SS-EN ISO 18113-2:2024
Current
Current
The latest, up-to-date edition.
In vitro diagnostic medical devices — Information supplied by the manufacturer (labelling) — Part 2: In vitro diagnostic reagents for professional use (ISO 18113-2:2022, IDT)
Available format(s)
Hardcopy
Language(s)
English
Published date
02-09-2024
Publisher
This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents, calibrators and controls intended for professional use.
Committee |
ISO/TC 212
|
DocumentType |
Standard
|
Pages |
28
|
PublisherName |
Standardiserings-Kommissionen I Sverige
|
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.