UNI EN ISO 3630-4 : 2009
Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by
DENTISTRY - ROOT CANAL INSTRUMENTS - PART 4: AUXILIARY INSTRUMENTS
25-10-2023
08-10-2009
Foreword
1 Scope
2 Normative references
3 Terms, definitions and symbols
3.1 Terms and definitions
3.2 Symbols
4 Classification
5 Requirements
5.1 Material
5.2 Dimensions
5.3 Colour designation and size marking with rings
5.4 Mechanical requirements
5.5 Resistance to corrosion
5.6 Heat effects of sterilization
6 Sampling
7 Testing
7.1 General
7.2 Dimensions
8 Designation, marking and identification
9 Packaging
10 Labelling
Bibliography
Describes requirements and test methods for hand-held or mechanically operated instruments for performing root canal procedures not cited in ISO 3630-1, 3630-2, 3630-3 or 3630-5.
| Committee |
CT 44
|
| DocumentType |
Standard
|
| PublisherName |
Ente Nazionale Italiano di Unificazione (UNI)
|
| Status |
Superseded
|
| SupersededBy |
| Standards | Relationship |
| EN ISO 3630-4:2009 | Identical |
| ISO 3630-4:2009 | Identical |
| ISO 1797-2:1992 | Dental rotary instruments Shanks Part 2: Shanks made of plastics |
| ISO 6360-2:2004 | Dentistry — Number coding system for rotary instruments — Part 2: Shapes |
| ISO 6360-5:2007 | Dentistry — Number coding system for rotary instruments — Part 5: Specific characteristics of root-canal instruments |
| ISO 6360-1:2004 | Dentistry — Number coding system for rotary instruments — Part 1: General characteristics |
| ISO 1797-1:2011 | Dentistry Shanks for rotary instruments Part 1: Shanks made of metals |
| ISO 1942:2009 | Dentistry Vocabulary |
| ISO 3630-2:2013 | Dentistry — Endodontic instruments — Part 2: Enlargers |
| ISO 3630-1:2008 | Dentistry Root-canal instruments Part 1: General requirements and test methods |
| ISO 15223-1:2016 | Medical devices Symbols to be used with medical device labels, labelling and information to be supplied Part 1: General requirements |
| ISO 17664:2017 | Processing of health care products Information to be provided by the medical device manufacturer for the processing of medical devices |
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