EN ISO 18113-4:2024
Current
The latest, up-to-date edition.
In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 4: In vitro diagnostic reagents for self-testing (ISO 18113-4:2022)
12-06-2024
This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) reagents, calibrators, and controls intended for self-testing.This document can also be applicable to accessories.This document is applicable to the labels for outer and immediate containers and to the instructions for use.This document does not apply to:a) IVD instruments or equipment;b) IVD reagents for professional use.
| DocumentType |
Standard
|
| PublisherName |
Comite Europeen de Normalisation
|
| Status |
Current
|
| Standards | Relationship |
| ÖNORM EN ISO 18113-4:2024 10 01 | Identical |
| UNI EN ISO 18113-4:2024 | Identical |
| SS-EN ISO 18113-4:2024 | Identical |
| DS/EN ISO 18113-4:2024 | Identical |
| NF EN ISO 18113-4:2024 | Identical |
| SN EN ISO 18113-4:2024 | 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.