EN ISO 10993-11:2018
Current
Current
The latest, up-to-date edition.
Biological evaluation of medical devices - Part 11: Tests for systemic toxicity (ISO 10993-11:2017)
Published date
30-05-2018
Publisher
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ISO 10993-11:2017 specifies requirements and gives guidance on procedures to be followed in the evaluation of the potential for medical device materials to cause adverse systemic reactions.
| Committee |
CEN/TC 206
|
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Current
|
| Supersedes |
| Standards | Relationship |
| DS/EN ISO 10993-11:2018 | Identical |
| DIN EN ISO 10993-11:2018-09 | Identical |
| NF EN ISO 10993-11 : 2018 | Identical |
| NEN-EN-ISO 10993-11 : 2018 | Identical |
| ÖNORM EN ISO 10993-11:2025 04 15 | Identical |
| ISO 10993-11:2017 | Identical |
| I.S. EN ISO 10993-11:2018 | Identical |
| SS-EN ISO 10993-11:2018 | Identical |
| PN-EN ISO 10993-11 : 2018 | Identical |
| BS EN ISO 10993-11:2018 | Equivalent |
| BS EN ISO 10993-11:2018 | Identical |
| UNE-EN ISO 10993-11:2018 | Identical |
Summarise
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