Guidance on appropriate surveillance regarding the transitional provisions under Article 110 of the IVDR with regard to devices covered by certificates according to the IVDD

Information

Type

Guidance

Regulated products

IVDMD, Medical Devices

Topics

In Vitro Diagnostic Medical Devices (IVD)

Published

September 1, 2022

Last updated

September 1, 2022

Description

Guidance on surveillance for transitional provisions under Article 110 of the IVDR for devices covered by IVDD certificates.

Organization

Country / Region

European Union

License

Creative Commons Attribution 4.0

Feedback

Suggest an improvement to this page

Actions

Social networks

Embed