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Standards ÖNORM - Austrian standards - Page 2091
In Austria, around 4,000 experts in active committees develop standards for the domestic, European and global market. They represent the interests of the economy, consumers, research, administration and society.
Together with them, Austrian Standards – the Austrian competence centre for standards – finds solutions ensuring that everything fits together perfectly and life runs smoothly. Austrian Standards distributes know-how laid down in standards as quickly as possible so that people and the economy can profit from it.
Austrian Standards, established in 1920, is structured in the business divisions of development, consulting, publishing, training and certification and finances the standardization system by more than 80 per cent through the sale of its products and services. Its legal basis is defined in the Standardization Act (Normengesetz 2016).
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ÖNORM EN ISO 10993-4
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Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002)
WITHDRAWN published on 1.4.2003
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ÖNORM EN ISO 10993-4
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Biological evaluation of medical devices - Part 4: Selection of tests for interactions with blood (ISO 10993-4:2002, including Amd 1:2006)
WITHDRAWN published on 15.8.2009
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ÖNORM EN ISO 10993-5
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Biological evaluation of medical devices - Part 5: Tests for in vitro cytotoxicity (ISO 10993-5:1999)
WITHDRAWN published on 1.12.1999
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ÖNORM EN ISO 10993-6
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Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)
WITHDRAWN published on 1.8.2007
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ÖNORM EN ISO 10993-6
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Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2016)
WITHDRAWN published on 15.6.2017
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ÖNORM EN ISO 10993-6
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Biological evaluation of medical devices - Part 6: Tests for local effects after implantation (ISO 10993-6:2007)
WITHDRAWN published on 15.9.2009
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ÖNORM EN ISO 10993-7
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Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:1995)
WITHDRAWN published on 1.1.1996
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ÖNORM EN ISO 10993-7
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Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008)
WITHDRAWN published on 1.2.2009
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ÖNORM EN ISO 10993-7
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Biological evaluation of medical devices - Part 7: Ethylene oxide sterilization residuals (ISO 10993-7:2008 + Cor 1:2009) (consolidated version)
WITHDRAWN published on 15.12.2010
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ÖNORM EN ISO 10993-8
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Biological evaluation of medical devices - Part 8: Selection and qualification of reference materials for biological tests (ISO 10993-8:2000)
WITHDRAWN published on 1.12.2000
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