Legacy devices
Information
Type
Miscellaneous
Regulated products
IVDMD, Medical Devices
Topics
Medical Device Industry
Last updated
February 28, 2024
Description
Regulation (EU) 2017/745, for medical devices, and Regulation (EU) 2017/746, for in vitro diagnostic medical devices, allow CE-marked devices under the previous directives to remain on the market in some particular cases.
Tags
Organization
Country / Region
Italy
License
Creative Commons Attribution 3.0