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Standards ÖNORM - Austrian standards - Page 2143
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 11607-1
WITHDRAWN
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Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006)
WITHDRAWN published on 1.6.2007
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ÖNORM EN ISO 11607-1
WITHDRAWN
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Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006)
WITHDRAWN published on 1.7.2006
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ÖNORM EN ISO 11607-1
WITHDRAWN
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Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2006+Amd 1:2014) (consolidated version)
WITHDRAWN published on 15.11.2014
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ÖNORM EN ISO 11607-1
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Packaging for terminally sterilized medical devices - Part 1: Requirements for materials, sterile barrier systems and packaging systems (ISO 11607-1:2019)
WITHDRAWN published on 15.4.2020
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ÖNORM EN ISO 11607-2
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Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006, including Amd 1:2014)
WITHDRAWN published on 1.4.2018
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ÖNORM EN ISO 11607-2
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Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006)
WITHDRAWN published on 1.7.2006
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ÖNORM EN ISO 11607-2
WITHDRAWN
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Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2006 + Amd 1:2014) (consolidated version)
WITHDRAWN published on 15.11.2014
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ÖNORM EN ISO 11607-2
WITHDRAWN
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Packaging for terminally sterilized medical devices - Part 2: Validation requirements for forming, sealing and assembly processes (ISO 11607-2:2019)
WITHDRAWN published on 15.4.2020
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ÖNORM EN ISO 11608-1
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Needle-based injection systems for medical use - Requirements and test methods - Part 1: Needle-based injection systems (ISO 11608-1:2012)
WITHDRAWN published on 1.12.2012
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ÖNORM EN ISO 11608-1
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Pen-injectors for medical use - Part 1: Pen-injectors - Requirements and test methods (ISO 11608-1:2000)
WITHDRAWN published on 1.3.2001
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