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EN ISO 3630-4:2009

Withdrawn

Withdrawn

A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.

Dentistry - Root canal instruments - Part 4: Auxiliary instruments (ISO 3630-4:2009)

Withdrawn date

31-01-2010

Published date

01-07-2009

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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

ISO 3630-4:2009 specifies 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.ISO 3630-4:2009 specifies requirements for size, product designation, safety considerations, instructions and labelling.

Committee
CEN/TC 55
DocumentType
Standard
PublisherName
Comite Europeen de Normalisation
Status
Withdrawn

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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