Comment Closes On
|
|
Committee
|
CH/194 |
Document Type
|
Draft |
ISBN
|
|
Pages
|
|
Published
|
|
Publisher
|
British Standards Institution
|
Status
|
Superseded |
Superseded By
|
|
ISO 14155-2:2003
|
Clinical investigation of medical devices for human subjects Part 2: Clinical investigation plans |
ISO 10993-13:2010
|
Biological evaluation of medical devices Part 13: Identification and quantification of degradation products from polymeric medical devices |
ISO 14155-1:2003
|
Clinical investigation of medical devices for human subjects Part 1: General requirements |
ISO 10993-2:2006
|
Biological evaluation of medical devices — Part 2: Animal welfare requirements |
ISO 10993-14:2001
|
Biological evaluation of medical devices Part 14: Identification and quantification of degradation products from ceramics |
ISO 10993-18:2005
|
Biological evaluation of medical devices Part 18: Chemical characterization of materials |
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 |
ISO 10993-9:2009
|
Biological evaluation of medical devices Part 9: Framework for identification and quantification of potential degradation products |
ISO 10993-6:2016
|
Biological evaluation of medical devices Part 6: Tests for local effects after implantation |
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