ÖNORM - Rakúske normy - Stránka 3038

ÖNORM EN ISO 18104 (01.06.2014) Neplatné

Health informatics - Categorial structures for representation of nursing diagnoses and nursing actions in terminological systems (ISO 18104:2014)

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ÖNORM EN 1811 (01.02.1999) Neplatné

Reference test method for release of nickel from products intended to come into direct and prolonged contact with the skin

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ÖNORM EN 1811 (01.08.2008) Neplatné

Reference test method for release of nickel from products intended to come into direct and prolonged contact with the skin

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ÖNORM EN 1811 (15.10.2015) Neplatné

Reference test method for release of nickel from all post assemblies which are inserted into pierced parts of the human body and articles intended to come into direct and prolonged contact with the skin

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ÖNORM EN 1811 (15.04.2011) Neplatné

Reference test method for release of nickel from all post assemblies which are inserted into pierced parts of the human body and articles intended to come into direct and prolonged contact with the skin

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ÖNORM EN 1811 (15.08.2012) Neplatné

Reference test method for release of nickel from all post assemblies which are inserted into pierced parts of the human body and articles intended to come into direct and prolonged contact with the skin (consolidated version)

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ÖNORM EN 1811 (15.09.2015) Neplatné

Reference test method for release of nickel from all post assemblies which are inserted into pierced parts of the human body and articles intended to come into direct and prolonged contact with the skin

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ÖNORM EN ISO 18113-1 (01.12.2012) Neplatné

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)

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ÖNORM EN ISO 18113-1 (15.04.2010) Neplatné

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions and general requirements (ISO 18113-1:2009)

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ÖNORM EN ISO 18113-2 (01.12.2012) Neplatné

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2009)

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