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Product Product ISO 18113-1:2022
Price Price USD 215.00
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Description Description

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 Standard Number ISO 18113-1:2022
Title Title ISO 18113-1:2022 In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 1: Terms, definitions, and general requirements
Status Status Published
Publication Date Publication Date 06 Oct 2022
Cross References Cross References
Descriptors Descriptors
ICS ICS 11.100.10
Committee Committee ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems
ISBN ISBN
Publisher Publisher PECB Store
Format Format PDF
Delivery Delivery NO
Pages Pages 53
File Size File Size KB