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KS ISO 10993-13:1998

Biological evaluation of medical devices - Part 13: Identification and quantification of degradation products from polymeric medical devices.

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Kes 3,038.00

KS ISO 10993-14:2001

Biological evaluation of medical devices - Part 14: Identification and quantification of degradation products from ceramics.

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Kes 3,038.00

KS ISO 10993-15:2019

Biological evaluation of medical devices - Part 15: Identification and quantification of degradation products from metals and alloys.

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Kes 3,167.00

KS ISO 10993-16:2017

Biological evaluation of medical devices - Part 16: Toxicokinetic study design for degradation products and leachables.

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Kes 3,167.00

KS ISO 10993-17:2002

Biological evaluation of medical devices - Part 17: Establishment of allowable limits for leachable substances.

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Kes 3,605.00

KS ISO 10993-2:1992

Biological evaluation of medical devices - Part 2: Animal welfare requirements.

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Kes 2,472.00

KS ISO 10993-4:2017

Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood

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Kes 5,562.00

KS ISO 10993-5:1999

Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity.

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Kes 2,884.00

KS ISO 10993-6:1994

Biological evaluation of medical devices - Part 6: Tests for local effects after implantation.

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Kes 3,038.00

KS ISO 10993-9:2019

Biological evaluation of medical devices - Part 9: Framework for identification and quantification of potential degradation products.

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Kes 3,038.00

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