DIN EN 12470-3:2000-04
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
CLINICAL THERMOMETERS - PART 3: PERFORMANCE OF COMPACT ELECTRICAL THERMOMETERS (NON-PREDICTIVE AND PREDICTIVE) WITH MAXIMUM DEVICE
Hardcopy , PDF
English
01-01-2000
01-02-2013
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
National Annex NA (informative) Bibliography
Describes the performance requirements for compact clinical electrical thermometers with maximum device (non-predictive and predictive).
| DocumentType |
Standard
|
| Pages |
22
|
| PublisherName |
German Institute for Standardisation (Deutsches Institut für Normung)
|
| Status |
Superseded
|
| Standards | Relationship |
| NS EN 12470-3 : 2000 + A1 2009 | Identical |
| NF EN 12470-3 : 2000 + A1 2009 | Identical |
| 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 |
| I.S. EN 12470-3:2000 | Identical |
| 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 |
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