SN EN 1639:2010
Current
The latest, up-to-date edition.
DENTISTRY - MEDICAL DEVICES FOR DENTISTRY - INSTRUMENTS
Hardcopy
01-03-2010
Foreword
1 Scope
2 Normative references
3 Terms and definitions
4 Requirements
4.1 General
4.2 Chemical and physical properties
4.2.1 General
4.2.2 Contaminants and residues
4.2.3 Contact with substances
4.3 Control of contamination
4.3.1 General
4.3.2 Instruments supplied sterile
4.3.3 Instruments supplied non-sterile
4.4 Construction and environmental properties
4.5 Instruments connected to or equipped with an energy source
4.6 Protection against electrical risks
4.7 Protection against mechanical and thermal risks
4.7.1 Vibration
4.7.2 Noise
4.7.3 Electricity, gas or hydraulic and pneumatic energy
4.7.4 Surface temperature
4.8 Controls and indicators
4.9 Marking, labelling and information supplied by the manufacturer
4.9.1 General
4.9.2 Symbols
4.9.3 Marking
4.9.4 Labelling
4.9.5 Detachable components
4.9.6 Instructions for use
Annex ZA (informative) Relationship between this European Standard
and the Essential Requirements of EU Directive 93/42/EEC
Bibliography
This European Standard specifies general requirements for instruments used in the practice of dentistry and which are medical devices.
Committee |
INB/NK 155
|
DocumentType |
Standard
|
Pages |
0
|
PublisherName |
Swiss Standards
|
Status |
Current
|
Standards | Relationship |
UNE-EN 1639:2010 | Identical |
EN 1639:2009 | Identical |
NEN EN 1639 : 2009 | Identical |
NS EN 1639 : 2009 | Identical |
I.S. EN 1639:2009 | Identical |
NF EN 1639 : 2009 | Identical |
DIN EN 1639:2010-02 | Identical |
NBN EN 1639 : 2009 | Identical |
UNI EN 1639 : 2010 | Identical |
BS EN 1639:2009 | Identical |
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