prSSH ISO 18113-3:2022

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

General information

Current stage: 40.20 Effective date: Feb 3, 2023

Next stage: 40.60 Next stage date: May 3, 2023

Originator: DPS

Owner: DPS/KT 140

Type: International Standard

ICS: 11.100.10

Scope

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.

Life cycle

NOW

IN_DEVELOPMENT
prSSH ISO 18113-3:2022
40.20 DIS ballot initiated: 12 weeks
Feb 3, 2023

Preview

Only informative sections of projects are publicly available. To view the full content, you will need to members of the committee. If you are a member, please log in to your account by clicking on the "Log in" button.