Application of transitional provisions for certification of class D in vitro diagnostic medical devices according to Regulation (EU) 2017/746

Name: Application of transitional provisions for certification of class D in vitro diagnostic medical devices according to Regulation (EU) 2017/746
Creator: European Commission
License: https://creativecommons.org/licenses/by/4.0/
Keywords: applications,certification,class-d,diagnostics,eu,european-union,guidances,in-vitro-diagnostic-medical-devices,in-vitro-diagnostics,ivd,ivdmd,ivds,mdcg,medical-devices,provisions,regulations

Information

Type

Guidance

Regulated products

IVDMD, Medical Devices

Topics

In Vitro Diagnostic Medical Devices (IVD)

Published

April 1, 2021

Last updated

April 1, 2021

Description

This document discusses the application of transitional provisions for certifying class D in vitro diagnostic medical devices under Regulation (EU) 2017/746.

Organization

European Commission 🇪🇺

Country / Region

European Union

License

Creative Commons Attribution 4.0

Feedback

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1 Main file

MDCG 2021-4

Updated on September 6, 2023

pdf

URL: https://health.ec.europa.eu/document/download/9f23fca0-f407-4e45-a464-2d71b575d1fe_en?filename=mdcg_2021-4_en.pdf
Permalink: https://data.openrid.co/en/datasets/r/186ea0fe-160b-4ba7-b582-d185589ee65e
MIME Type: application/pdf

Created on: September 6, 2023
Modified on: September 6, 2023