• Shopping Cart
    There are no items in your cart

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

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.