DS/EN ISO 18113-2:2024
Current
Current
The latest, up-to-date edition.
In vitro diagnostic medical devices– Information supplied by the manufacturer (labelling)– Part2:In vitro diagnostic reagents for professional use (ISO 18113-2:2022)
Published date
19-06-2024
Publisher
Sorry this product is not available in your region.
This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents, calibrators and controls intended for professional use.
Committee |
DS/S-260
|
DocumentType |
Standard
|
PublisherName |
Danish Standards
|
Status |
Current
|
Supersedes |
Standards | Relationship |
ISO 18113-2:2022 | Identical |
EN ISO 18113-2:2024 | Identical |
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.