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.
Tags
Organization
Country / Region
European Union
License
Creative Commons Attribution 4.0