ISO 24884:2026

Electronic instructions for use for in vitro diagnostic medical devices — Minimum required information and means of delivery

Publication date:   Sep 7, 2026

General information

60.60   Standard published   Sep 7, 2026

ISO

ISO/TC 212 Clinical laboratory testing and in vitro diagnostic test systems

International Standard

11.100.10   In vitro diagnostic test systems

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Scope

This document provides requirements and recommendations on the conditions (means of delivery) and minimum required information to deliver when providing electronic instructions for use (eIFU) for in vitro diagnostic medical devices (IVDs).
The content of the eIFU is not in the scope of this standard, as it is covered by the documents in the ISO 18113 series.

Life cycle

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PUBLISHED
ISO 24884:2026
60.60 Standard published
Sep 7, 2026