I.S. EN 12470-2:2000
Withdrawn
CLINICAL THERMOMETERS - PART 2: PHASE CHANGE TYPE (DOT MATRIX) THERMOMETERS
Hardcopy , PDF
English
02-02-2001
08-19-2009
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.
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Withdrawn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 |
| BS EN 12470-2 : 2001 | Identical |
| NEN EN 12470-2 : 2000 + A1 2009 | Identical |
| UNE-EN 12470-2:2001 | 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 |
Please Login or Create an Account so you can add users to your Multi user PDF Later.
Important note : All end users must be registered with an Account prior to user licenses being assigned.
Users cannot be edited or removed once added to your Multi user PDF.