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Homepage>ISO Standards>ISO 18113-1:2009-In vitro diagnostic medical devices-Information supplied by the manufacturer (labelling)-Part 1: Terms, definitions and general requirements
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download between 0-24 hoursReleased: 2009
ISO 18113-1:2009-In vitro diagnostic medical devices-Information supplied by the manufacturer (labelling)-Part 1: Terms, definitions and general requirements

ISO 18113-1:2009

In vitro diagnostic medical devices

CURRENCY
180 EUR
Standard´s number:ISO 18113-1:2009
Pages:49
Edition:1
Released:2009
Language:English
DESCRIPTION

ISO 18113-1:2009


ISO 18113-1:2009 defines concepts, establishes general principles and specifies essential requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) medical devices.
Replacements

ISO 18113-1:2022-In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling)-Part 1: Terms, definitions, and general requirements
ISO 18113-1:2022-In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling)-Part 1: Terms, definitions, and general requirements

English PDF
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English Hardcopy
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French PDF
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French Hardcopy
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