STANDARD
ÖNORM EN ISO 18113-2
Issue date: 2024 10 01
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022)
General information on ÖNORM EN ISO 18113-2
Timeline
An overview of the development of ÖNORM EN ISO 18113-2 from 1993 til today.
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ÖNORM EN ISO 18113-2In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2:...
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ÖNORM EN ISO 18113-2In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2:...
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ÖNORM EN ISO 18113-2In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 2:...
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ÖNORM EN 3752001 04 01 Standard ÖNORM EN 375, Edition: 2001 04 01Information supplied by the manufacturer with in vitro diagnostic reagents for professional use
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ÖNORM EN 3751993 03 01 Standard ÖNORM EN 375, Edition: 1993 03 01In vitro diagnostic systems - Requirements for labelling of in vitro diagnostic reagents for profess...
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Normative References
Here you will find an extract of the normative references. Please refer to the document itself for the full list.
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