In vitro diagnostic medical devices - Provision of information by the manufacturer (labelling) - Part 3: Equipment for in vitro diagnostic studies for use by professionals (ISO 18113-3:2022)

Available format(s)

Hardcopy

Language(s)

German - English

Published date

01-10-2024

Publisher

Osterreichisches Normungsinstitut/Austrian Standards

€147.32

Excluding VAT

This document specifies requirements for the information provided by the manufacturer of in vitro diagnostic (IVD) equipment for use by qualified personnel.

Committee	ISO/TC 212
DocumentType	Standard
Pages	23
PublisherName	Osterreichisches Normungsinstitut/Austrian Standards
Status	Current
Supersedes	ONORM EN ISO 18113-3 : 2012

Standards	Relationship
ISO 18113-3:2022	Identical
EN ISO 18113-3:2024	Identical

Summarise

ChatGPT Perplexity

Access your standards online with a subscription

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.

Get in touch with us

€147.32

Excluding VAT

Product format

I agree to the DRM document license rules apply against the PDF selection made.

Please confirm that you agree to the document license rules for this document.

I agree to the document license rules .

Please confirm that you agree to the document license rules for this document.

Shopping Cart

ÖNORM EN ISO 18113-3:2024 10 01

In vitro diagnostic medical devices - Provision of information by the manufacturer (labelling) - Part 3: Equipment for in vitro diagnostic studies for use by professionals (ISO 18113-3:2022)

Shopping Cart

ÖNORM EN ISO 18113-3:2024 10 01

In vitro diagnostic medical devices - Provision of information by the manufacturer (labelling) - Part 3: Equipment for in vitro diagnostic studies for use by professionals (ISO 18113-3:2022)

Abstract

General Product Information

International Equivalents

Industry

Sub-Industry