:2016)

General Information

Status
Published
Public Enquiry End Date
09-May-2016
Publication Date
10-Jan-2017
Technical Committee
Current Stage
6060 - National Implementation/Publication (Adopted Project)
Start Date
16-Dec-2016
Due Date
20-Feb-2017
Completion Date
11-Jan-2017

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EN ISO 19054:2006/A1:2017
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Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN ISO 19054:2006/A1:2017
01-februar-2017
7UDþQLQRVLOFL]DSULWUGLWHYPHGLFLQVNHRSUHPH ,62$PG
Rail systems for supporting medical equipment (ISO 19054:2005/Amd 1:2016)
Schienensysteme zum Halten medizinischer Geräte (ISO 19054:2005/Amd 1:2016)
Systèmes de rails de support pour appareils médicaux (ISO 19054:2005/Amd 1:2016)
Ta slovenski standard je istoveten z: EN ISO 19054:2006/A1:2016
ICS:
11.040.99 Druga medicinska oprema Other medical equipment
SIST EN ISO 19054:2006/A1:2017 en
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN ISO 19054:2006/A1:2017

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SIST EN ISO 19054:2006/A1:2017


EN ISO 19054:2006/A1
EUROPEAN STANDARD

NORME EUROPÉENNE

December 2016
EUROPÄISCHE NORM
ICS 11.040.99
English Version

Rail systems for supporting medical equipment (ISO
19054:2005/Amd 1:2016)
Systèmes de rails de support pour appareils médicaux Schienensysteme zum Halten medizinischer Geräte
(ISO 19054:2005/Amd 1:2016) (ISO 19054:2005/Amd 1:2016)
This amendment A1 modifies the European Standard EN ISO 19054:2006; it was approved by CEN on 30 November 2016.

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, 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
© 2016 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN ISO 19054:2006/A1:2016 E
worldwide for CEN national Members.

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SIST EN ISO 19054:2006/A1:2017
EN ISO 19054:2006/A1:2016 (E)
Contents Page
Eurpopean foreword . 3
Annex ZA (informative) Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC [OJ L 169] aimed to be covered . 4

2

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SIST EN ISO 19054:2006/A1:2017
EN ISO 19054:2006/A1:2016 (E)
Eurpopean foreword
This document (EN ISO 19054:2006/A1:2016) 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 Amendment to the European Standard EN ISO 19054:2006 shall be given the status of a national
standard, either by publication of an identical text or by endorsement, at the latest by June 2017, and
conflicting national standards shall be withdrawn at the latest by June 2017.
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(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, 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, Slovakia, Slovenia, Spain, Sweden, Switzerland, Turkey and the
United Kingdom.
Endorsement notice
The text of ISO 19054:2005/Amd1:2016 has been approved by CEN as EN ISO 19054:2006/A1:2016
without any modification.
3

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SIST EN ISO 19054:2006/A1:2017
EN ISO 19054:2006/A1:2016 (E)
Annex ZA
(informative)

Relationship between this European Standard and the Essential
Requirements of EU Directive 93/42/EEC [OJ L 169] aimed to be covered
This European Standard has been prepared under a Commission’s standardization request [M/023
concerning the development of European Standards related to medical devices] / [M/295 concerning
the development of European Standards related to medical devices] / [reference number and title of
any other standardization request as relevant] to provide one voluntary means of conforming to
essential requirements of Council Directive 93/42/EEC of 14 June 1993 concerning medical devices [OJ
L 160].
Once this standard is cited in the Official Journal of the European Union under that Directive,
...

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