DS/EN ISO 18113-1:2024
Current
Current
The latest, up-to-date edition.
In vitro diagnostic medical devices– Information supplied by the manufacturer (labelling)– Part1:Terms, definitions, and general requirements (ISO 18113-1:2022)
Published date
19-06-2024
Publisher
This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.
Sorry this product is not available in your region.
Access your standards online with a subscription
Features
-
Simple online access to standards, technical information and regulations.
-
Critical updates of standards and customisable alerts and notifications.
-
Multi-user online standards collection: secure, flexible and cost effective.