Comment Closes On
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Committee
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CH/172/7 |
Document Type
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Draft |
ISBN
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Pages
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Published
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|
Publisher
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British Standards Institution
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Status
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Superseded |
Superseded By
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ISO 10993-3:2014
|
Biological evaluation of medical devices — Part 3: Tests for genotoxicity, carcinogenicity and reproductive toxicity |
ISO 10993-13:2010
|
Biological evaluation of medical devices Part 13: Identification and quantification of degradation products from polymeric medical devices |
ISO 10993-2:2006
|
Biological evaluation of medical devices — Part 2: Animal welfare requirements |
ISO 11979-3:2012
|
Ophthalmic implants — Intraocular lenses — Part 3: Mechanical properties and test methods |
ISO 10993-10:2010
|
Biological evaluation of medical devices Part 10: Tests for irritation and skin sensitization |
ISO 10993-11:2017
|
Biological evaluation of medical devices — Part 11: Tests for systemic toxicity |
ISO 10993-12:2012
|
Biological evaluation of medical devices Part 12: Sample preparation and reference materials |
ISO 11979-1:2006
|
Ophthalmic implants Intraocular lenses Part 1: Vocabulary |
ISO 10993-1:2009
|
Biological evaluation of medical devices Part 1: Evaluation and testing within a risk management process |
ISO 3696:1987
|
Water for analytical laboratory use — Specification and test methods |
ISO 11979-2:2014
|
Ophthalmic implants — Intraocular lenses — Part 2: Optical properties and test methods |
ISO 14971:2007
|
Medical devices Application of risk management to medical devices |
ISO 10993-6:2016
|
Biological evaluation of medical devices Part 6: Tests for local effects after implantation |
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