BS 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Superseded
A superseded Standard is one, which is fully replaced by another Standard, which is a new edition of the same Standard.
View Superseded by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 Auxiliary instruments
Hardcopy , PDF
English
31-07-2009
23-08-2023
| Committee |
CH/106
|
| 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Superseded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 |
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.
| Standards | Relationship |
| EN ISO 3630-4:2009 | Identical |
| ISO 3630-4:2009 | Identical |
| I.S. EN ISO 3630-4:2009 | Equivalent |
| DIN EN ISO 3630-4:2009-10 | Equivalent |
| 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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