ISO 19490:2017
Withdrawn
Withdrawn
A Withdrawn Standard is one, which is removed from sale, and its unique number can no longer be used. The Standard can be withdrawn and not replaced, or it can be withdrawn and replaced by a Standard with a different number.
View Superseded by
Dentistry — Sinus membrane elevator
Available format(s)
Hardcopy , PDF
Language(s)
English, French
Published date
23-05-2017
Withdrawn date
02-11-2025
Superseded by
€65.00
Excluding VAT
ISO 19490:2017 specifies requirements and their test methods for sinus membrane elevators used during the placement of dental implants for sinus floor lifting. It also specifies the requirements for their marking and labelling.
| Committee |
ISO/TC 106/SC 4
|
| DevelopmentNote |
Supersedes ISO/DIS 19490. (05/2017)
|
| DocumentType |
Standard
|
| Pages |
5
|
| PublisherName |
International Organization for Standardization
|
| Status |
Withdrawn
|
| SupersededBy |
| Standards | Relationship |
| IS/ISO 19490 : 2017 | Identical |
| DIN EN ISO 19490:2017-09 | Identical |
| DIN EN ISO 19490:2016-07 (Draft) | Identical |
| NEN EN ISO 19490 : 2017 | Identical |
| NS EN ISO 19490 : 2017 | Identical |
| PN EN ISO 19490 : 2017 | Identical |
| BS EN ISO 19490:2017 | Identical |
| EN ISO 19490:2017 | Identical |
| I.S. EN ISO 19490:2017 | Equivalent |
| DS EN ISO 19490 : 2017 | Identical |
| UNE-EN ISO 19490:2018 | Identical |
| I.S. EN ISO 19490:2017 | Identical |
| NF EN ISO 19490 : 2017 | Identical |
| ISO 6507-1:2005 | Metallic materials — Vickers hardness test — Part 1: Test method |
| ISO 13504:2012 | Dentistry — General requirements for instruments and related accessories used in dental implant placement and treatment |
| ISO 6508-1:2016 | Metallic materials — Rockwell hardness test — Part 1: Test method |
| ISO 1942:2009 | Dentistry — Vocabulary |
| ISO 15087-1:1999 | Dental elevators — Part 1: General requirements |
| ISO 16443:2014 | Dentistry — Vocabulary for dental implants systems and related procedure |
| 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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