SIST EN 12470-4:2001/kprA1:2009
(Amendment)Clinical thermometers - Part 4: Performance of electrical thermometers for continuous measurement
Clinical thermometers - Part 4: Performance of electrical thermometers for continuous measurement
Medizinische Thermometer - Teil 4: Anforderungen an elektrische Thermometer zur kontinuierlichen Messung
Thermomètres médicaux - Partie 4: Performances des thermomètres électriques de mesurage continu
Klinični termometri - 4. del: Delovanje električnih termometrov za nepretrgano merjenje
General Information
Relations
Standards Content (Sample)
SLOVENSKI STANDARD
SIST EN 12470-4:2001/kprA1:2009
01-april-2009
.OLQLþQLWHUPRPHWULGHO'HORYDQMHHOHNWULþQLKWHUPRPHWURY]DQHSUHWUJDQR
PHUMHQMH
Clinical thermometers - Part 4: Performance of electrical thermometers for continuous
measurement
Medizinische Thermometer - Teil 4: Anforderungen an elektrische Thermometer zur
kontinuierlichen Messung
Thermomètres médicaux - Partie 4: Performances des thermomètres électriques de
mesurage continu
Ta slovenski standard je istoveten z: EN 12470-4:2000/prA1
ICS:
11.040.55 'LDJQRVWLþQDRSUHPD Diagnostic equipment
SIST EN 12470-4:2001/kprA1:2009 en,fr
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.
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SIST EN 12470-4:2001/kprA1:2009
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SIST EN 12470-4:2001/kprA1:2009
EUROPEAN STANDARD
FINAL DRAFT
EN 12470-4:2000
NORME EUROPÉENNE
EUROPÄISCHE NORM
prA1
January 2009
ICS 17.200.20
English Version
Clinical thermometers - Part 4: Performance of electrical
thermometers for continuous measurement
Thermomètres médicaux - Partie 4: Fonctionnement des Medizinische Thermometer - Teil 4: Anforderungen an
thermomètres électriques de mesurage continu elektrische Thermometer zur kontinuierlichen Messung
This draft amendment is submitted to CEN members for unique acceptance procedure. It has been drawn up by the Technical Committee
CEN/TC 205.
This draft amendment A1, if approved, will modify the European Standard EN 12470-4:2000. If this draft becomes an amendment, 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.
This draft amendment was established by CEN 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.
Warning : This document is not a European Standard. It is distributed for review and comments. It is subject to change without notice and
shall not be referred to as a European Standard.
EUROPEAN COMMITTEE FOR STANDARDIZATION
COMITÉ EUROPÉEN DE NORMALISATION
EUROPÄISCHES KOMITEE FÜR NORMUNG
Management Centre: Avenue Marnix 17, B-1000 Brussels
© 2009 CEN All rights of exploitation in any form and by any means reserved Ref. No. EN 12470-4:2000/prA1:2009: E
worldwide for CEN national Members.
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SIST EN 12470-4:2001/kprA1:2009
EN 12470-4:2000/prA1:2009 (E)
Contents Page
Foreword .3
1 Modification to Clause 2, Normative references .4
2 Modification to 8.1, General .4
3 Modification to 8.2.1, Complete thermometer .4
4 Modification to 8.2.2, Temperature probe .4
5 Modification to 8.2.3, Indicating unit.4
6 Modification to 8.3, Instructions for use.5
7 Modification to Annex ZA .5
2
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SIST EN 12470-4:2001/kprA1:2009
EN 12470-4:2000/prA1:2009 (E)
Foreword
This document (EN 12470-4:2000/prA1:2009) has been prepared by Technical Committee CEN/TC 205 “Non-
active medical devices”, the secretariat of which is held by DIN.
This document is currently submitted to the Unique Acceptance Procedure.
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, see informative Annex ZA, which is an integral part of this document.
This European Standard applies to clinical thermometers which are used for meas
...
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