UNE-EN ISO 10993-6:2017
Current
Current
The latest, up-to-date edition.
Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016)
Available format(s)
Hardcopy , PDF
Language(s)
Spanish, Castilian, English
Published date
25-10-2017
Publisher
Important note : All end users must be registered with an Account prior to user licenses being assigned.| Committee |
CTN 111
|
| DevelopmentNote |
Supersedes UNE EN 30993-6. (10/2007)
|
| DocumentType |
Standard
|
| Pages |
47
|
| PublisherName |
Asociacion Espanola de Normalizacion
|
| Status |
Current
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| ISO 10993-6:2016 | Identical |
| NBN EN ISO 10993-6 : 2009 | Identical |
| NEN EN ISO 10993-6 : 2016 | Identical |
| NS EN ISO 10993-6 : 2016 | Identical |
| I.S. EN ISO 10993-6:2016 | Identical |
| SN EN ISO 10993-6 : 2017 | Identical |
| UNI EN ISO 10993-6 : 2009 | Identical |
| BS EN ISO 10993-6:2016 | Identical |
| EN ISO 10993-6:2016 | Identical |
| NF EN ISO 10993-6 : 2017 | Identical |
| DIN EN ISO 10993-6:2009-08 | Identical |
| DIN EN ISO 10993-6:2017-09 | Identical |
| ISO 10993-4:2017 | Biological evaluation of medical devices — Part 4: Selection of tests for interactions with blood |
| ISO 10993-16:2017 | Biological evaluation of medical devices — Part 16: Toxicokinetic study design for degradation products and leachables |
| ISO 10993-2:2006 | Biological evaluation of medical devices — Part 2: Animal welfare requirements |
| ISO 10993-12:2012 | Biological evaluation of medical devices Part 12: Sample preparation and reference materials |
| ISO 10993-1:2009 | Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
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