BS EN ISO 10993-11:2009
Withdrawn
Withdrawn
View Superseded by
Biological evaluation of medical devices Tests for systemic toxicity
Available format(s)
Hardcopy , PDF
Language(s)
English
Published date
06-30-2009
Publisher
Withdrawn date
10-27-2018
Superseded by
US$400.07
Excluding Tax where applicable
| Committee |
CH/194
|
| DevelopmentNote |
Supersedes 94/504043 DC, BS 5736-3(1981) & BS 5736-5(1982). (11/2005)
|
| DocumentType |
Standard
|
| Pages |
38
|
| PublisherName |
British Standards Institution
|
| Status |
Withdrawn
|
| SupersededBy | |
| Supersedes |
| Standards | Relationship |
| NEN EN ISO 10993-11 : 2009 | Identical |
| NBN EN ISO 10993-11 : 2009 | Identical |
| NS EN ISO 10993-11 : 2009 | Identical |
| EN ISO 10993-11:2009 | Identical |
| DIN EN ISO 10993-11:2015-12 (Draft) | Identical |
| ISO 10993-11:2017 | Identical |
| NF EN ISO 10993-11 : 2009 | Identical |
| I.S. EN ISO 10993-11:2009 | Identical |
| DIN EN ISO 10993-11:2009-08 | Equivalent |
| UNE-EN ISO 10993-11:2009 | Identical |
| DIN EN ISO 10993-11:2009-08 | Identical |
| BS EN 1283:1996 | Haemodialysers, haemodiafilters, haemofilters, haemoconcentrators and their extracorporeal circuits |
| 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 |
| ASTM F 619 : 2014 : REDLINE | Standard Practice for Extraction of Medical Plastics |
| ISO 10993-1:2009 | Biological evaluation of medical devices — Part 1: Evaluation and testing within a risk management process |
Summarise
US$400.07
Excluding Tax where applicable
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