I.S. EN 12470-2:2000
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
CLINICAL THERMOMETERS - PART 2: PHASE CHANGE TYPE (DOT MATRIX) THERMOMETERS
Hardcopy , PDF
19-08-2009
English
02-02-2001
For Harmonized Standards, check the EU site to confirm that the Standard is cited in the Official Journal.
Only cited Standards give presumption of conformance to New Approach Directives/Regulations.
Dates of withdrawal of national standards are available from NSAI.
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Foreword
1 Scope
2 Normative references
3 Terms and definitions
4 Unit
5 Type of thermometers
6 Requirements
7 Test methods
8 Information supplied by the manufacturer
Annex A (informative) - Suggested types of testing for the
requirements of this standard
Annex ZA (informative) - Relationship between this European
Standard and the Essential
Requirements of EU Directive
93/42/EEC
Bibliography
Describes performance requirements and test methods for phase change-type (dot matrix) thermometers for measuring temperature in body cavities.
| DevelopmentNote |
2001 Edition Re-Issued in August 2009 & incorporates AMD 1 2009. (08/2009)
|
| DocumentType |
Standard
|
| Pages |
19
|
| PublisherName |
National Standards Authority of Ireland
|
| Status |
Withdrawn
|
| Standards | Relationship |
| NF EN 12470-2 : 2000 + A1 2009 | Identical |
| DIN EN 12470-2:2009-11 | Identical |
| NBN EN 12470-2 : 2001 + A1 2009 | Identical |
| EN 12470-2:2000+A1:2009 | Identical |
| NS EN 12470-2 : 2000 + A1 2009 | Identical |
| UNI EN 12470-2 : 2009 | Identical |
| BS EN 12470-2 : 2001 | Identical |
| UNE-EN 12470-2:2001 | Identical |
| NEN EN 12470-2 : 2000 + A1 2009 | Identical |
| SN EN 12470-2 : 2001 + A1 2009 | Identical |
| EN 556:1994 + A1:1998 | STERILIZATION OF MEDICAL DEVICES - REQUIREMENTS FOR TERMINALLY-STERILIZED MEDICAL DEVICES TO BE LABELLED "STERILE" |
| ISO/IEC Guide 98:1993 | Guide to the expression of uncertainty in measurement (GUM) |
| ISO 2859-2:1985 | Sampling procedures for inspection by attributes — Part 2: Sampling plans indexed by limiting quality (LQ) for isolated lot inspection |
| 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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