SIST EN 12470-3:2000/kprA1:2009

Clinical thermometers - Part 3: Performance of compact electrical thermometers (non-predictive and predictive) with maximum device

Medizinische Thermometer - Teil 3: Elektrische (extrapolierende und nicht extrapolierende) Kompaktthermometer mit Maximumvorrichtung

Thermomètres médicaux - Partie 3: Performances des thermomètres électriques compacts (à comparaison et à extrapolation) avec dispositif à maximum

Klinični termometri - 3. del: Delovanje zaprtih trdnih električnih termometrov (brez umerjanja ali z njim)

General Information

• Status: Not Published
• Public Enquiry End Date: 09-Apr-2009
• ICS: 11.040.55 - Diagnostic equipment
• Technical Committee: VAZ - Healthcare
• Current Stage: 98 - Abandoned project (Adopted Project)
• Start Date: 11-May-2012
• Due Date: 16-May-2012
• Completion Date: 11-May-2012
• Directive: 2007/47/EC - Directive 2007/47/EC of the European Parliament and of the council of 5 September 2007 amending Council Directive 90/385/EEC on the approximation of the laws of the Member States relating to active implantable medical devices, Council Directive 93/42/EEC concerning medical devices and Directive 98/8/EC concerning the placing of biocidal products on the market
• 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: EN 12470-3:2000/prA1 - Clinical thermometers - Part 3: Performance of compact electrical thermometers (non-predictive and predictive) with maximum device

Relations

• Consolidated By: SIST EN 12470-3:2000+A1:2009 - Clinical thermometers - Part 3: Performance of compact electrical thermometers (non-predictive and predictive) with maximum device
• Effective Date: 18-Jan-2023
• Consolidated By: SIST EN 12470-3:2000+A1:2009 - Clinical thermometers - Part 3: Performance of compact electrical thermometers (non-predictive and predictive) with maximum device
• Effective Date: 19-Jan-2023
• Amends: SIST EN 12470-3:2000 - Clinical thermometers - Part 3: Performance of compact electrical thermometers (non-predictive and predictive) with maximum device
• Effective Date: 01-Apr-2009
• Consolidated By: SIST EN 12470-3:2000+A1:2009 - Clinical thermometers - Part 3: Performance of compact electrical thermometers (non-predictive and predictive) with maximum device
• Effective Date: 01-Oct-2009

Standards Content (Sample)

SLOVENSKI STANDARD
SIST EN 12470-3:2000/kprA1:2009
01-april-2009
.OLQLþQLWHUPRPHWULGHO'HORYDQMH]DSUWLKWUGQLKHOHNWULþQLKWHUPRPHWURYEUH]
XPHUMDQMDDOL]QMLP
Clinical thermometers - Part 3: Performance of compact electrical thermometers (non-
predictive and predictive) with maximum device
Medizinische Thermometer - Teil 3: Elektrische (extrapolierende und nicht
extrapolierende) Kompaktthermometer mit Maximumvorrichtung
Thermomètres médicaux - Partie 3: Performances des thermomètres électriques
compacts (à comparaison et à extrapolation) avec dispositif à maximum
Ta slovenski standard je istoveten z: EN 12470-3:2000/prA1
ICS:
11.040.55 'LDJQRVWLþQDRSUHPD Diagnostic equipment
SIST EN 12470-3:2000/kprA1:2009 en,fr
2003-01.Slovenski inštitut za standardizacijo. Razmnoževanje celote ali delov tega standarda ni dovoljeno.

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SIST EN 12470-3:2000/kprA1:2009

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SIST EN 12470-3:2000/kprA1:2009
EUROPEAN STANDARD
FINAL DRAFT
EN 12470-3:2000
NORME EUROPÉENNE
EUROPÄISCHE NORM
prA1
January 2009
ICS 17.200.20

English Version
Clinical thermometers - Part 3: Performance of compact
electrical thermometers (non-predictive and predictive) with
maximum device
Thermomètres médicaux - Partie 3: Performances des Medizinische Thermometer - Teil 3: Elektrische
thermomètres électriques compacts (à comparaison et à (extrapolierende und nicht extrapolierende)
extrapolation) avec dispositif à maximum Kompaktthermometer mit Maximumvorrichtung
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 12470-3:2000. 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 12470-3:2000/prA1:2009: E
worldwide for CEN national Members.

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SIST EN 12470-3:2000/kprA1:2009
EN 12470-3:2000/prA1:2009 (E)
Contents Page
Foreword .3
1 Modification to Clause 2, Normative references .4
2 Modification to 6.1, Probe cover .4
3 Modification to 8.1, General .4
4 Modification to 8.2, Marking .4
5 Modification to 8.3, Instructions for use.4
6 Modification to Annex ZA .5

2

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SIST EN 12470-3:2000/kprA1:2009
EN 12470-3:2000/prA1:2009 (E)
Foreword
This document (EN 12470-3:2000/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
Europe
...