UNI EN 12470-3 : 2009

Name: UNI EN 12470-3 : 2009
Brand: UNI

Superseded

View Superseded by

CLINICAL THERMOMETERS - PART 3: PERFORMANCE OF COMPACT ELECTRICAL THERMOMETERS (NON-PREDICTIVE AND PREDICTIVE) WITH MAXIMUM DEVICE

Superseded date

02-21-2013

Published date

01-01-2009

Publisher

Ente Nazionale Italiano di Unificazione (UNI)

Foreword
1 Scope
2 Normative references
3 Definitions
4 Unit
5 Types of thermometers
6 Performance requirements
7 Test methods
8 Information supplied by the manufacturer
Annex A (informative) - Suggested types of testing for the
        requirements of this standard
Annex B (informative) - Bibliography
Annex ZA (informative) - Relationship between this European
         Standard and the Essential Requirements of EU
         Directive 93/42/EEC

Describes the performance requirements for compact clinical electrical thermometers with maximum device (non-predictive and predictive).

DocumentType	Standard
PublisherName	Ente Nazionale Italiano di Unificazione (UNI)
Status	Superseded
SupersededBy	UNI EN ISO 80601-2-56 : 2013
Supersedes	UNI EN 12470-3 : 2001

Standards	Relationship
I.S. EN 12470-3:2000	Identical
EN 12470-3:2000+A1:2009	Identical
SN EN 12470-3 : 2000 + A1 2009	Identical
DIN EN 12470-3:2009-11	Identical
UNE-EN 12470-3:2000	Identical
NS EN 12470-3 : 2000 + A1 2009	Identical
NF EN 12470-3 : 2000 + A1 2009	Identical
BS EN 12470-3 : 2000	Identical
NEN EN 12470-3 : 2000 + A1 2009	Identical
NBN EN 12470-3 : 2000 + A1 2009	Identical
DIN EN 12470-3:2000-04	Identical

ISO/IEC Guide 98:1993	Guide to the expression of uncertainty in measurement (GUM)
IEC 60601-1:2005+AMD1:2012 CSV	Medical electrical equipment - Part 1: General requirements for basic safety and essential performance
ISO 2859-2:1985	Sampling procedures for inspection by attributes — Part 2: Sampling plans indexed by limiting quality (LQ) for isolated lot inspection
EN 60601-1-2:2015	Medical electrical equipment - Part 1-2: General requirements for basic safety and essential performance - Collateral Standard: Electromagnetic disturbances - Requirements and tests
EN 1041:2008+A1:2013	Information supplied by the manufacturer of medical devices
ISO 10993-1:2009	Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process
EN 980:2008	Symbols for use in the labelling of medical devices
EN ISO 10993-1:2009/AC:2010	BIOLOGICAL EVALUATION OF MEDICAL DEVICES - PART 1: EVALUATION AND TESTING WITHIN A RISK MANAGEMENT PROCESS (ISO 10993-1:2009/COR 1:2010)