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UNI EN ISO 3630-4 : 2009

Superseded
Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

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superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

DENTISTRY - ROOT CANAL INSTRUMENTS - PART 4: AUXILIARY INSTRUMENTS
Superseded date

10-25-2023

Published date

10-08-2009

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Superseded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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