Verification of manufactured class D IVDs by notified bodies

Name: Verification of manufactured class D IVDs by notified bodies
Creator: European Commission
License: https://creativecommons.org/licenses/by/4.0/
Keywords: class-d,diagnostics,guidances,in-vitro-diagnostic-medical-devices,in-vitro-diagnostics,ivd,ivdmd,ivds,mdcg,medical-devices,notified-bodies

Information

Type

Guidance

Regulated products

IVDMD, Medical Devices

Topics

In Vitro Diagnostic Medical Devices (IVD)

Published

February 1, 2022

Last updated

February 1, 2022

Description

This document discusses the verification process for class D IVDs by notified bodies, focusing on in vitro diagnostic medical devices (IVD).

Organization

European Commission 🇪🇺

Country / Region

European Union

License

Creative Commons Attribution 4.0

Feedback

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1 Main file

MDCG 2022-3

Updated on September 6, 2023

pdf

URL: https://health.ec.europa.eu/document/download/ebbc4f6a-4945-4d5d-9c22-9bc1aafc5532_en?filename=mdcg_2022-3_en.pdf
Permalink: https://data.openrid.co/en/datasets/r/3923678e-588f-403a-bfee-ab3e6011923d
MIME Type: application/pdf

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