In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)

Available format(s)

Hardcopy

Language(s)

English - French

Published date

01-06-2024

Publisher

Swiss Standards

This document defines concepts, establishes general principles, and specifies essential requirements for information supplied by the manufacturer of IVD medical devices.

Committee	INB/NK 157
DocumentType	Standard
Pages	0
PublisherName	Swiss Standards
Status	Current
Supersedes	SN EN ISO 18113-1 : 2012

Standards	Relationship
ISO 18113-1:2022	Identical
EN ISO 18113-1:2024	Identical

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SN EN ISO 18113-1:2024

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 1: Terms, definitions, and general requirements (ISO 18113-1:2022)

Abstract

General Product Information

International Equivalents

Category

Subcategory