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BS 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Superseded

Superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.

View Superseded by
superseded

A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.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

Available format(s)

Hardcopy , PDF

Superseded date

23-08-2023

Language(s)

English

Published date

31-07-2009

This part of ISO3630 specifies requirements and test methods for hand-held or mechanically operated instruments for performing root canal procedures not cited in ISO3630-1, 3630-2, 3630-3 or 3630-5.

This part of ISO3630 specifies requirements for size, product designation, safety considerations, instructions and labelling.

Committee
CH/106/4
DevelopmentNote
Supersedes 08/30168812 DC. (07/2009) Reviewed and confirmed by BSI, February 2015. (01/2015)
DocumentType
Standard
Pages
18
PublisherName
British Standards Institution
Status
Superseded
SupersededBy
Supersedes

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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