We use cookies to make our websites more user-friendly and to continuously improve them. If you continue to use the website, you consent to the use of cookies. You can find more information in our privacy statement and our cookie guidelines.

Dear Customer

Our Customer Service will be available again as of 2 January 2025. 

Please note that new registrations and requests to be processed manually will only be processed from this point onwards.

You can of course place orders and receive downloads online at any time.

We wish you happy holidays, a peaceful time and a healthy New Year!

Your DIN Media

Standards Worldwide
Standards Worldwide
Phone +49 30 58885700-07

Standard [WITHDRAWN]

DIN EN ISO 18113-3:2013-01

In vitro diagnostic medical devices - Information supplied by the manufacturer (labelling) - Part 3: In vitro diagnostic instruments for professional use (ISO 18113-3:2009); German version EN ISO 18113-3:2011

German title
In-vitro-Diagnostika - Bereitstellung von Informationen durch den Hersteller - Teil 3: Geräte für in-vitro-diagnostische Untersuchungen zum Gebrauch durch Fachpersonal (ISO 18113-3:2009); Deutsche Fassung EN ISO 18113-3:2011
Publication date
2013-01
Original language
German
Pages
18

from 77.90 EUR VAT included

from 72.80 EUR VAT excluded

Format and language options

PDF download 1

  • 77.90 EUR

  • 93.50 EUR

  • 97.50 EUR

Shipment (3-5 working days) 1

  • 94.00 EUR

  • 117.80 EUR

Monitor with the Standards Ticker

1

 Attention: Document withdrawn!

Easily subscribe: Save time and money now!

You can also subscribe to this document - together with other important standards in your industry. This makes your work easier and pays for itself after a short time.

Sparschwein_data
Subscription advantages
Sparschwein Vorteil 1_data

Important standards for your industry, regularly updated

Sparschwein Vorteil 2_data

Much cheaper than buying individually

Sparschwein Vorteil 3_data

Useful functions: Filters, version comparison and more

Publication date
2013-01
Original language
German
Pages
18
DOI
https://dx.doi.org/10.31030/1923432

Product information on this site:

Quick delivery via download or delivery service

Buy securely with a credit card or pay upon receipt of invoice

All transactions are encrypted

Overview

The revised standard includes a more precise version of Annex ZA, which presents the relationship between the European Standard and the essential requirements of the EU Directive 98/79/EC on in vitro diagnostic medical devices.

Content
ICS
11.100.10
DOI
https://dx.doi.org/10.31030/1923432
Replacement amendments

This document replaces DIN EN ISO 18113-3:2010-05 .

This document has been replaced by: DIN EN ISO 18113-3:2024-10 .

Cooperation at DIN

Also available in
Relationship to other standards
This document references:
This document is referenced in:
Loading recommended items...
Loading recommended items...
Loading recommended items...
Loading recommended items...