• Shopping Cart
    There are no items in your cart

EN ISO 18113-3:2024

Current

Current

The latest, up-to-date edition.

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2022)

Published date

12-06-2024

Sorry this product is not available in your region.

This document specifies requirements for information supplied by the manufacturer of in vitro diagnostic (IVD) instruments intended for professional use.This document also applies to apparatus and equipment intended to be used with IVD instruments for professional use.This document can also be applicable to accessories.This document does not apply to:a) instructions for instrument servicing or repair;b) IVD reagents, including calibrators and control materials for use in control of the reagent;c) IVD instruments for self-testing.

DocumentType
Standard
PublisherName
Comite Europeen de Normalisation
Status
Current

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.