ISO 18113-1

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ISO 18113-1:2022

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

USD 215.00

This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.

This document does not address language requirements since that is the domain of national laws and regulations.

This document does not apply to:

a) IVD medical devices for performance evaluation (e.g. for investigational use only);

b) shipping documents;

c) material safety data sheets / Safety Data Sheets;

d) marketing information (consistent with applicable legal requirements).

Standard Number ISO 18113-1:2022
Title ISO 18113-1:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements
Status Published
Publication Date 06 Oct 2022
Committee ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems
Publisher PECB Store
Format PDF
Pages 53
Price USD 215.00
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